Yeast whole genome sequencing (WGS) lacks end-to-end workflows that identify genetic engineering. Here we present Prymetime, a tool that assembles yeast plasmids and chromosomes and annotates genetic engineering sequences. It is a hybrid workflow—it uses short and long reads as inputs to perform separate linear and circular assembly steps. This structure is necessary to accurately resolve genetic engineering sequences in plasmids and the genome. We show this by assembling diverse engineered yeasts, in some cases revealing unintended deletions and integrations. Furthermore, the resulting whole genomes are high quality, although the underlying assembly software does not consistently resolve highly repetitive genome features. Finally, we assemble plasmids and genome integrations from metagenomic sequencing, even with 1 engineered cell in 1000. This work is a blueprint for building WGS workflows and establishes WGS-based identification of yeast genetic engineering.
Complete and accurate detection of genetic engineering is needed to validate strain engineering, protect intellectual property, monitor for release events, and detect engineered organisms in unknown samples. Whole genome sequencing (WGS) is an attractive detection method because it does not depend on specific sequence features and captures all sequences – including intended and unintended modifications. Yet, precise resolution of genetic engineering places strict requirements on a WGS workflow – genetic engineering signatures must be clearly identified within accurate, complete, and contiguous sequences.
Thus, a WGS workflow is needed for engineered organisms. In this work, we focus particularly on engineered yeasts. Yeasts are a crucial testbed for genome-scale design1,2, and accurate WGS will be necessary for validating synthesized eukaryotic genomes. Yeast are also cell factories for medicines3,4, fuels5,6, materials7,8, and chemicals9,10. These are derived from several species of baker’s yeast Saccharomyces cerevisiae11,12,13 and nonconventional yeasts like Yarrowia lipolytica14,15,16 and Komagataella phaffii (formerly Pichia pastoris)17,18. Given the economic importance and increasing use of engineered yeast cell factories, it is crucial that WGS methods are developed that can efficiently validate the presence of intended engineering and confirm the absence of unintended variation. Without WGS, the majority of yeast strains are currently validated with less comprehensive methods like PCR and targeted sequencing. These methods do not capture the unintended secondary mutations common in engineered organisms19,20,21,22,23. There are also many unpublished accounts of WGS revealing unexpected sequences and genome structures in engineered industrial strains. Taken together, this evidence challenges the assumption that an observed phenotype is the direct result of intended engineering, illuminating a possible explanation for variation between replicates and irreproducible findings – a common problem for biology-related disciplines24. Clearly, WGS must be used more broadly to detect and validate genetic engineering in yeasts.
Yeast engineering leaves many predictable sequence features in the genome, like standard plasmid sets with known replication origins and expression parts25,26,27,28, integrations29,30,31,32, gene knockouts33, and genome edits using RNA-guided endonucleases34,35,36,37,38,39. Many of these can be identified in a genome sequence with a tool such as BLAST40. Yet, engineered yeast present several obstacles to complete, accurate genome assembly. The high sequence identity in many engineered constructs, such as common plasmid elements or parts derived from the host genome, can cause identical sequences to be omitted41,42. Engineered yeast also have complex genome features like multiple deletions13, multiple plasmids with varying copy numbers30, many insertions36, and SCRaMbLEd chromosomes43,44. Furthermore, the scale of yeast engineering is increasing both in the fraction of a genome that may be rewritten45,46, and in the numbers of engineered strains created through adaptive laboratory evolution47,48,49 and combinatorial pathway engineering50,51,52,53,54. These iterative approaches result in many strains that are costly to sequence. These obstacles are in addition to typical complexities like naturally repetitive regions (telomeres and ribosomal DNA), rearrangements, and polyploidy. Each make accurate, complete, and contiguous yeast genomes difficult to attain without a significant allocation of resources.
A WGS workflow consists of five steps: DNA isolation, library preparation, sequencing, assembly, and annotation. First, genomic DNA is purified using one of a variety of methods, including phenol-choloroform, bead beating, or enzymatic lysis55. Second, the sequencing library is prepared by attaching adapters and barcodes. This can be done via ligation, which involves shearing the DNA to create free ends for DNA ligase to attach adapters, or tagmentation, which randomly inserts adapter attachment points without shearing56. Third, the library is sequenced with a next-generation sequencing (NGS) platform that either generates short reads (150–300 base pairs long) with high nucleotide accuracy56 or long reads (1.5 kilobases to megabases long) with lower accuracy57. The average read length and the number of reads (genome coverage) output by the NGS platform is dependent on sequencing technology and the preceding DNA isolation and adapter attachment steps58. Fourth, the reads are computationally assembled into a final genome sequence with software that uses either an overlap-layout-consensus (OLC) or De Bruijn graph (DBG) algorithm59. OLC and DBG assemblers are further classified into short read only, hybrid (both short and long reads), or long read with error correction. Both hybrid and long read with error correction assembly approaches currently hold the most promise to achieve accurate genome sequence and structure at low read depths, primarily because two independent technologies validate basecalls. However, this entails the use of two sequencing technologies, thereby increasing costs and time. Fifth, an annotation is performed. Eukaryotic annotation involves first predicting genes in the genome sequence, followed by functional annotation60. However, features like genetic engineering parts, telomeres, centromeres, mitochondrial DNA, and natural plasmids are often not annotated, and several are by convention not included in the final assembly.
In this work, we develop an inexpensive WGS workflow designed to detect genetic engineering in pure and mixed samples of engineered yeast. To accomplish this, we optimized each of the five steps in the WGS workflow in order to correctly resolve all engineering sequences in a heavily engineered yeast strain. We first improved DNA isolation and sequencing library preparation to increase representation of reads from circular DNA molecules. We then used a combination of long- and short-read sequencing from inexpensive sequencing platforms to achieve high coverage at low cost. We integrated two different assemblers to resolve both circular plasmids and linear chromosomes accurately. We developed an annotation approach based on a user-input list of genetic parts to clearly identify common signatures of engineering. Using this approach, we also annotated centromeres, telomeres, origins of replication, and mitochondrial DNA in order to put observed genetic engineering in context with the rest of the genome. The resulting workflow is named Prymetime, "Pipeline for Recombinant Yeast genoMEs That Identifies Markers of Engineering." Through a variety of demonstrations, we show that Prymetime can validate genetic engineering, produce high quality whole genome sequences, and detect engineering in metagenomic samples. This tool is broadly useful for strain validation, release monitoring, protecting intellectual property, and investigating engineering in unknown samples.
Optimizing nanopore sequencing library preparation for engineered yeasts
At the beginning, we set a standard that a genome assembly workflow must be able to resolve chromosomal integrations and multiple plasmids used in yeast engineering. Therefore, we built a S. cerevisiae CEN.PK113 strain, FEY_2, containing an integrated carotenoid pathway, the native 2μ plasmid, a dCas9 plasmid, and a gRNA plasmid, shown in Fig. 1a. Initially, we prepared sequencing libraries of FEY_2 with the Oxford Nanopore Technologies (ONT) ligation kit. Sequencing these initial libraries had low average read length that varied from run to run, possibly because of differential DNA shearing during isolation. To limit this, we developed a gentle genomic DNA isolation protocol which increased average nanopore read length and reduced variance (Supplementary Figure S1). However, the sequencing results contained few reads from plasmids, as determined by comparing the average normalized mapped reads of the plasmid antibiotic selection markers to those of the ACT1 genomic locus using Minimap261. We could isolate plasmids from FEY_2 using a yeast miniprep kit, so we reasoned that the sequencing library preparation step was so gentle that it was not linearizing circular plasmids for adapter ligation. Thus, we turned to a tagmentation library preparation method, the ONT Rapid kit. The improvement in average normalized mapped plasmid reads is shown in Fig. 1b. We were reassured that the 2:1 and 20:1 marker to ACT1 read coverage ratios for each plasmid are equivalent to the approximate plasmid copy number in yeast for each origin12,62. Furthermore, tagmentation also increased the representation of other circular elements like the native 2μ plasmid and mitochondrial DNA. These results indicate that tagmentation is a key to achieving long average read lengths while also generating linear molecules from small circular DNA so that they can pass through the nanopore flow cell. Whereas tagmentation may have a slight AT sequence bias and perform poorly in extreme GC genomes, this is not the case with our yeasts. Thus, with gentle isolation and tagmentation, nanopore sequencing of FEY_2 resulted in adequate representation of plasmid reads.
