Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Novel bacterial clade reveals origin of form I Rubisco

Nature Plants volume 6, pages 1158–1166 (2020)Cite this article

Subjects

Abstract

Rubisco sustains the biosphere through the fixation of CO2 into biomass. In plants and cyanobacteria, form I Rubisco is structurally comprised of large and small subunits, whereas all other Rubisco forms lack small subunits. The rise of the form I complex through the innovation of small subunits represents a key, yet poorly understood, transition in Rubisco’s evolution. Through metagenomic analyses, we discovered a previously uncharacterized clade sister to form I Rubisco that evolved without small subunits. This clade diverged before the evolution of cyanobacteria and the origin of the small subunit; thus, it provides a unique reference point to advance our understanding of form I Rubisco evolution. Structural and kinetic data presented here reveal how a proto-form I Rubisco assembled and functioned without the structural stability imparted from small subunits. Our findings provide insight into a key evolutionary transition of the most abundant enzyme on Earth and the predominant entry point for nearly all global organic carbon.

This is a preview of subscription content, access via your institution

Relevant articles

Open Access articles citing this article.

Access options

Rent or buy this article

Get just this article for as long as you need it

$39.95

Learn more

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Metagenomics-enabled identification of a novel clade of form I Rubisco that lack small subunits.
Fig. 2: Comparison of P. breve Rubisco kinetic data to reported values of form I Rubisco.
Fig. 3: Solution-state characterization of form I' oligomerization reveals an octameric holoenzyme reminiscent of canonical form I Rubisco.
Fig. 4: Crystal structure of form I' Rubisco compared to cyanobacterial form I Rubisco.
Fig. 5: Structure of form I' Rubisco suggests that a tradeoff between stability and catalytic activity spurred the evolution of the small subunit.

Data availability

Form I' RbcL amino acid sequences are included as Supplementary Data 1. Sequences used to generate Fig. 1a were uploaded to figshare (https://doi.org/10.6084/m9.figshare.9980630) along with the associated phylogenetic tree. Representative MAG genbank scaffolds are included as Supplementary Data 2. Site-directed mutagenesis primers and synthesized candidate form I' rbcL genes are included as Supplementary Data 3. The structural coordinates of 2CABP-bound P. breve Rubisco have been deposited in the PDB under the accession ID 6URA. The crystal structure of Syn6301 Rubisco can be found on the PDB under the accession ID 1RBL. Publicly available databases used in this study include: PDB (https://www.rcsb.org/), pfam (https://pfam.xfam.org/), TIGRfams (www.tigrfams.jcvi.org) and KEGG database (https://www.genome.jp/).Two Chloroflexi genomes identified in this study are available at: https://ggkbase.berkeley.edu/Chloroflexi_Rubisco_PatrickShih/organisms.

References

  1. Nisbet, E. G. et al. The age of Rubisco: the evolution of oxygenic photosynthesis. Geobiology 5, 311–335 (2007).

    CAS  Google Scholar 

  2. Tabita, F. R. et al. Function, structure, and evolution of the RubisCO-like proteins and their RubisCO homologs. Microbiol. Mol. Biol. Rev. 71, 576–599 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Tabita, F. R., Satagopan, S., Hanson, T. E., Kreel, N. E. & Scott, S. S. Distinct form I, II, III, and IV Rubisco proteins from the three kingdoms of life provide clues about Rubisco evolution and structure/function relationships. J. Exp. Bot. 59, 1515–1524 (2007).

    Google Scholar 

  4. Andrews, T. J. Catalysis by cyanobacterial ribulose-bisphosphate carboxylase large subunits in the complete absence of small subunits. J. Biol. Chem. 263, 12213–12219 (1988).

    CAS  PubMed  Google Scholar 

  5. Morell, M. K., Wilkin, J. M., Kane, H. J. & Andrews, T. J. Side reactions catalyzed by ribulose-bisphosphate carboxylase in the presence and absence of small subunits. J. Biol. Chem. 272, 5445–5451 (1997).

    CAS  PubMed  Google Scholar 

  6. Spreitzer, R. J. Role of the small subunit in ribulose-1,5-bisphosphate carboxylase/oxygenase. Arch. Biochem. Biophys. 414, 141–149 (2003).