Developing a de novo assembly workflow for complete, contiguous plasmids and integrations
Once we achieved appropriate read representation, we evaluated nine assembly algorithms with the stringent requirement that all chromosomes and plasmids must be complete, accurate, and contiguous. This is particularly stringent for the three plasmids in FEY_2 because they each have significant sequence identity between each other and the genome. The assemblers tested included the short-read only OLC assembler Edena63, the short-read only DBG assemblers ABySS64 and Velvet65, the hybrid OLC assembler Masurca66, hybrid DBG assembler HybridSPAdes67, the long-read OLC assemblers MiniASM68, Canu69, and SMARTdenovo70, and the long-read DBG assembler Flye71. The long-read assemblers, because of higher error rates57, only provide a "skeleton" for mapping additional reads72,73,74,75,76. Therefore, all long-read assemblies were polished with Medaka77, Racon78, and Pilon79.
We used the optimized library preparation to obtain long reads at 60X genome coverage from the ONT MinION and short reads at 125X genome coverage from the Illumina iSeq 100. This common set of reads was used by each assembler, and the resulting genome assembly was analyzed using BLASTN for the presence of the integrated pathway, both plasmids, and the native 2μ plasmid. A visual representation of the BLASTN results is shown in Fig. 1a. The engineering features were rarely complete or contiguous. The short-read only de novo assemblers ABySS, Edena, and Velvet returned a fragmented, incomplete pathway and plasmids. The hybrid assemblers SPAdes and Masurca produced more complete sequences than the short-read only assemblers, but the genome integration was fragmented, and Masurca also omitted portions of the three plasmids. The long-read de novo assemblers MiniASM, Canu, Flye, and SMARTdenovo each returned a single contiguous sequence for the genome integration, yet, MiniASM, Canu, and SMARTdenovo omitted sections of the three plasmids. Only Flye eventually returned the genome integration and each plasmid correctly in contiguous sequences.
Of the assemblies missing large portions of at least one of the three plasmids, almost all were generated with an OLC assembler. These algorithms use an All-versus-All consensus step that may discard highly identical sequences in order to reach consensus. To investigate this further, we used BLASTN at each step in the OLC-based Canu pipeline to determine when sequences were omitted. We noted that the complete low-copy plasmid was initially present before the consensus step, and was then lost in the final assembly. It seems that Canu discarded the plasmid at a certain threshold during the consensus step, likely because of high sequence identity with the other plasmids. In contrast, the DBG assemblers Flye, ABySS, and SPAdes did not omit sections of plasmids. DBG algorithms split reads into shorter k-mers followed by a Eulerian walk approach to construct contigs, thus DBG may be less prone to discarding highly identical sequences80. Though complete, the plasmid sequences from ABySS and SPAdes were fragmented, while Flye assembled each plasmid into a single contiguous sequence. This is possibly because ABySS and SPAdes are hybrid assemblers that assemble short reads first, then use long reads to piece together contigs. This makes them subject to the same pitfalls that plague short-read assemblers, in that the reads do not effectively span sequences with high identity. Thus, Flye, as a DBG assembler that assembles long reads first, produces higher contiguity and better resolution of sequences with high identity. These findings reinforce that genome assembly quality is dependent on high-quality long-read data and a de novo assembly approach.
While the plasmid contigs from Flye were complete and contiguous, they were longer than expected. Further inspection revealed that the contigs consisted of several repeats of the expected plasmid sequence. This is a common problem for long-read assemblers, as they use linear logic to merge contigs69,81. To obtain structurally representative plasmid contigs, we chose to re-assemble them with Unicycler, software that was built to assemble circular contigs from bacterial sequencing data82. To do this, we sent contigs either identified by Flye as circular or identified by mummer as repetitive to Unicycler. Reassembly of plasmids with Unicycler improved the accuracy as measured by BLASTN and length of the contigs for the three plasmids in FEY_2 (Supplementary Fig. S2).
Resolving engineering signatures in a collection of engineered yeasts
We next validated our assembly approach on a collection of engineered laboratory and nonconventional yeast. We constructed 15 strains from S. cerevisiae S288C, CEN.PK113-7D, W303-α, BY4741, BY4742, and K. phaffii ATCC 76273 (CBS 7435)83,84 and Y. lipolytica ATCC MYA-2613 (Po1f)85. Plasmids designed to construct transcriptional units for this study are described in Supplementary Fig. S3. A description of each strain is shown in Fig. 2a, with more details in Supplementary Table S1 and Supplementary Fig. S4. Engineering signatures were inserted into the genome or maintained on episomal plasmids. S. cerevisiae integrations were targeted to the HO locus26 or between NRT1 and GYP7 in chromosome XV38,51. S. cerevisiae plasmids consisted of custom TypeIIS-compatible yeast shuttle vectors with either S. cerevisiae replicon (2μ or CEN6/ARSH4). Engineering was broadly categorized into biosynthetic pathways, gene editing components, deletions, and synthetic biology elements. Biosynthetic pathways included propane86, 2β-carotene87, prespatane88, carnosic acid89, and limonene90,91. Genome editing associated tools included SpCas934, dCas935, LbCpf138, FnCpf137, and Cre recombinase33. Deletions included the synthetic auxotrophies already present in S. cerevisiae W303-α, BY4741, BY4742, and Y. lipolytica Po1f. Synthetic biology elements included fluorescent proteins92,93 and the 2A sequence94. The engineered Y. lipolytica strain "FEY_74" contained the CRISPR-Cas9 plasmid pCRISPRyl39. The engineered K. phaffii strain "FEY_75" contained a recombinase-integrated red fluorescent protein (RFP) cassette28.
We sequenced this collection with the ONT MinION and the Illumina iSeq 100 systems using our optimized library preparation protocols. The combined assembly approach using Flye and re-assembly of circular contigs with Unicycler captured each engineering signature in each S. cerevisiae genetic background as measured by BLASTN of the reference sequence against the assembly. Shown in Fig. 2a, the approach resolved seven different genome integrations in two genome loci and eleven different plasmids. The BLASTN metrics are in Supplementary Table S2. To further demonstrate the necessity of a combined assembly approach, we repeated assembly with Flye alone. The additional Unicycler step improves plasmid length and accuracy in every strain, not just FEY_2 (Supplementary Fig. S5). No sequence complexities, like the type of gene (metabolic, selective, editing, or reporter), parts identical to the genome (Ptef1, Pgal10), or plasmid copy number, affected the accuracy or structural completeness of the assemblies.
The genome assemblies from the two engineered nonconventional yeasts – Y. lipolytica strain FEY_74 and K. phaffii strain FEY_75 – revealed unintentional edits. FEY_74 was intended to contain the pCRISPR-yl plasmid39, yet the contig from the genome assembly was missing the entire Cas9 transcription unit and a portion of the E. coli origin of replication, shown in Fig. 2b. Inspection of the raw reads failed to identify a single read with the missing sequence. We performed a genomic DNA isolation and a yeast plasmid miniprep on FEY_74 and transformed the resulting DNA back into E. coli, yet did not observe any colonies. This indicates that the disrupted origin of replication in the assembly reflects an actual unintended loss rather than an assembly error. This was further confirmed by PCR of DNA isolated from FEY_74 with primers spanning the missing region of the plasmid. The length of the PCR product indicated that the sequence was indeed missing (Fig. 2b). Similarly, FEY_75 was designed to have an RFP transcription unit integrated into chromosome II (Fig. 2c). The entire pathway was found by BLASTN in the FEY_75 genome, but analysis revealed that the pathway was actually integrated into chromosome IV. This was further confirmed by PCR of the integration site in chromosome II, which was negative, yet the strain remained nourseothricin resistant and RFP positive. These results indicate that a combined assembly approach can be used to find and accurately reproduce engineering, which is useful for both strain quality control and identification of engineering in unknown samples.
Whole genome assembly quality
After achieving assembly of all engineering sequences, we then assessed whole genome quality of the 15 engineered assemblies and genomes from the parent nonconventional yeasts Y. lipolyitica Po1f and K. phaffii CBS7435. Each genome had high contiguity, sequence accuracy, and genome completeness as measured by Benchmarking Universal Single-Copy Orthologs (BUSCO) score95, calculated using the Saccharomycetales dataset (Fig. 3a) and percent aligned reads to the parent genome (Fig. 3b). Percent unmapped reads for each genome are provided in Supplementary Table S3. Whole genome alignments for each genome compared to the parent with Mauve96 are presented in Supplementary Figs. S6 and S7. The resequenced Y. lipolytica Po1f and K. phaffii CBS7435 strains were improved compared to the publicly available genomes16,84 by several metrics (Supplementary Fig. S8). Notably, there are 6 more essential genes recovered in the resequenced K. phaffii assembly and 13 more essential genes recovered in the resequenced Y. lipolytica assembly.
The final test of completeness is whether a chromosome is resolved from a telomere, through the centromere, to the other telomere. We compared each engineered S. cerevisiae assembly to its respective reference assembly to quantify the number of complete telomere-to-telomere contigs (Supplementary Fig. S9). We found that 76% of chromosomes are complete, except the telomeres. Analysis of several smaller contigs in the assemblies reveals them to be telomeric or ribosomal DNA (rDNA) sequences. This result shows that the genomes are essentially complete, save misassembly of highly repetitive genomic sequences and telomeres.
Next, we further assessed repetitive DNA elements in each S. cerevisiae genome, finding that repetitive elements like long terminal repeats (LTRs), CUP1 repeats, and rDNA are resolved with comparable copy number to the reference genomes (Fig. 3c, d, e, respectively). However, the CUP1 and rDNA repeat copy numbers were underrepresented in both our assemblies and the reference assemblies when compared to the approximate copy number of the raw Nanopore and Illumina reads. The S. cerevisiaeCUP1 copy number is highly variable, ranging from zero to 7997, while the rDNA copy number is known to range between 100 and 20098. Tandem repeats such as CUP1 and rDNA are a common problem for all de novo assemblers and are often collapsed during assembly99.
Every strain investigated in the above collection is haploid. Therefore, we sequenced the heterozygous diploid strain S. cerevisiae BY4743. The resulting assembly is similar to S. cerevisiae S288C (Fig. 4a). Thus, this assembly approach cannot resolve ploidy. However, the LYS2 and MET15 heterozygous deletions can be clearly resolved by mapping average read count (Fig. 4b, c, respectively).
Taken together, these results indicate that the genome assemblies generated by the combined assembly approach are structurally correct, accurate, and complete, although telomeres, repeat elements, and ploidy remain a challenge to accurately reproduce. This is currently a challenge in the field of de novo genome assembly.
Annotating and visualizing engineering and genome features
The last step in WGS, annotation, does not usually identify genetic engineering sequences. Therefore, we developed an engineering annotation step and applied it to the collection of 15 engineered yeasts. We first wrote an automated BLASTN script to find standard yeast genetic engineering parts and genome features. Standard parts include the CEN6/ARSH4 and 2μ replication origins, selection markers, promoters, and terminators. Genome features include centromeres, telomeres, and mitochondrial DNA, which were sourced for each parent strain from the Saccharomyces Genome Database100. This list of parts and features is simply a FASTA file, which can be easily modified and updated to find any sequence of interest in genome assemblies.
We then fed the BLASTN results to two interactive genome viewers – chromoMap101 and AliTV102. ChromoMap highlights the parts and features within each contig in the assembly. AliTV does the same, but also aligns the assembly to the parent strain using lastz103. This can highlight potential unintended changes like chromosomal rearrangements. The chromoMap visualization for FEY_2 (Fig. 5a) shows the integration in scaffold_3, and the two engineered plasmids in scaffold_18 and scaffold_23. The output is interactive, so hovering over the engineering blocks will display which parts were identified. Using this approach, the plasmids can be differentiated from other small contigs by the presence of the origins of replication and other engineering sequences. In the AliTV visualization, the high sequence identity and contiguity of the engineered as compared to unengineered S. cerevisiae CEN.PK is apparent. The AliTV visualization is also interactive and customizable, and is particularly useful to determine how contigs from the assembly align to the reference assembly.
Creating an automated pipeline
Optimization of each of the five steps of genome assembly led to a final set of methods and software that can accurately reproduce and visualize genetic engineering in highly accurate yeast genomes. We integrated each of the software steps into a single Dockerized tool that we call Prymetime, "Pipeline for Recombinant Yeast genoMEs That Identifies Markers of Engineering." The final pipeline is depicted in Fig. 5c. The software accepts long reads and short reads, and optionally accepts a list of sequences of interest and a reference genome. It outputs two interactive visualizations of the genome. Each visualization of the 15 engineered strains is depicted in Supplementary Figs. S10–S17.
As a final demonstration, we tested each step in the Prymetime workflow with a set of publicly available raw reads for S. cerevisiae CEN.PK113-7D74,104, assessing the quality at each step (Supplementary Fig. S18). First, we evaluated the contigs from Flye step, determining that 40X long-read genome coverage is sufficient to match the reference assembly. Then, we evaluated the polishing step, which demonstrated that at least 40X short-read genome coverage is needed to achieve high identity to the reference, BUSCO, and percentage of S. cerevisiae S288C CDSs (Supplementary Tables S5–S8). Using the chromoMap visualization output from Prymetime, the CEN.PK113-7D assembly correctly captures the centromeric sequences, but not the telomeric sequences (Supplementary Fig. S19). This corroborates the observations from the engineered genomes. Using different de novo assemblers still does not solve this problem (Supplementary Table S9), thus Flye remains the best underlying assembly software for assembly of accurate, complete, and contiguous genetic engineering sequences. A detailed illustration of the full Prymetime workflow is shown in Supplementary Fig. S20. These results confirm the Prymetime software workflow is as accurate as possible and show that at least 40X genome coverage for both long- and short-read sequencing data is needed to achieve the highest quality genomes.
Resolving signatures of engineering in an in silico metagenome assembly
To demonstrate a use case for Prymetime, we attempted to resolve engineering signatures in a metagenome. Publicly available reads from the Zymo mock metagenome were combined with reads from the FEY_15 strain to simulate detection of an engineered strain in a mixed sample. The mock metagenome consists of eight bacteria species – Bacillus subtilis, Enterococcus faecalis, Escherichia coli, Lactobacillus fermentum, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella enterica, and Staphylococcus aureus – and two yeast species – Cryptococcus neoformans and Saccharomyces cerevisiae105. To simulate different abundance levels, the FEY_15 nanopore reads were diluted with increasing numbers of Zymo metagenome reads at approximate ratios of 1:1, 1:10, 1:100, and 1:1000 based on number of base pairs. All of the FEY_15 and Zymo metagenome Illumina reads were combined together at an approximate ratio of 1:20 (Fig. 6a). These read sets were then used for Prymetime assembly. In each read set, the integration and plasmid of FEY_15 were completely resolved (Fig. 6b). This shows that synthetic biology parts, and their context, can be resolved in mixed samples by Prymetime.