    CAS  PubMed  Google Scholar 

  7. Joshi, J., Mueller-Cajar, O., Tsai, Y.-C. C., Hartl, F. U. & Hayer-Hartl, M. Role of small subunit in mediating assembly of red-type form I rubisco. J. Biol. Chem. 290, 1066–1074 (2015).

    CAS  PubMed  Google Scholar 

  8. Liu, C. et al. Coupled chaperone action in folding and assembly of hexadecameric Rubisco. Nature 463, 197–202 (2010).

    CAS  PubMed  Google Scholar 

  9. Grabsztunowicz, M., Górski, Z., Luciński, R. & Jackowski, G. A reversible decrease in ribulose 1,5-bisphosphate carboxylase/oxygenase carboxylation activity caused by the aggregation of the enzyme’s large subunit is triggered in response to the exposure of moderate irradiance-grown plants to low irradiance. Physiol. Plant. 154, 591–608 (2015).

    CAS  PubMed  Google Scholar 

  10. Kusian, B. & Bowien, B. Organization and regulation of cbb CO2 assimilation genes in autotrophic bacteria. FEMS Microbiol. Rev. 21, 135–155 (1997).

    CAS  PubMed  Google Scholar 

  11. Tabita, F. R. Microbial ribulose 1,5-bisphosphate carboxylase/oxygenase: a different perspective. Photosynth. Res. 60, 1–28 (1999).

    CAS  Google Scholar 

  12. Whitney, S. M. & Andrews, T. J. The gene for the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) small subunit relocated to the plastid genome of tobacco directs the synthesis of small subunits that assemble into Rubisco. Plant Cell 13, 193–205 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Bryant, D. A. & Liu, Z. in Advances in Botanical Research (ed. Beatty, J. T.) 99–150 (Academic Press, 2013).

  14. Shih, P. M., Ward, L. M. & Fischer, W. W. Evolution of the 3-hydroxypropionate bicycle and recent transfer of anoxygenic photosynthesis into the Chloroflexi. Proc. Natl Acad. Sci. USA 114, 10749–10754 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Ward, L. M., Hemp, J., Shih, P. M., McGlynn, S. E. & Fischer, W. W. Evolution of phototrophy in the Chloroflexi phylum driven by horizontal gene transfer. Front. Microbiol. 9, 260 (2018).

    PubMed  PubMed Central  Google Scholar 

  16. Fischer, W. W., Hemp, J. & Johnson, J. E. Evolution of oxygenic photosynthesis. Annu. Rev. Earth Planet. Sci. 44, 647–683 (2016).

    CAS  Google Scholar 

  17. Roy, H. Rubisco assembly: a model system for studying the mechanism of chaperonin action. Plant Cell 1, 1035–1042 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Hayer-Hartl, M. From chaperonins to Rubisco assembly and metabolic repair. Protein Sci. 26, 2324–2333 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Aigner, H. et al. Plant RuBisCo assembly in E. coli with five chloroplast chaperones including BSD2. Science 358, 1272–1278 (2017).

    CAS  PubMed  Google Scholar 

  20. Wilson, R. H. & Hayer-Hartl, M. Complex chaperone dependence of Rubisco biogenesis. Biochemistry 57, 3210–3216 (2018).

    CAS  PubMed  Google Scholar 

  21. Saschenbrecker, S. et al. Structure and function of RbcX, an assembly chaperone for hexadecameric Rubisco. Cell 129, 1189–1200 (2007).

    CAS  PubMed  Google Scholar 

  22. Gunn, L. H., Valegård, K. & Andersson, I. A unique structural domain in Methanococcoides burtonii ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) acts as a small subunit mimic. J. Biol. Chem. 292, 6838–6850 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Goloubinoff, P., Christeller, J. T., Gatenby, A. A. & Lorimer, G. H. Reconstitution of active dimeric ribulose bisphosphate carboxylase from an unfolded state depends on two chaperonin proteins and Mg-ATP. Nature 342, 884–889 (1989).

    CAS  PubMed  Google Scholar 

  24. Parry, M. A. J., Keys, A. J. & Gutteridge, S. Variation in the specificity factor of C3 higher plant Rubiscos determined by the total consumption of ribulose-P2. J. Exp. Bot. 40, 317–320 (1989).