This work develops an integrated workflow for WGS of engineered yeasts which may be extensible to all eukaryotes with a mixture of linear and circular sequences. The workflow consists of gentle gDNA isolation, tagmentation, long- and short-read NGS, accurate de novo assembly of both linear and circular elements, and annotation of genetic engineering parts and genome features. Using this, diverse engineering signatures can be resolved in complete, contiguous sequences even with multiple similar plasmids in one strain. The resulting whole genome quality is comparable to high-quality reference assemblies, therefore, it is possible to generate accurate genome assemblies both before and after engineering. This permits verification of genetic engineering in yeasts with WGS to validate strain engineering. Further, the workflow performs well using metagenomic data, permitting detection of yeast engineering in mixed samples.
This work demonstrates the challenges in making effective WGS-based workflows. Interestingly, we found that only the Flye assembly algorithm supported accurate resolution of genetic engineering in complete, contiguous sequences. We observed that sequence omission commonly occurred with assemblers built around OLC algorithms, which struggle to reproduce the expected representation and resolution of repeats68,69,106. Furthermore, we observed that short-read and hybrid assemblers commonly produced fragmented sequences. Thus, Flye, as the only long-read DBG assembler, was consistently the best at resolving genetic engineering signatures. These observations highlight the difficulty of applying otherwise effective genome assembly software to engineered yeasts, which have highly identical genetic engineering signatures and repetitive genome features. Furthermore, all assemblers collapsed repetitive genome features and struggled to resolve telomeres. This limits the ability of the tool to detect variations in rDNA, SNPs, and rare variants. Based on our results, assemblers aiming to improve these areas should be benchmarked against the overall performance of Flye.
To date, WGS has rarely been used in strain engineering cycles due to the barriers of cost, time, and required bioinformatics expertise. The WGS workflow we developed with the inexpensive ONT MinION and Illumina iSeq 100 platforms and the integrated, dockerized Prymetime software package overcomes these barriers. With Prymetime, we were able to achieve high-quality genomes at relatively low read depth, finding that 40X for both long and short reads was sufficient for high accuracy, completeness, and contiguity of genetic engineering sequences, and quality whole genomes. With 40X read depth, up to 30 S. cerevisiae genomes can be sequenced on one MinION flow cell and up to 4 genomes can be sequenced on one Illumina iSeq flow cell. This is because approximately 0.5 Gb is needed for 40X read depth of the 13.4 Mb S. cerevisiae genome (factoring in collapsed rDNA repeats107) and our typical yield is approximately 15 Gb from the MinION and 2.4 Gb from the iSeq 100. Not accounting for labor, this level of multiplexing would cost around $200 per genome. The entire workflow is fast – it takes under a week to start from a single colony and acquire a genome assembly, requiring only 15 h of hands-on time. Our workflow requires only a few coding steps – future users can simply load NGS reads and run the Prymetime script to detect and validate genetic engineering.
Strains and media
Parent strains for all engineered strains are shown in Supplementary Table S1. All yeast strains were grown in yeast extract-peptone-dextrose (YPD) or synthetic complete (SC)+glucose media. YPD consisted of 30 g/L YEP (10 g/L yeast extract + 20 g/L peptone, Sunrise Science, 1877-1KG) and 20 g/L glucose (Alfa Aesar, A16828). SC + glucose media consisted of 6.71 g/L of YNB+Nitrogen (1.71 g/L yeast nitrogen base + 5 g/L ammonium sulfate, Sunrise Science, 1501-250), 20 g/L glucose, and a formulation of complete synthetic media (CSM). CSM formulations were (1) CSM-Leu: 0.65 g/L CSM-His-Leu-Ura (Sunrise Science, 1015-010) + 0.02 g/L Histidine (Sunrise Science, 1978-010) + 0.02 g/L Uracil (Sunrise Science, 1906-010) and (2) CSM-Trp-Ura: 0.62 g/L CSM-Leu-Trp-Ura (Sunrise Science, 1017-010) + 0.1 g/L Leucine (Sunrise Science, 1980-010). For the K. phaffii transformation, 2xYPD was prepared with 75 g/L YEP plus 20 g/L glucose, and YPDS plates were prepared by supplementing YPD agar with 1M sorbitol (Acros, 132730010). If appropriate, antibiotic selection was performed with nourseothricin at 0.1 g/L for S. cerevisiae and K. phaffii (Jena Bioscience, AB-101-10ML), geneticin at 0.2 g/L for S. cerevisiae and 0.3 g/L for K. phaffii (Life Technologies Gibco, 10131-035), and/or hygromycin B at 300 mg/L for S. cerevisiae (Thermo Fisher, 10687010). Routine growth conditions were as follows: inoculation in 5 mL media in a 14 mL Falcon tube (Corning, 352059), incubation at 30∘, and shaking at 220 rpm or agitation on a rotating drum.
Chemically competent E. coli DH5α (NEB, C2987H) was used as a cloning strain and grown in 25 g/L LB Miller broth (10 g/L tryptone + 5 g/L yeast extract + 10 g/L sodium chloride, Fisher Scientific, BP1426-2). Antibiotic selection was performed with 100 mg/L ampicillin (Alfa Aesar, J63807), 25 mg/L chloramphenicol (Alfa Aesar, B20841), or 50 mg/L kanamycin (Alfa Aesar, J61272). Solid media was supplemented with 20 g/L agar (Sunrise Science, 1910-1KG).
Polymerase chain reaction (PCR)
PCR reactions were performed using the Q5 2X Master Mix (NEB, M0492L). Primers for PCR were designed with Benchling (https://benchling.com/, quality controlled with the New England Biolabs Tm Calculator (https://tmcalculator.neb.com/), and ordered from IDT (Integrated DNA Technologies, Inc., Skokie, Illinois). Reactions were performed in a total volume of 50 μL, with 25 μL of the Q5 Master Mix, 2.5 μL of both the forward and reverse primers (at 10 μM), X μL of template DNA (1 ng plasmid DNA, 100 ng genomic DNA), and 20-X μL of nuclease free water (VWR 02-0201-0500). PCR settings were determined based on instructions from NEB:
98C for 30 sec
30 PCR cycles:
98C for 10 sec
annealing temp. for 15 sec
72C for 20 sec per kbp
72C for 2 min
Modular cloning with TypeIIS restriction enzymes was used to assemble genetic designs. Modular cloning uses a hierarchical assembly process to make parts, transcription units, and pathways. TypeIIS cloning reactions were based on the TypeIIS enzymes BbsI (10 U/μL, Thermo Scientific, ER1011) or BsaI (10 U/μL, NEB, R0535). DNA parts were diluted to 20 fmol/μL, with 1 μL of each part used in the reaction (2 parts for L0 assembly, 4 parts for L1 assembly). 7.9 - N parts (2 or 4) μL of nuclease free water was added to a PCR tube (USA Scientific, 1402-4700). Next, 1 μL of 10X Ligase Buffer and 0.4 μL of 20 U/μL T4 DNA ligase (Promega, M1794) was added to the tube. Finally, 1 1 μL of either the BbsI (L0 assembly) or BsaI (L1 assembly) enzymes was added to the reaction, yielding a total reaction of 10.3 μL. The reaction was then run on a thermocycler with the following conditions: 37 ∘C for 5 h, 50 ∘C for 15 min, 80 ∘C for 20 min, and a hold at 10 ∘C.
Gibson assembly reactions followed instructions from the NEBuilder HiFi DNA Assembly Master Mix (NEB, E2621S). Briefly, PCR was used to amplify fragments with overlapping sequences (20–30 bp overlaps). When appropriate, the DpnI enzyme was used to digest template plasmid (NEB, R0176S) per instructions. The fragments were diluted to 0.2 pmols for 2–3 fragments or 0.5 pmols for 4 or more fragments in nuclease-free water, and transferred to a PCR tube. 10 μL of the HiFi master mix was added along with nuclease free water to reach a total reaction volume of 20 μL. The reaction was then run on a thermocycler at 50 ∘C for 60 min, followed by a hold at 10 ∘C.
S. cerevisiae transformations were done based on the lithium acetate method108. S. cerevisiae cells from a glycerol stock were inoculated in 5 mL of YPD in a 14 mL Falcon tube and shaken overnight on a rotating drum at 30 ∘C. In the morning, these cells were used to inoculate 5 mL of fresh YPD to a density of OD = 0.25. The cells were incubated at 30 ∘C on a rotating drum until OD = 1.0 (approximately 4 h). The cells were then pelleted at 500 × g for 5 min, washed with 2.5 mL of sterile water, and centrifuged again at 500 × g for 5 min. The cells were resuspended in 100 μL of 100 mM lithium acetate (TCI, L0191) and transferred to a 1.5 mL microcentrifuge tube (USA Scientific, 1615-5500). The cells were pelleted at 500 × g for 30 s, resuspended to a total volume of 50 μL in about 40 μL of 100 mM lithium acetate, and then flicked to mix. The following were then added to the cell mixture: 240 μL PEG 3350 (VWR, 0955), 36 μL 1.0 M lithium acetate, 5 μL boiled salmon sperm DNA (Invitrogen AM9680, 10 μg/μL), and 50 μL transforming DNA. Between each addition to the cell mixture, the microcentrifuge tube was flicked to completely mix. The salmon sperm DNA was prepared by boiling for 5 min on a thermocycler at 100 ∘C. The tube was then incubated at 30 ∘C for 30 min, followed by the addition of 35 μL of dimethyl sulfoxide (DMSO, Sigma, D8418). The heat shock step followed at 42 ∘C for 15 min. For auxotrophic selection, the cells were plated onto CSM knockout agarose plates. For antibiotic selection, the cells were pelleted at 500 × g for 30 s followed by removal of the transformation mixture. 1 mL of YPD was used to gently resuspend the cell pellet and transferred to 4 mL of fresh YPD in a Falcon tube. The cells were allowed to incubate overnight at 30 ∘C, and then plated onto YPD agarose plates with the appropriate antibiotic. For both auxotrophic and antibiotic selections, the plates were incubated at 30 ∘C until transformants appeared (typically 2–4 days).
Transformation of K. phaffi was performed by electroporation28. A 10 mL preculture in a 100 mL flask was inoculated from a glycerol stock and grown overnight at 30 ∘C with shaking at 200 rpm. The next morning, 50 μL of preculture was tranferred into 100 mL fresh YPD in a 250 mL flask, and this culture was incubated overnight again to OD600 = 1.3–1.5. This culture was harvested into three 50 mL conical tubes and pelleted at 4 ∘C, 1,500 × g for 5 min. The media was decanted and the pellet was resuspended by tapping firmly. The three pellets were resuspended in ice-cold sterile water and combined into one tube to a total of 40 mL. The cells were pelleted again, decanted, and resuspended in 20 mL ice-cold water. The cells were pelleted again and resuspended in 20 mL ice-cold 1 M sorbitol. The cells were pelleted again, the sorbitol was decanted, and the pellet was loosened by tapping firmly. 500 μL of ice-cold sorbitol was added to the pellet and mixed by flicking. These electrocompetent cells were stored on ice. Electroporation cuvettes (2 mm gap, Molecular BioProducts, 5520) were stored on ice during the centrifugation steps, and DNA was added to the bottom (5–10 μg for plasmid DNA, 5–20 μg linearized DNA for integration, or 10 μg circular transfer vector plus 10 μg recombinase expression vector for recombinase-based transformations). 80 μL of competent cells were added to the DNA-containing electroporation cuvettes and incubated on ice for 5 min. Cells were electroporated at 1500 V, then transferred into a round-bottom Falcon tube containing 1 mL 2xYPD at room temperature. Cells were recovered overnight at 30 ∘C with shaking at 200 rpm and 100–200 μL was plated onto YPD antibiotic plates. Plates were incubated at 30 ∘C until colonies appeared (2–4 days).
Transformation of Y. lipolytica was performed by chemical transformation109. A 10 mL preculture in a 250 mL flask was inoculated from a glycerol stock and incubated at 30 ∘C with shaking at 200 rpm overnight. The next day, 25 mL of fresh YPD was inoculated from the preculture to OD6O00 = 0.5, and incubated for at 30 ∘C with shaking. After 3 h, 250 μL of 5 M hydroxyurea (Sigma H8627) was added to the culture, and incubation was continued for another 2 h. The cells were then transferred to a 50 mL conical tube (Greiner bio-one, 227261), centrifuged at 1500 × g for 5 min, and washed twice with 10 mL sterile deionized water. The pellet was resuspended to OD600 = 50 in 0.1M lithium acetate. For each transformant, 100 μL was transferred to a 1.5 mL microcentrifuge tube, which was centrifuged at 1500 × g for 5 min. The supernatant was removed and the following were added: 90 μL of 50% PEG-3350, 5 μL of 2 M ditriothreitol (G Bioscience, 277D-E), 5 μL of 2 M lithium acetate, and 2.5 μL of sheared, boiled salmon sperm DNA (10 μg per μL). This cocktail was mixed well with the cells by vortexing, then 5–10 μg of plasmid DNA in less than 40 μL was added and mixed by flicking. The cell and DNA mixture was then heat shocked at 39 ∘C for 1 h. The entire transformation mixture was plated onto SC media without leucine and incubated at 30 ∘C until colonies appeared (4 days).
Parts and plasmids
All genetic parts used in this study and their sources are detailed in Supplementary Table S10. Parts made for this study were synthesized by Integrated DNA Technologies (IDT). Design included codon optimization using IDT’s proprietary algorithm and elimination of BsaI and BbsI restriction sites.
This study used cloning plasmids, integrating plasmids, and shuttle vectors. Plasmids built for this study are depicted in Supplementary Fig. S3. In modular cloning, plasmids that maintain transcriptional parts are referred to as Level 0 (L0) plasmids and plasmids maintaining transcription units are referred to as Level 1 (L1) plasmids. The L0 plasmids used in this study – pJHC07AB (Supplementary Fig. S3a), pJHC07BC (Supplementary Fig. S3b), pJHC07CD (Supplementary Fig. S3c) – are derived from pEMY07AB, pEMY07BC, and pEMY07CD51. These were constructed using Gibson assembly (NEB, E2611S) to replace the lacZ selection gene with the ccdb selection gene110. Plasmid pJHC07AB maintains promoters, pJHC07BC maintains ORFs (genes), and pJHC07CD maintains terminators. Integrating L1 plasmids built for this study included pJHC15HR1 (Supplementary Fig. S3d), pJHC15HR2 (Supplementary Fig. S3e), pJHC15HR3 (Supplementary Fig. S3f), pJHC15HR4 (Supplementary Fig. S3g), pJHC15HR5 (Supplementary Fig. S3h), and pJHC15HR6 (Supplementary Fig. S3i). These were constructed using Gibson assembly, and included two connector sequences, the ccdB selection gene, the chlR cassette, and ColE1 replicon. The connector sequences are sequentially homologous 60bp spacers, such that the 3′ spacer of pJHC15HR1 is homologous to the 5′ spacer of pJHC15HR2 and so forth. Once a transcription unit was assembled into these plasmids, PCR was used amplify the transcription unit fragment and the flanking connectors. These fragments were integrated into the S. cerevisiae genome using the native homologous recombination pathway, similar to DNA assembler29. We targeted two S. cerevisiae loci – ChrXV and HO (definitions and ref to supplement). The shuttle vector pCY112 built for this study is depicted in Supplementary Fig. S3j. It was constructed using Gibson assembly, and contains the ccdB selection gene, ColE1 replicon, chlR cassete, the low copy yeast replicon CEN6/ARSH4, and the Klleu2 auxotrophic cassette. Parts and plasmids specific to each strain are described in the next section.