    CAS  Google Scholar 

  25. Tcherkez, G. G. B., Farquhar, G. D. & Andrews, T. J. Despite slow catalysis and confused substrate specificity, all ribulose bisphosphate carboxylases may be nearly perfectly optimized. Proc. Natl Acad. Sci. USA 103, 7246–7251 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  26. Flamholz, A. I. et al. Revisiting trade-offs between Rubisco kinetic parameters. Biochemistry 58, 3365–3376 (2019).

    CAS  PubMed  Google Scholar 

  27. Yamada, T. & Sekiguchi, Y. Cultivation of uncultured Chloroflexi subphyla: significance and ecophysiology of formerly uncultured Chloroflexi ‘subphylum i' with natural and biotechnological relevance. Microbes Environ. 24, 205–216 (2009).

    PubMed  Google Scholar 

  28. Hemp, J., Ward, L. M., Pace, L. A. & Fischer, W. W. Draft genome sequence of Ornatilinea apprima P3M-1, an anaerobic member of the Chloroflexi class Anaerolineae. Genome Announc. 3, e01353-15 (2015).

  29. Ward, L. M., Hemp, J., Pace, L. A. & Fischer, W. W. Draft genome sequence of Leptolinea tardivitalis YMTK-2, a mesophilic anaerobe from the Chloroflexi class Anaerolineae. Genome Announc. 3, e01356-15 (2015).

  30. Alonso, H., Blayney, M. J., Beck, J. L. & Whitney, S. M. Substrate-induced assembly of Methanococcoides burtonii d-ribulose-1,5-bisphosphate carboxylase/oxygenase dimers into decamers. J. Biol. Chem. 284, 33876–33882 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Knott, G. J. et al. Structural basis for AcrVA4 inhibition of specific CRISPR-Cas12a. eLife 8, e49110 (2019).

  32. Duff, A. P., Andrews, T. J. & Curmi, P. M. The transition between the open and closed states of Rubisco is triggered by the inter-phosphate distance of the bound bisphosphate. J. Mol. Biol. 298, 903–916 (2000).

    CAS  PubMed  Google Scholar 

  33. Newman, J., Branden, C. I. & Jones, T. A. Structure determination and refinement of ribulose 1,5-bisphosphate carboxylase/oxygenase from Synechococcus PCC6301. Acta Crystallogr. D. Biol. Crystallogr. 49, 548–560 (1993).

    CAS  PubMed  Google Scholar 

  34. Lu, Z., Zhao, Z. & Fu, B. Efficient protein alignment algorithm for protein search. BMC Bioinf. 11, S34 (2010).

    Google Scholar 

  35. Cleland, W. W., Andrews, T. J., Gutteridge, S., Hartman, F. C. & Lorimer, G. H. Mechanism of Rubisco: the carbamate as general base. Chem. Rev. 98, 549–562 (1998).

    CAS  PubMed  Google Scholar 

  36. Andersson, I. & Backlund, A. Structure and function of Rubisco. Plant Physiol. Biochem. 46, 275–291 (2008).

    CAS  PubMed  Google Scholar 

  37. van Lun, M., van der Spoel, D. & Andersson, I. Subunit interface dynamics in hexadecameric Rubisco. J. Mol. Biol. 411, 1083–1098 (2011).

    PubMed  Google Scholar 

  38. Schneider, G. et al. Comparison of the crystal structures of L2 and L8S8 Rubisco suggests a functional role for the small subunit. EMBO J. 9, 2045–2050 (1990).

    CAS  PubMed  PubMed Central  Google Scholar 

  39. Huynh, K. & Partch, C. L. Analysis of protein stability and ligand interactions by thermal shift assay. Curr. Protoc. Protein Sci. 79, 28.9.1–28.9.14 (2015).

    Google Scholar 

  40. Greene, D. N., Whitney, S. M. & Matsumura, I. Artificially evolved Synechococcus PCC6301 Rubisco variants exhibit improvements in folding and catalytic efficiency. Biochem. J. 404, 517–524 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  41. DePristo, M. A., Weinreich, D. M. & Hartl, D. L. Missense meanderings in sequence space: a biophysical view of protein evolution. Nat. Rev. Genet. 6, 678–687 (2005).

    CAS  PubMed  Google Scholar 

  42. Tokuriki, N., Stricher, F., Serrano, L. & Tawfik, D. S. How protein stability and new functions trade off. PLoS Comput. Biol. 4, e1000002 (2008).

    PubMed  PubMed Central  Google Scholar 

  43. Tokuriki, N. & Tawfik, D. S. Protein dynamism and evolvability. Science 324, 203–207 (2009).

    CAS  PubMed  Google Scholar 

  44. Erb, T. J. & Zarzycki, J. A short history of RubisCO: the rise and fall (?) of Nature’s predominant CO2 fixing enzyme. Curr. Opin. Biotechnol. 49, 100–107 (2018).

    CAS  PubMed  Google Scholar 

  45. Badger, M. R., Hanson, D. & Dean Price, G. Evolution and diversity of CO2 concentrating mechanisms in cyanobacteria. Funct. Plant Biol. 29, 161–173 (2002).

    CAS  PubMed  Google Scholar 

  46. Studer, R. A., Christin, P.-A., Williams, M. A. & Orengo, C. A. Stability–activity tradeoffs constrain the adaptive evolution of RubisCO. Proc. Natl Acad. Sci. USA 111, 2223–2228 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Zhou, Y. & Whitney, S. Directed evolution of an improved Rubisco; in vitro analyses to decipher fact from fiction. Int. J. Mol. Sci. 20, 5019 (2019).

  48. Wilson, R. H., Alonso, H. & Whitney, S. M. Evolving Methanococcoides burtonii archaeal Rubisco for improved photosynthesis and plant growth. Sci. Rep. 6, 22284 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  49. Frey, S. & Görlich, D. A new set of highly efficient, tag-cleaving proteases for purifying recombinant proteins. J. Chromatogr. A 1337, 95–105 (2014).

    CAS  PubMed  Google Scholar 

  50. Kane, H. J., Wilkin, J. M., Portis, A. R. & John Andrews, T. Potent inhibition of ribulose-bisphosphate carboxylase by an oxidized impurity in ribulose-1,5-bisphosphate. Plant Physiol. 117, 1059–1069 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  51. Pierce, J., Tolbert, N. E. & Barker, R. Interaction of ribulosebisphosphate carboxylase/oxygenase with transition-state analogues. Biochemistry 19, 934–942 (1980).

    CAS  PubMed  Google Scholar 

  52. Pereira, J. H., McAndrew, R. P., Tomaleri, G. P. & Adams, P. D. Berkeley Screen: a set of 96 solutions for general macromolecular crystallization. J. Appl. Crystallogr. 50, 1352–1358 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Winter, G., Lobley, C. M. C. & Prince, S. M. Decision making in xia2. Acta Crystallogr. D. Biol. Crystallogr. 69, 1260–1273 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  54. McCoy, A. J. et al. Phaser crystallographic software. J. Appl. Crystallogr. 40, 658–674 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  55. Adams, P. D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D 66, 213–221 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Afonine, P. V. et al. Towards automated crystallographic structure refinement with phenix.refine. Acta Crystallogr. D 68, 352–367 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Emsley, P. & Cowtan, K. Coot: model-building tools for molecular graphics. Acta Crystallogr. D 60, 2126–2132 (2004).

    PubMed  Google Scholar 

  58. Davis, I. W. et al. MolProbity: all-atom contacts and structure validation for proteins and nucleic acids. Nucleic Acids Res. 35, W375–W383 (2007).

    PubMed  PubMed Central  Google Scholar 

  59. Dyer, K. N. et al. High-throughput SAXS for the characterization of biomolecules in solution: a practical approach. Methods Mol. Biol. 1091, 245–258 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Hura, G. L. et al. Robust, high-throughput solution structural analyses by small angle X-ray scattering (SAXS). Nat. Methods 6, 606–612 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Rambo, R. P. & Tainer, J. A. Accurate assessment of mass, models and resolution by small-angle scattering. Nature 496, 477–481 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  62. Sali, A. & Blundell, T. L. Comparative protein modelling by satisfaction of spatial restraints. J. Mol. Biol. 234, 779–815 (1993).