Yeast strain design and construction
The parent strain was S. cerevisiae S288C hap1:HAP1111. The design was a metabolic pathway for synthesis of valine-derived chemicals (Supplementary Fig. S4a). The sequences for acetolactate synthase(ahas1), ketol-acid reductoisomerase (ilv6), and dihydroxy-acid dehydratase (ilvD1) were derived from Penicillium chrysogenum112. The sequence for aldehyde decarbonylase (ado) was derived from Prochlorococcus marinus113. The sequence for alpha-ketoisovalerate decarboxylase (kivD) was derived from Lactococcus lactis114. These CDSs were cloned into pJHC07BC using TypeIIS assembly. Transcription units were then built by combining L0 promoter, CDS, and terminator plasmids into a L1 integrating plasmid. The resulting transcription unit plasmids were pJHC15HR1-Ptef1-ahas1-Ttip1, pJHC15HR2-Psmtef1-ilv6-Tprm9, pJHC15HR3-Phta1-ilvD1-Tyhi9, pJHC15HR4-Pagtef1-nat-Tagtef1, pJHC15HR5-Psptdh3-ado-Trpl41b, and pJHC15HR6-Ptdh3-kivD-Trpl15a. Each level 1 vector was linearized by PCR and transformed into S.cerevisiae strain S228c, along with homology arms for the ChrXV integration locus (with the 5′ arm containing the spacer homologous to the pJHC15HR1 5′ spacer and 3′ homology arm containing the spacer homologous to the pJHC15HR6 3′ spacer). The primers used to amplify the homology arms from genomic DNA are included in Supplementary Table S10. The linearized fragments then assembled by yeast assembly. Transformants were selected on YPD with nourseothricin and verified by PCR.
The parent strain was S. cerevisiae CEN.PK113-7D115. The design was a metabolic pathway for the synthesis of β-carotene (Supplementary Fig. S4b). The sequences for geranylgeranyl diphosphate synthase (crtE), bifunctional lycopene cyclase/phytoene synthase (crtYB), and phytoene desaturase (crtI) were sourced from a previous study87. These coding sequences were synthesized, cloned into L0 pEMY07BC vectors with a BbsI type IIs reaction, assembled into level 1 transcription units (Psbtdh3-crtE-Trpl41b, Psptdh3-crtYB-Tyol036w, Phta2-hyg-Tagtef1, and Psmtef1-crtI-Trpl15a) with BsaI type IIs reactions, and integrated into the ChrXV locus as described above; however, the construct was integrated into strain CEN.PK113-7D and selected on YPD with hygromycin B. Plasmids pAG700 and pAG22-2 are dCas9 and gRNA expression plasmids, respectively, and were provided by Amar Ghodasara. Each plasmid was sequentially transformed into the above-described crt pathway integration strain with selection on YPD with hygromycin B, geneticin, and nourseothricin to yield FEY_2.
The parent strain was CEN.PK113-7D. The design was a fluorescent protein integrated into a genomic locus with an antibiotic selection marker (Supplementary Fig. S4c). The sequence for the fluorescent protein encoding gene yEmCitrine was sourced from a previous study92 and cloned into L0 vector pEMY07BC with a BbsI type IIs reaction. Level 1 transcription units Pact1-yEmCitrine-Tadh1 and Pagtef1-Nat-Tagtef1 were assembled into pJHC15HR1 and pJHC15HR2 with BsaI type IIs reactions and were integrated into the ChrXV locus as described above.
The parent strain was CEN.PK113-7D. The design was an inducible deactivated Cas9 expression cassette integrated into a chromosomal locus along with a high-copy replicating vector containing the guide RNA expression cassette (Supplementary Fig. S4d).The deactivated Cas9 (dCas9Mx1) sequence was sourced from a previous study35 and cloned into pEMY07BC. Transcription units Pgal10-dCas9Mx1-Tspo1 and Psptef1-nat-Ttip1 were assembled in pJHC15HR1 and pJHC15HR2 with BsaI type IIs reactions and integrated into the HO locus (HO locus homology arm primers included in Supplementary Table S10). Yeast shuttle vector pY128 containing the insert Psnr52-gRNAscr-TtracrSUP4 was subsequently transformed into the integration strain to yield FEY_15. The pY128 vector was sourced from a previous study51.
The parent strain was S. cerevisiae strain W30311. The design was a Cas9 expression cassette on a low copy number plasmid and a guide RNA expression cassette on a high copy number plasmid (Supplementary Fig. S4e). Plasmids p414-Tef1p-Cas9-Cyc1t and p426-Snr52p-gRNA.CAN1.Y-Sup4t30 were purchased from Addgene (43802 and 43803).
The parent strain was S288C hap1:HAP1. The design was a Cpf1 expression strain on a low copy number plasmid (Supplementary Fig. S4f). Plasmid pCSN06738 was purchased from Addgene (101748).
The parent strain was S288C hap1:HAP1. The design was a Cpf1 programming crRNA expression strain on a high copy number plasmid (Supplementary Fig. S4g). Plasmid pUDE72237 was purchased from Addgene (103022).
The parent strain was S288C hap1:HAP1. The design was a Cre expression strain on a low copy number plasmid (Supplementary Fig. S4h). Plasmid pSH6633 was purchased from Euroscarf (P30672).
The parent strain was S288C hap1:HAP1. The design was a single enzyme expression strain on a high copy number plasmid (Supplementary Fig. S4i). The sequence for prespatane sesquiterpene synthase (pst) was derived from Laurencia pacifica88. This coding sequence was synthesized, cloned into level 0 vector pEMY07BC with a BbsI type IIS reaction, and cloned with Ppgk1 and Ttdh1 by BsaI type IIS reactions into the level 1 shuttle vector pY128. Shuttle vector pY128 contains the endogenous yeast 2μ plasmid origin of replication.
The parent strain was S288C hap1:HAP1. The design was a three enzyme pathway integrated into a chromosomal locus with an antibiotic selection marker (Supplementary Fig. S4j). The sequence for bifunctional diterpene synthase (mdst) was derived from Selaginella moellendorffii116. The sequence for bifunctional ferruginol, 11-hydroxyferruginol synthase (hfst) was derived from Salvia pomifera117. The sequence for 11-hydroxyferruginol C20-oxidase (cast) was derived from Salvia rosmarinus89. These coding sequences were synthesized and cloned into level 0 vector pEMY07BC with BbsI. Transcription units Psktef1-mdst-Tecm10, Psptef1-nat-Ttip1, Psmtdh3-hfst-Ttdh3, and Psmtef1-cast-Teno1 were assembled into pJHC15HR1-4 with BsaI, linearized by PCR, and integrated into the HO locus as described above.
The parent strain was S288C hap1:HAP1. The design was a two enzyme pathway integrated into a chromosomal locus with an antibiotic selection marker (Supplementary Fig. S4k). The sequence for dimethylallylcistransferase (nppst) was derived from Solanum lycopersicum118. The sequence for limonene synthase was derived from Citrus limon119. These coding sequences were synthesized and cloned into level 0 vector pEMY07BC with BbsI. Transcription units Psbtef1-nppst-Tecm10, Psptef1-nat-Ttip1, and Psktdh3-lst-Ttdh1 were assembled into pJHC15HR1-3, linearized by PCR, and integrated into the HO locus as described above.