    CAS  PubMed  Google Scholar 

  63. Schneidman-Duhovny, D., Hammel, M. & Sali, A. FoXS: a web server for rapid computation and fitting of SAXS profiles. Nucleic Acids Res. 38, W540–W544 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  64. Schneidman-Duhovny, D., Hammel, M., Tainer, J. A. & Sali, A. Accurate SAXS profile computation and its assessment by contrast variation experiments. Biophys. J. 105, 962–974 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Prins, A. et al. Rubisco catalytic properties of wild and domesticated relatives provide scope for improving wheat photosynthesis. J. Exp. Bot. 67, 1827–1838 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  66. Sharwood, R. E., Ghannoum, O. & Whitney, S. M. Prospects for improving CO2 fixation in C3-crops through understanding C4-Rubisco biogenesis and catalytic diversity. Curr. Opin. Plant Biol. 31, 135–142 (2016).

    CAS  PubMed  Google Scholar 

  67. Pei, J., Kim, B.-H. & Grishin, N. V. PROMALS3D: a tool for multiple protein sequence and structure alignments. Nucleic Acids Res. 36, 2295–2300 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Katoh, K., Rozewicki, J. & Yamada, K. D. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief. Bioinform. 20, 1160–1166 (2017).

    PubMed Central  Google Scholar 

  69. Potterton, E., Briggs, P., Turkenburg, M. & Dodson, E. A graphical user interface to the CCP4 program suite. Acta Crystallogr. D 59, 1131–1137 (2003).

    PubMed  Google Scholar 

  70. Krissinel, E. & Henrick, K. Inference of macromolecular assemblies from crystalline state. J. Mol. Biol. 372, 774–797 (2007).

    CAS  PubMed  Google Scholar 

  71. Krissinel, E. Crystal contacts as nature’s docking solutions. J. Comput. Chem. 31, 133–143 (2010).

    CAS  PubMed  Google Scholar 

  72. Pettersen, E. F. et al. UCSF Chimera-a visualization system for exploratory research and analysis. J. Comput. Chem. 25, 1605–1612 (2004).

    CAS  PubMed  Google Scholar 

  73. Diamond, S. et al. Mediterranean grassland soil C-N compound turnover is dependent on rainfall and depth, and is mediated by genomically divergent microorganisms. Nat. Microbiol. 4, 1356–1367 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Lavy, A. et al. Microbial communities across a hillslope–riparian transect shaped by proximity to the stream, groundwater table, and weathered bedrock. Ecol. Evol. 9, 6869–6900 (2019).

    PubMed  PubMed Central  Google Scholar 

  75. Knight, S., Andersson, I. & Brändén, C. I. Crystallographic analysis of ribulose 1,5-bisphosphate carboxylase from spinach at 2.4 A resolution. Subunit interactions and active site. J. Mol. Biol. 215, 113–160 (1990).

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

D.M.B., A.K.L. and P.M.S. acknowledge support from a Society in Science–Branco Weiss fellowship from ETH Zurich. J.H.P., P.D.A. and P.M.S. acknowledge support from the Joint BioEnergy Institute which is supported by the US Department of Energy, Office of Science, Office of Biological and Environmental Research under contract no. DE-AC02-05CH11231 between LBNL and the US Department of Energy. C.H. and J.F.B. thank A. Lavy and A. Sharrar for providing unpublished Rubisco sequences, J. West-Roberts for assistance, the Rifle IFRC/SFA 2.0 Metagenomics and Proteomics Data Analysis Project, the Allen Foundation, the Chan Zuckerberg Biohub and the Innovative Genomics Institute for support. C.H. acknowledges the Camille and Henry Dreyfus Foundation for a postdoctoral fellowship and the Joint Genome Institute CSP for sequencing. M.H. acknowledges support from the Department of Energy BER Integrated Diffraction Analysis Technologies (IDAT) program, NIGMS grant no. P30 GM124169-01 (ALS-ENABLE) for SAXS data collection at SIBYLS. D.J.O., M.A.J.P. and E.C.S. acknowledge support from the UK Biotechnology and Biological Sciences Research Council grant no. BB/I024488/1. We thank M. Hayer-Hartl (Max Planck Institute of Biochemistry, Martinsried, Germany) for the kind donation of the Syn6301-rbcL-pET11a, Syn6301-rbcLS-pET11a, pG-KJE8 and pBAD33ES/EL plasmids used in this study. Additionally, we thank N. Prywes for the kind donation of the pET28-His14-bdSUMO and pSF1389 plasmids. We also thank F. Guo and the UC Davis BioEM core facility for electron microscope images and the laboratory of J. Siegel (UC Davis Genome Center) for use of their qPCR machine for protein thermal shift experiments. We are grateful to A. Flamholz for collecting publicly available form I Rubisco kinetic data used in this study, and to A. Marinas and R. Vermon Callado for assisting with enzyme purifications. We thank K. Markel for his edits and suggestions on the manuscript.

Author information

Author notes

  1. These authors contributed equally: Jose H. Pereira, Albert K. Liu.

Authors and Affiliations

  1. Department of Plant Biology, University of California, Davis, Davis, CA, USA

    Douglas M. Banda, Albert K. Liu & Patrick M. Shih

  2. Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

    Douglas M. Banda, Albert K. Liu & Patrick M. Shih

  3. Technology Division, Joint BioEnergy Institute, Emeryville, CA, USA

    Jose H. Pereira & Paul D. Adams

  4. Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

    Jose H. Pereira, Michal Hammel & Paul D. Adams

  5. Lancaster Environment Centre, Lancaster University, Lancaster, UK

    Douglas J. Orr, Martin A. J. Parry & Elizabete Carmo-Silva

  6. Department of Earth and Planetary Science, University of California, Berkeley, Berkeley, CA, USA

    Christine He & Jillian F. Banfield

  7. Department of Environmental Science, Policy, and Management, University of California, Berkeley, Berkeley, CA, USA

    Jillian F. Banfield

  8. Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, USA

    Jillian F. Banfield

  9. Chan Zuckerberg Biohub, San Francisco, CA, USA

    Jillian F. Banfield

  10. Feedstocks Division, Joint BioEnergy Institute, Emeryville, CA, USA

    Patrick M. Shih

  11. Genome Center, University of California, Davis, Davis, CA, USA

    Patrick M. Shih

Authors
  1. Douglas M. Banda
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jose H. Pereira
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Albert K. Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Douglas J. Orr
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Michal Hammel
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Christine He
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Martin A. J. Parry
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Elizabete Carmo-Silva
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Paul D. Adams
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Jillian F. Banfield
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Patrick M. Shih
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

D.M.B., A.K.L. and P.M.S. designed experiments. D.M.B. and A.K.L. prepared all protein samples and performed all PAGE analyses and protein thermal shift experiments. M.H. performed all SEC–SAXS–MALS experiments and data analysis. J.H.P. performed X-ray crystallography data acquisition, image processing and structure determination. D.M.B. performed all structural analyses. A.K.L. performed all site-directed mutagenesis experiments. D.J.O. performed all Rubisco activity and kinetic measurements. C. H. and J.F.B performed all metagenomic and phylogenetic analyses. All authors participated in writing and manuscript preparation.

Corresponding authors

Correspondence to Jillian F. Banfield or Patrick M. Shih.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information Nature Plants thanks Martin Hagemann, Spencer Whitney and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Extended data

Extended Data Fig. 1 Distribution of form I' Chloroflexi genomes.

Maximum-likelihood phylogenetic tree of Chloroflexi using ribosomal protein S3 (rpS3) as a marker gene. To map the distribution of form I' Rubisco genes onto genomes, all MAGs were scanned for presence of both rpS3 and form I' Rubisco. MAGs containing form I' Rubisco are highlighted in orange. The scaffolds that encode RbcL vary in size substantially, ranging up to ~106 kbp in length (available as Supplementary Data). At least partial genomic context could be determined in most cases and the gene for phosphoribulokinase was adjacent. In some cases, additional CBB Cycle pathway genes were present in an operon with Rubisco, strongly supporting the function of Rubisco in this pathway. In a subset of cases, other pentose phosphate pathway genes were co-encoded. In no case was there evidence for RbcS, either on the scaffold or in the draft genome bin (where a bin was available). Gene predictions were established via a standard annotation pipeline73,74 and augmented by HMM-based profiling and domain analysis.