The parent strain was S. cerevisiae BY474213. The design was a monocistronic dual fluorescent protein construct integrated into a chromosomal location as well as an empty yeast shuttle vector with a low copy number origin and auxotrophic complementation marker (Supplementary Fig. S4l). The yEGFP-2A-mRuby sequence was designed by combining the yEGFP and mRuby sequences from Sheff et al.92 and Lee et al.93, respectively, with a self-cleaving 2A sequence94. This coding sequence was cloned into level 0 vector pEMY07BC with BbsI. Transcription units Psptef1-yEGFP-2A-mRuby-Trps9a and Psptef1-nat-Ttip1 were assembled into pJHC15HR1-2 with BsaI, linearized by PCR, and integrated into the HO locus of BY4742 as described above. The lacZα insert of pEMY11251 was substituted with a ccdB insert to form pCY112, which was then transformed into the EGFP-2A-mRuby integrated strain above. The plasmid pCY112 contains the CEN6/ARSH4 yeast plasmid origin of replication.
The parent strain was S. cerevisiae BY474113. The design was a low copy number yeast shuttle vector expressing a fluorescent protein (Supplementary Fig. S4m). Plasmid pKK1112(Prev1-Venus-Teno2//LEU2//CEN6//KanR-ColE1) was generated using parts from the MoClo Yeast Toolkit27. The following level 0 parts were combined with BsaI into an eight-part level 1 shuttle vector: pYTK084, pYTK002, pYTK027, pYTK033, pYTK055, pYTK067, pYTK075, and pYTK081.
The S. cerevisiae strain BY4743120 was used without modification.
The parent strain was Y.lipolytica strain Po1f16. The design was a plasmid expressing Cas9 (Supplementary Fig. S4n). Plasmid pCRISPRyl39 was purchased from Addgene (103022).
The parent strain was K.phaffii strain CBS 7435 (ATCC 76273). The design was a fluorescent protein expression cassette integrated into a genomic locus by site-specific recombination (Supplementary Fig. S4o). The strain containing an attP site for BxbI-mediated recombination was created by transforming plasmid PP74 linearized by AccI (NEB, R0161S) into the parent strain as described by Perez-Pinera28. An integrating vector pKK2147(Pgap-aMFnoEAEA-RFPsec-Taox1) was constructed by combining pYTK084, pYTK002, pYTK067, and pYTK07827 with pPTK002, pPTK006, pPTK018, pPTK019, and pPTK020 in a 9-part BsaI type IIs reaction as described by Obst121. This integration vector was co-transformed with BxBI expression plasmid PP43 into the attP-containing strain and selected on YPD plates with nourseothricin and G418 to yield FEY_75.
High-molecular weight genomic DNA isolation
Genomic DNA was isolated using Promega’s Genomic DNA Isolation Kit (Promega, A1120). A modified version of Promega’s protocol for yeast gDNA isolation was used to limit shearing of DNA, with added insight from Josh Quick’s Ultra-long read sequencing protocol122. No vortexing and limited pipetting/mixing steps were used to maximize Nanopore read lengths. 5 mL of cells were grown overnight (or until saturation) at 30. The cells were pelleted at 500 × g for 5 min, and resuspended in 1.5 mL of 50 mM EDTA (Millipore, 324506) and 37.5 μL of 5 U/μL zymolyase (Zymo, E1004). The samples were incubated at 37 °C for 1 h to allow the Zymolyase to digest the cell wall. The cells were pelleted at 500 × g for 5 min, re-suspended in 1.5 mL of the Nuclei Lysis Solution (mix by inversion, flicking), and incubated at room temperature for 30 min. 7.5 μL of RNAse A Solution was then added and incubated for 15 min at 37 °C. Once cooled to room temperature, 500 μL of the protein precipitation solution was added (invert to mix). The samples were put on ice for 5 min, and subsequently centrifuged for 10 min at 3000 × g. 700 μL of the supernatant was added to a fresh microcentrifuge tube with 700 μL of isopropanol (Sigma, I9516). The microcentrifuge tubes were gently mixed by inversion and centrifuged at 4000 × g for 1 min. The DNA pellet was washed with 70% ethanol (Sigma, E7023) and centrifuged at 4000 × g for 1 min. The ethanol was carefully pipetted off the DNA pellet, and the tube cap was left open at room temperature for 20 min to allow residual ethanol to evaporate. 50 μL of 10 mM Tris-HCl (Alfa Aesar, J67233) and 0.02% Triton X-100 (Sigma-Aldrich, X100-500ML) was added to resuspend the DNA pellet and incubated overnight at 4 °C. DNA quality was evaluated using a Nanodrop, and the concentration was calculated using a Qubit.
Nanopore DNA library preparation and MinION loading
The Rapid Barcoding Kit was used to tagment the DNA libraries for sequencing (ONT, SQK-RBK004). Up to four genomes were multiplexed on each MinION flow cell. Library preparation closely followed the protocol provided by ONT. Briefly, 400 ng of template DNA for each isolate was diluted to 7.5 μL, mixed with 2.5 μL of the Fragmentation Mix, and then incubated at 30 ∘C for 1 min and 80 ∘C for 1 min on a thermal cycler. The barcoded samples were then pooled together and concentrated using AMPure XP beads in 10 μL of 10 mM Tris-HCl, 50 mM NaCl. The pooled sample was next mixed with 1 μL of RAP for 5 min at room temperature, and stored on ice until ready to load. R9.4 MinION Flow Cells (ONT, FLO-MIN106) were used for all sequencing runs. The flow cells were first primed per ONT’s instructions. The 11 μL of prepped DNA was mixed with 4.5 μL of nuclease-free water, 34 uL of SQB, and 25.5 μL of LLB and loaded onto the MinION flow cell. Sequencing runs were executed using ONT’s MinKNOW software (v8.3.1) with the default settings.
Nanopore fast5 files were basecalled using Guppy v2.3.5 (Oxford Nanopore base caller). The subsequent fastq files were demultiplexed using the EPI2ME interface (Metrichor, Oxford, UK). Illumina reads were demultiplexed using the native software on the iSeq machine. Random subsets of Illumina and Nanopore reads at a specific genome coverage were generated using a custom python script (https://github.com/aseetharam/common_scripts/blob/master/sample_fastq.py).
For the metagenome experiment, nanopore and illumina reads from FEY_15 and the zymo mock metagenome were combined into the same nanopore and Illumina fastq file. FEY_15 Nanopore reads at 10X genome coverage were used for each read dilution experiment. The number of zymo mock metagenome nanopore reads was based off the estimated number of base pairs in the FEY_15 read library. The genome size of S. cerevisiae is 12.1 Mb, so 10X genome coverage is 121 Mb. Therefore, the nanopore read library sizes of the zymo mock metagenome were 121 Mb (1:1), 1210 Mb (1:10), 12100 Mb (1:100), and 121000 Mb (1:1000). All of the Illumina reads from FEY_15 and the zymo mock metagenome were simply combined into one file and used for each of the four dilution experiments.