Extended Data Fig. 2 In form I-containing Chloroflexi operons, rbcL and rbcS are always found next to each other, unlike form I'-containing Chloroflexi operons that lack rbcS.

Fragment operons from an example set of 10 form I Rubisco-containing Chloroflexi genomes shows that rbcS is always found next to rbcL, similar to form I Rubisco found in cyanobacteria and proteobacteria11. form I' Rubisco-containing Chloroflexi genomes do not contain small subunit rbcS (Fig. 1b). Scaffold names are shown to the right of their corresponding genome fragments.

Extended Data Fig. 3 PAGE analyses.

a, Non-denaturing PAGE gel with a molecular weight marker (M, lane 1), and purified proteins of all three candidate form I' Rubisco (P. breve, 241187, and 170907) with (+) or without (-) prior activation and incubation with 10-fold molar excess of 2CABP. 241187 and 170907 denotes scaffolds B_1_S1_170907_scaffold_241187_5_Tax=RBG_16_Chloroflexi_63_12 and S_p2_S4_170907_scaffold_85440 Rubisco, respectively. b, SDS–PAGE analysis of crude cell lysate from 1) overexpression of untagged P. breve Rubisco with co-expression of GroEL/ES from pBAD33EL/ES, 2) overexpression of His14-bdSUMO-tagged P. breve Rubisco with co-expression of GroEL/ES from pBAD33EL/ES, and 3) overexpression of His14-bdSUMO-tagged P. breve Rubisco without overexpression of GroEL/ES (background GroEL/ES expression from E. coli). Without GroEL/ES overexpression, untagged RbcL comprises 8 ± 1.0 (n = 3) of the total soluble protein, which improves to 14 ± 0.5 (n = 3) when GroEL/ES overexpression in induced (see Methods). When the His14-bdSUMO tag is included on the N-terminal end of RbcL, soluble expression is 7 ± 0.8 (n = 3) and 14 ± 0.8 (n = 3) of the total soluble protein, without and with GroEL/ES overexpression, respectively. Reported values collected from n separate experiments (separately grown E. coli cultures) reflect the mean ± standard deviation.

Extended Data Fig. 4 Form I Rubisco possess a unique RbcL C-terminal extension that interacts with RbcS, which is not found in form I' Rubisco.

a, Sequence alignment of representative Rubisco RbcL sequences from forms I, I', II, II/III, IIIA and IIIb. Strictly conserved residues have a red background, residues well conserved within a group are indicated by red letters, and the remaining residues are in black letters. Gaps are represented by dots. Residue numbering along the top refers to P. breve RbcL. Symbols above blocks of sequences correspond to the secondary structure of P. breve RbcL: α, α-helix; β, β-strand; η, 310-helix. The secondary structure elements were named according to Knight et al., 199075. The positions of loop 6 (black dotted lined), the form II/III-specific Rubisco assembly domain (cyan line), and the form I-specific C-terminal extension (purple line) are indicated. The RbcX binding domain-specific to form IB Rubisco is boxed in pink. The sequence alignment was created using the UniProt RbcL sequences P22859 (Allochromatium vinosum), O85040 (Halothiobacillus neapolitanus), A0A4D4IZ26 (Zea mays), P00880 (Syn6301), Q1QH22 (Nitrobacter hamburgensis), Q3IYC2 (Rhodobacter sphaeroides), P51226 (Porphyra purpurea), Q9GGQ2 (Vaucheria litorea), E1IGS1 (Oscillochloris trichoides), A0A0P9FAF0 (Kouleothrix aurantiaca), A4WW35 (Rhodobacter sphaeroides), P04718 (Rhodospirillum rubrum), Q12TQ0 (Methanococcoides burtonii), A0A1L3Q3Y6 (Methanohalophilus halophilus), B5IH56 (Aciduliprofundum boonei), O93627 (Thermococcus kodakarensis), J1ANE7 (Methanofollis liminatans), and Q2FSY4 (Methanospirillum hungatei). The sequences for representative form I' homologues are presented in this study (Supplementary Data 1). b, Overlay of amino acid residues 408-458 of Syn6301 Rubisco (tan) with residues 415-453 of P. breve Rubisco (blue) depicting the unique RbcL C-terminal extension found in form I enzymes, but not in Rubisco homologues that do not possess RbcS. Residues R428, N429, and E430 of Syn6301 RbcL contact residues N29 and Y32 at the interface of Syn6301 RbcS (purple).