Illumina DNA library preparation and iSeq 100 loading
The Nextera DNA Flex Library Prep Kit (Illumina, 20018704) along with the Nextera DNA CD Indexes (Illumina, 20018707) were used to tagment the DNA libraries for sequencing. Library preparation closely followed the instructions provided by Illumina, and up to four genomes were multiplexed on one Illumina sequencing cartridge. Briefly, tagmentation was first performed with 500 ng of genomic DNA in 30 μL of nuclease-free water. The reaction was stopped by adding 10 μL of both the BLT and TB1 reagents and incubating at 55∘C for 15 min on a thermal cycler. Index adapters for each sample along with EPM were then added to barcode and amplify the genomic DNA. The DNA libraries were amplified using the following PCR program:
68C for 3 min
98C for 3 min
5 PCR cycles:
98C for 45 sec
62C for 30 sec
68C for 2 min
68C for 1 min
The DNA libraries were cleaned using subsequent steps with the SPM reagent and 80% ethanol, and concentrated in 32 μL of the RSB reagent. Assuming four genomes were multiplexed on one flow cell, 25 pM of each DNA library were pooled together in 100 μL of the RSB reagent and stored on ice until ready to load. The pooled libraries were loaded onto the sequencing cartridges according to Illumina’s instructions. The Local Run Manager on the iSeq 100 machine was used to initiate sequencing runs. A GENERATEFASTQ run was started, and run with the parameters Read Type: Paired End, Read Lengths: 151, and Index Reads: 2.
Nanopore de novo genome assembly
For the MiniASM68 assembly, reads were first mapped using minimap2 (v2.17-r941)61 with the parameters "-x ava-ont -t8”. MiniASM (v0.3) was then subsequently run with the default parameters. Canu69 (v1.8) was run with the parameters "minReadLength=2500 mhapSensitivity=high corMhapSenstivity=high corOutCoverage=500”. SMARTdenovo70 (v1.0) was run using the parameters "-c 1 -k 14 -J 2500 -e zmo”. Flye71 (v2.4) was run with the parameters "–meta –plasmids". ABySS64 (v 2.1.5) was run with the abyss-pe option and the parameter "k=96". Edena63 (v3.131028) was run with the default parameters. Velvet65 (v1.2.10) was run with a hashlength of 21 bp. MaSuRCA (v3.3.4) was run with the parameter "JF_SIZE = 242000000 FLYE_ASSEMBLY=1". SPAdes (v3.13.1) was run with the parameters "–sc –nanopore –pe < # > -1 –pe < # > -2".
Nanopore and Illumina read polishing
The de novo Nanopore genome assemblies were first polished with Nanopore reads using Medaka (v0.4) with the default parameters. The assembly was then polished with Illumina reads, first with Racon (v1.3.1) followed by Pilon (v1.22). For Racon, the Illumina reads were first mapped to an assembly using minimap2 with the parameter "-ax sr”. Racon78 was then run using the default parameters. For Pilon, assemblies were first indexed using bwa (v0.7.17-r1188)123. Illumina reads were then mapped to the assembly using bwa with the parameter "mem -t 14”. Pilon79 was then run using the parameter "-Xmx160G”.
Prymetime genome assembly workflow
Visualization of the full Prymetime workflow is shown in Supplementary Fig. S20. First, Flye (v2.4) was run with the parameters "–meta –plasmids" on a Nanopore fastq file to generate the initial genome assembly. Contigs in the resulting assembly file were separated into circular or linear contig files. This was accomplished using a custom python script and the assembly_info.txt file resulting from Flye. The linear contigs were polished first with Medaka (Nanopore reads), followed by Racon and Pilon (Illumina reads). Medaka was run with the default parameters. In preparation for Racon polishing, the Illumina reads were mapped using minimap2 with the parameter "-ax sr". Racon was then run with the default parameters. For Pilon preparation, the assembly was first indexed with bwa, followed by mapping with bwa and the parameter "mem -t 14". Pilon was then run with the parameter "-Xmx160G". To find potential circular contigs that Flye may have missed, a custom python script was used on the polished linear contigs file. The script used the Mummer option nucmer (v3.1)124 with the parameters "maxmatch = True, simplify = False, mincluster = 2000, min_id = 99, min_length = 2000, coords_header = True" on contigs that were less than 50,000 bp to identify repetitive contigs. The repetitive contigs were extracted and combined with the circular contigs from the initial Flye assembly, and sent to be re-assembled with Unicycler (v0.4.8). In order to do this, the contigs were first separated into separate fasta files using awk (v4.0.2). Nanopore and Illumina reads were then mapped to each individual contig, with matches extracted into fastq files. The Nanopore reads were mapped using minimap2 with the parameters "-ax map-ont" followed by extraction of hits with samtools (v1.9) and the parameters "fastq -n -F 4 -". Each paired-end Illumina file was mapped using minimap2 with the parameter "-ax sr" followed by extraction of hits with samtools and the parameters "fastq -n -F 4 -". The resulting two Illumina files were paired using fastq_pair (v1.0) with the default parameters125. Unicycler was then run with the mapped and paired Illumina files along with the mapped Nanopore file with the default parameters82. The re-assembled circular and repetitive contigs resulting from Unicycler were combined with the polished linear contigs, yielding the final assembly.
Prymetime annotation and visualization of engineering and genome features
Non-native engineering signatures were detected in the genome assemblies using BLASTN (v2.5.0) with the parameters "-perc_identity 98 -qcov_hsp_perc 98". The query for this BLASTN search was a curated list of all non-native engineering signatures used to engineer the yeast strains in this study, and are included in the Prymetime package. The genome features telomeres, centromeres, and mitochrondrion were detected using BLASTN with the parameters "-max_target_seqs 1 -max_hsps 1". The genome feature sequences were downloaded from the Saccharomyces Genome Database100, and are included in the Prymetime package. The genome plotter chromoMap (v0.2)101 was run with the parameters "data_based_color_map = T, data_type = "categorical" to show the engineering signatures and genome elements hits from the BLASTN search in the context of the entire genome assembly. The genome alignment and visualization software AliTV (v1.0.6) was run with the default parameters102.
Genome assessment tools
QUAST126 (v5.0.0) was run with the default parameters, yielding the metrics number of contigs, maximum contig length, and N50. For accuracy-related metrics, the nucmer command was run as part of the MUMmer package124. The command "dnadiff -d" was used on the resulting delta file to find the average identity to the reference and the number of SNPs. Genome assemblies were evaluated for genome completeness using BUSCO (v4.0.6)95 with the saccharomycetales_odb9 datasets, as well as a BLASTN40 search of ORFs from S. cerevisiae S288C. Engineered signatures were searched for in-genome assemblies using BLASTN with the expect threshold set at 0.0001.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Illumina and nanopore raw reads from all engineered yeast strains have been deposited to DDBJ/ENA/GenBank under the BioProject PRJNA650312. Illumina and nanopore raw reads from the non-engineered yeast strains have been deposited to DDBJ/ENA/GenBank under the BioProject PRJNA694170. All yeast genome assemblies from this study (engineered and non-engineered) are available in https://github.com/emyounglab/prymetime_genomes.
Prymetime can be accessed as a Docker image on GitHub at https://github.com/emyounglab/prymetime. The Prymetime code has been published on Zenodo, https://doi.org/10.5281/zenodo.4440108.
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The authors thank James Kingsley at WPI for his help implementing Prymetime on WPI’s server. This research is based upon work supported in part by the Office of the Director of National Intelligence (ODNI), Intelligence Advanced Research Projects Activity (IARPA) under Finding Engineering Linked Indicators (FELIX) program contract #N66001-18-C-4507. The views and conclusions contained herein are those of the authors and should not be interpreted as necessarily representing the official policies, either expressed or implied, of ODNI, IARPA, or the U.S. Government. The U.S. Government is authorized to reproduce and distribute reprints for governmental purposes notwithstanding any copyright annotation therein. This work is also supported by Worcester Polytechnic Institute startup funds.
The authors declare no competing interests.
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Collins, J.H., Keating, K.W., Jones, T.R. et al. Engineered yeast genomes accurately assembled from pure and mixed samples. Nat Commun 12, 1485 (2021). https://doi.org/10.1038/s41467-021-21656-9
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