Extended Data Fig. 5 Negative-staining electron microscopy 2D images of P. breve Rubisco.

Images reflect the highest resolution data collected with activated P. breve Rubisco in phosphate buffer. The experiment was performed once (n = 1).

Extended Data Fig. 6 Extended SEC-SAXS-MALS data.

Experimental SAXS profiles (black) of P. breve Rubisco in the absence (purple) or presence (blue) of bound 2CABP is displayed with the calculated scattering from the atomistic models shown in Fig. 3c. Inset shows the Guinier plot of experimental SAXS profiles with the linear fit in the q×Rg < 1.6 limits.

Extended Data Fig. 7 Amino acid sequence alignment of Syn6301 RbcL and P. breve RbcL.

a, Structure-based sequence alignment was originally made using PROMALS3D67 using 1RBL and 6URA structures, then aligned with the complete RbcL sequences using MAFFT68. Darker shades indicate higher sequence conservation between amino acids. Syn6301 and P. breve RbcL residues involved in dimer–dimer interactions are highlighted in green and blue, respectively. Syn6301 RbcL residues involved in RbcS contacts are annotated with red stars. All contact residues were identified using CCP4 CONTACTS69. b-c, Cross-section depictions of 1RBL, without RbcS, and P. breve Rubisco highlighting dimer–dimer interactions as in panel a. d, Map of Syn6301 RbcL residues involved in RbcS interactions, highlighted in red as in panel a.

Extended Data Fig. 8 Mutating key amino acid residues at the dimer–dimer interface of P. breve Rubisco disrupts octameric oligomeric assembly.

Native PAGE gel of recombinant WT, K150A, D161A, W165A, D220A, and Y224A P. breve Rubisco. Native Mark protein ladder denoted by ‘M’. Site-directed mutants destabilize the interface between RbcL dimers leading to break down of higher-order (that is, L8) oligomers into Rubisco species with variable oligomeric state and conformations, which results in a variety of lower molecular weight migration patterns within the Native PAGE gel. Experiment was performed once (n = 1).

Extended Data Fig. 9 Site-directed mutagenesis of Syn6301 dimer–dimer interface residues imparts marginal stability in the absence of RbcS.

a, Protein thermal shift data displaying the mean fluorescent signal collected from four separate trials for WT Syn6301 RbcL, three separate mutant proteins, L158W, V154D, D349R and a combined four mutant protein, 4SDM (L158W, V154D, F217Y, and D349R). Mutations were designed to reflect homologous dimer–dimer interface residues present in P. breve Rubisco. The peaks corresponding to thermal denaturation of L8 quaternary structure are boxed, and analysis statistics are presented in the below table. Tm values represent the mean and standard deviation of n number of experiments conducted with the same protein sample. Two-tailed P-values for unpaired t test with Welch’s corrections are reported in the last column using WT Syn6301 RbcL as the reference comparison. n = number of technical replicates conducted in experiment. ns = not significant. ** P < 0.005, *** P < 0.0005. b, Native gel of purified recombinant WT and mutant Syn6301 proteins used in experiment.

Supplementary information

Supplementary Information

Supplementary note and Tables 1–3.

Reporting Summary

Supplementary Data 1

Fasta file containing protein amino acid sequences for form I' enzymes identified from MAGs.

Supplementary Data 2

Representative MAG genbank scaffolds.

Supplementary Data 3

Site-directed mutagenesis primers and synthesized candidate form I' rbcL gene sequences.

Rights and permissions

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Banda, D.M., Pereira, J.H., Liu, A.K. et al. Novel bacterial clade reveals origin of form I Rubisco. Nat. Plants 6, 1158–1166 (2020). https://doi.org/10.1038/s41477-020-00762-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41477-020-00762-4

This article is cited by

Search

Advanced search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing