C4 photosynthesis has independently evolved more than 60 times, providing one of the most widespread and effective solutions for overcoming the catalytic inefficiency of Rubisco1,2. The pathway is characterised by a biochemical CO2 concentrating mechanism that involves coordinated functioning of mesophyll (M) and bundle sheath (BS) cells within a leaf3. CO2 is initially assimilated into C4 acids by phosphoenolpyruvate (PEP) carboxylase in the mesophyll cells. These acids then diffuse to and are decarboxylated in BS cells where CO2 is concentrated. This serves to enhance Rubisco carboxylation while at the same time inhibiting Rubisco oxygenation. Passive leakage of CO2 out of the BS limits the efficiency of the system and represents an energy cost to the leaf as ATP is required to regenerate PEP4.

It has been hypothesised that low conductance to CO2 diffusion across the M and BS interface is an essential feature of the C4 photosynthetic CO2 concentrating mechanism5,6. The evolution of C4 biochemical CO2 concentration mechanism(s) has been accompanied by a suite of anatomical modifications broadly termed Kranz anatomy7, an increase in vein density8, and development of photosynthetic BS9. However, the anatomical characteristics essential for low BS conductance (gbs) are poorly understood10. It has often been speculated that interspecific diversity in gbs may in part be due to variation in the presence of secondary thickening and suberisation of the BS cell wall but diffusion path length and positioning of organelles may also be important10. In NADP-malic enzyme (ME) and PEP carboxykinase C4 subtypes, there is a deposition of the lipophilic heteropolyester suberin in the parenchymatous BS cell wall11. Chloroplasts in BS cells are centrifugally oriented only in suberised C4 species12; thus, BS suberisation is thought to function in the restriction of CO2 leakage across the M–BS interface during C4 photosynthesis13,14,15. The efficiency of the C4 photosynthetic concentrating mechanism is intimately linked to BS leakiness, ϕ, defined as the fraction of CO2 generated by C4 acid decarboxylation in the BS that subsequently leaks out. An increase in BS leakiness results in an increase in photosynthetic carbon isotope discrimination16. However, comparison of BS leakiness of species with and without suberised BS cell wall have shown no difference17, likely because of the differences in diffusion path length and organelle positioning in the species used10.

Setaria viridis (L.) P.Beauv (green foxtail millet) is an NADP-ME type C4 monocot species and its BS cell wall is suberised18. A chlorophyll fluorescence screen of a mutant population of S. viridis generated using N-nitroso-N-methylurea (NMU) was carried out to identify mutants with impaired C4 photosynthesis19. The principle of this screen was to expose NMU-treated populations to a period of low CO2 in the light; conditions in which plants with impaired C4 photosynthesis will become photoinhibited, causing a decline in chlorophyll fluorescence yield19. This can be done with high throughput in seedling trays using a chlorophyll fluorescence imaging system. One of the mutants identified (NM03966) exhibited a reduction in growth and photosynthesis19, and showed improved growth when grown at high CO2 concentrations. Bioinformatics and gene expression analyses performed in this mutant have revealed the involvement of an ATP-binding cassette subfamily G (ABCG) transporter, an important step in the synthesis of functional suberin in grasses20, that is found to be specifically expressed in C4 leaves21,22. This allowed us to examine the importance of suberin to CO2 diffusion properties of the BS cell wall and verify its importance for efficient CO2 assimilation. In addition, our results impact plant breeding programs as S. viridis is closely related to agronomically important C4 crops23 and the presence of suberin in the BS cell wall affects the digestibility of important C4 pasture grasses and their use as biofuel feed stock24,25,26.


Compromised growth in S. viridis mutant is a result of the mutation in the ABCG transporter gene

Mutant plants grew poorly in ambient CO2 concentration but when grown at 2% CO2 concentration, grew at similar height to wildtype plants (Fig. 1a and Table 1) consistent with the growth response to high CO2 concentration observed in other photosynthetically impaired NMU candidate mutants19. However even in a 2% CO2 growth environment, production of tillers and, therefore, shoot biomass remained significantly reduced in mutant plants compared to wildtype plants (Table 1). Root biomass was also significantly reduced in mutant plants compared to wildtype plants, making up to 25% of the total biomass in wildtype plants but only 13% in mutant plants (Table 1). To characterise the inheritance of the mutant phenotype, a segregating backcrossed population was generated (BC1F2). From the BC1F2 population, 25% of the segregants showed impaired chlorophyll fluorescence yield following low CO2 treatment in the light, which is characteristic of the mutant phenotype (Supplementary Fig. 1). This result suggests that a single gene or locus is responsible for the mutant phenotype. Mapping-by sequencing analysis27 identified two candidate genes from the trait-associated locus of chromosome 9 (Supplementary Fig. 2). The first one (Sevir.9G441500) had a SNP in the 3ʹUTR, whereas the second one (Sevir.9G451500) had a SNP that caused an amino acid change from a positively charged Arginine to a more polar Serine (Fig. 1b). The former gene has an unknown specific function but is assigned to a co-expression network of genes induced by ammonia treatment (Supplementary Fig. 3). The mutation in this gene, however, is judged unlikely to have an effect on gene function as the mutation is not in the coding sequence or in the promoter region. On the other hand, Sevir.9G451500 encodes for an ABCG transporter gene. Peptide sequence analysis of Sevir.9G451500 showed that it is a half transporter as it contained only one nucleotide binding domain (NBD) and transmembrane domain (TMD) arranged in reverse orientation (Supplementary Fig. 4), a unique domain arrangement characteristic of members of the ABCG subfamily28. Protein sequence and structure analysis of ABCG protein family members reveal that the mutated residue Arginine (R552) is highly conserved across members of different kingdoms (frequency of ~66%), and when substituted, it is most often by another positively charged residue, Lysine (frequency of ~16%) (Supplementary Table 1), indicative of its important functional role. Peptide sequence analysis of Sevir.9G451500 showed that R552 is located a few amino acids upstream of TMD in an amphipathic α-helix (Supplementary Fig. 4), which is previously reported to be a key component of the transmission interface essential for ABCG protein folding, ATP hydrolysis (via NBD), and substrate binding and transport (via TMD)29. Expression analysis performed using existing maize21, rice21 and S. viridis22 data showed that this particular ABCG transporter gene is highly expressed in the basal region of Zea mays and S. viridis leaves, but not in Oryza sativa leaf (Fig. 1c). This corroborates the genetic association of the ABCG transporter gene with C4 photosynthesis and leaf anatomy, most likely in BS wall suberisation as Sevir.9G451500’s direct orthologues in monocot and dicot C3 plants (Supplementary Fig. 5) have previously been reported to be involved in suberin transport30,31,32,33.

Fig. 1: Compromised growth in Setaria viridis mutant is a result of the mutation in the ABCG transporter gene Sevir.9G451500.
figure 1

a Comparison of plant growth between Setaria viridis wildtype and mutant grown at ambient condition and at 2% CO2 concentration, bars = 10 cm. Measured values of plant growth and biomass can be found in Table 1. b List of candidate mutations obtained from bioinformatics analysis of S. viridis mutant indicating Sevir.9G451500, which corresponds to ABCG transporter gene, to be likely the gene of interest. c Expression profiles of the ABCG transporter gene in leaves showing high expression in C4 NADP-ME plants, Zea mays and Setaria viridis, but not in C3 plant, Oryza sativa. Z. mays and O. sativa leaf expression profiles were generated in eFP61 using existing data21. RPKM data used to generate S. viridis leaf expression profile were mined from previous data22 and drawn according to the eFP colour scale.

Table 1 Comparative analysis of different plant and leaf properties between Setaria viridis wildtype and mutant grown at 2% CO2 environment.

Mutation in ABCG transporter gene impedes proper BS suberisation in S. viridis leaf

Suberised BS in leaves of NADP-ME C4 grasses is characterised by the presence of a dark, osmiophilic band deposited in the outer tangential wall and radial wall of the BS–M interface20 that can be visualised under an electron microscope. This contrasts with periderm and suberised cork cells, which have distinct layers of alternating light and dark lamellae corresponding to aliphatic suberin compounds and aromatic lignin-like compounds, respectively34,35. Transmission electron microscopy (TEM) performed on wildtype and mutant leaf tissues revealed disrupted and thinner suberin lamellae in the BS cell wall of mutant compared to wildtype (Fig. 2a). Consequently, there was a significant reduction in BS cell wall thickness of mutant leaf relative to the wildtype leaf (Table 1). Disrupted dark lamellae are typically associated with defects in the aliphatic component of suberin31,35. Nile Red staining, which targets the aliphatic suberin compounds36,37,38, showed a lower signal in the BS of mutant leaves compared to wildtype (Fig. 2b) consistent with the reduced Fluorol Yellow staining in the mutant compared to the wildtype (Supplementary Fig. 6). Since the polyaromatic moiety of suberin shares similarities with lignin34, staining after clearing using lignin stain (Basic Fuchsin)37 was performed. Basic Fuchsin staining showed the presence of lignin around BS of both wildtype and mutant leaves (Fig. 2c), most probably from the lignocellulosic tertiary wall20 but also likely contributed too by the hydroxycinnamic acids39, ferulate and coumarate, which are lignin-like aromatic compounds abundant in suberin40. To further investigate specific changes between the aliphatic and aromatic components of suberin in mutant leaves, particularly in the BS, gas chromatography/mass spectrometry (GC/MS) was performed. GC/MS analysis of suberin monomers obtained after BF3-methanol depolymerisation of solvent-extracted residue41 from leaf and isolated BS strands revealed a significant reduction of up to 50% in the aliphatic suberin compounds (C16–C26) in mutant relative to wildtype plants (Fig. 3 and Supplementary Table 2). The reduction in aliphatic suberin monomers in mutant plants is mainly attributed to the BS as evidenced by the proportional increase in monomer concentrations obtained from the isolated BS strands compared to the leaf (Fig. 3 and Supplementary Table 2). In addition, there was no significant difference between the cutin layer of wildtype and mutant leaves (Supplementary Fig. 7) suggesting that cutin deposition in leaves of mutant plants is not affected by the mutation. There was no significant difference between wildtype and mutant aromatic suberin monomers in leaf and isolated BS strands (Supplementary Table 2) and staining and GC/MS analyses performed in roots also showed no significant difference between wildtype and mutant plants (Supplementary Figs. 6 and 8 and Supplementary Table 2). Together, these results suggest that the mutation in the ABCG transporter gene, Sevir.9G451500, negatively affected BS suberisation in S. viridis leaves resulting in the absence of functional suberin lamellae around the BS. No significant change was observed in other C4 leaf-associated anatomical traits examined, which included BS surface area to leaf area ratio (Sb), M surface area to leaf area ratio (Sm), and M–BS plasmodesmata density (Table 1 and Supplementary Fig. 9); there was however an increase in stomatal density (Table 1).

Fig. 2: Mutation in ABCG transporter gene Sevir.9G451500 impedes proper bundle sheath suberisation in Setaria viridis leaf.
figure 2

a Electron micrographs of transverse leaf sections of Setaria viridis wildtype and mutant showing disrupted and thinner suberin lamellae (black arrows) in mutant bundle sheath (BS) cell wall. M, mesophyll; *, plasmodesmata. Bars = 0.5 µm. b Orthogonal view of z-stacks of cleared leaf tissue of S. viridis wildtype and mutant stained with Nile Red (magenta, aliphatic component of suberin) and Calcofluor White (cyan, cell wall) showing decreased level of aliphatic suberin staining in mutant bundle sheaths (see Supplementary Videos 1 and 2). Line graphs show the profile of Nile Red fluorescence along the leaf tissue, with wildtype showing peaks where bundle sheaths (white arrows) are present. Bars = 50 µm. c Transverse hand section of leaf of S. viridis wildtype and mutant stained with Basic Fuchsin (yellow, lignin) and Calcofluor White (cyan, cell wall) showing unaltered lignin deposition in mutant leaf. Bars = 50 µm.

Fig. 3: Mutation in ABCG transporter gene Sevir.9G451500 affects the synthesis of aliphatic suberin monomers in Setaria viridis mutant.
figure 3

Relative suberin monomer composition of leaf and bundle sheath strands of Setaria viridis wildtype and mutant showing reduced aliphatic monomers in mutant, n = 5. Note the difference in y-axis scale between leaves and bundle sheath strands plots. Statistically different values according to one-way analysis of variance are denoted by * at p < 0.05, ** at p < 0.01 and *** at p < 0.001. Numerical values of the relative average concentration expressed as μg monomer per g tissue, standard error and p-value according to one-way analysis of variance of each suberin monomer of S. viridis wildtype and mutant leaves and bundle sheath strands after BF3-MeOH depolymerisation are provided in Supplementary Table 2. Individual measured values are provided in Supplementary Data.

Absence of functional suberin lamellae resulted in leaky BS in S. viridis mutant

CO2 assimilation rates were reduced in the mutant plants compared to wildtype plants (Fig. 4a). Although the initial slope of the CO2 response of CO2 assimilation is similar for mutant and wildtype plants, CO2 assimilation rates of the mutant fail to increase to the same degree as wildtype above an intercellular CO2 of 100 µbar. The reduced CO2 assimilation rate of the mutant is also apparent in the light response of CO2 assimilation rate (Fig. 4b). Stomatal conductance is also reduced in the mutant plants (Fig. 4c), but the intercellular CO2 partial pressure is similar between mutants and wildtype leaves so that reduced CO2 access is not the cause of the reduction in CO2 assimilation rates. The reduction in CO2 assimilation rates cannot be explained by reduced photosynthetic biochemistry as the in vitro PEPC, Rubisco and carbonic anhydrase activities were similar between wildtype and mutants (Table 1). The reduction of stomatal conductance in the mutant was observed despite increased stomatal density (Table 1) pointing to a possible mechanical effect of reduced suberin on stomatal opening.

Fig. 4: Absence of functional suberin lamellae resulted in leaky bundle sheath in Setaria viridis Sevir.9G451500 mutant.
figure 4

a CO2 assimilation rate over a range of intercellular partial pressures of CO2, and b CO2 assimilation rate and c stomatal conductance over a range of irradiances of Setaria viridis wildtype and mutant, n = 4. d Time course of CO2 assimilation rate of detached S. viridis wildtype and mutants leaves after feeding with 2–4 mM DCDP measured at 400 μbar CO2, and e subsequent measurements of CO2 response curves of DCDP-fed leaves over a range of pCO2, n = 4. The initial slope of the CO2 response curve was used to calculated bundle sheath conductance (gbs)42. For wildtype gbs = 2.8 ± 0.3 mmol m−2 s−1 bar−1 and for the suberin mutant gbs = 7.4 ± 0.7 mmol m−2 s−1 bar−1. f Carbon isotope discrimination, ∆, as a function of the ratio of intercellular to ambient CO2, Ci/Ca in S. viridis wildtype and mutant. Measurements were made at 2% O2, 380 µmol mol−1 CO2, leaf temperature of 25 °C, irradiance of 1500 µmol quanta m−2 s−1 and relative humidity of 55% using combined tuneable diode laser spectroscopy and gas exchange measurements, n = 8. The lines depict the predicted theoretical relationship between ∆ and Ci/Ca during C4 photosynthesis at infinite gm at a leakiness, ϕ = 0.34 and 0.29 (∆ = 4.3 + (−5.7 − 4.3 + 27.2 × ϕ)Ci/Ca)16,57. g CO2 assimilation rate of S. viridis wildtype and mutants measured over a range of intercellular partial pressures of CO2 made consecutively at 21%, 2% and 10% O2, n = 4. All measurements were done using the youngest fully expanded leaf of 4-week-old plants grown at 2% CO2 environment. Each symbol corresponds to the mean and the error bars as ±SE; n denotes the number of plants measured. Individual measured values are provided in Supplementary Data.

BS conductance to CO2 diffusion of mutant compared to wildtype was also measured. To estimate BS conductance to CO2 diffusion directly, the PEPC inhibitor 3,3-dichloro-2-(dihydroxyphosphinoylmethyl) propenoate (DCDP) was used to inhibit the C4 cycle function of C4 photosynthesis of the wildtype and mutant leaves6 (Fig. 4d). It is noteworthy that it was not possible to inhibit CO2 assimilation rate completely in mutant leaves presumably due to direct CO2 fixation by BS Rubisco. After PEPC inhibition, measured CO2 response curves were used to estimate BS conductance to CO2 diffusion, gbs, from the initial slopes of the curves42 (Fig. 4e). This showed that gbs has more than doubled in the mutant compared to the wildtype. Measurement of carbon isotope discrimination as a measure of BS leakiness, ϕ (defined as the fraction of CO2 generated by C4 acid decarboxylation in the BS that subsequently leaks out), also showed a significant increase in the mutant relative to the wildtype (Fig. 4f and Table 1), consequently increasing the oxygen sensitivity of the CO2 assimilation rate in the mutant (Fig. 4g). This increased BS leakiness in the mutant was corroborated by quantum yield measurements, which showed significant reductions in the mutant compared to the wildtype commensurate with a loss of photosynthetic efficiency (Table 1).


We have investigated a C4 photosynthesis mutant (NM03966), identified using chlorophyll fluorescence-based high throughput phenotyping platform, for its underlying genetic alteration and mapped an ABCG transporter gene, Sevir.9G451500, as the causal gene. Our phylogenetic analysis revealed that the direct orthologues of this gene in monocot and dicot plants/crops have previously been reported in suberin transport. Our gene expression analysis also revealed that this gene is highly expressed in NADP-type C4 leaves but not in C3 leaves. We have used TEM, two recognised suberin stains, and GC/MS to confirm the reduction in leaf suberin, particularly in the BS cells, of Sevir.9G451500 or ABCG transporter gene mutant. The reduction in suberin is leaf-specific and does not affect suberin in the roots, suggesting that most of the differences in growth observed in mutant plants compared to wildtype plants are due to reduced CO2 assimilation rate. We propose from this study that the discontinuous suberin lamellae in the BS cell wall in the mutant allowed CO2 to escape from the BS through diffusion across the cell wall, disrupting the CO2 concentrating mechanism in the leaves of S. viridis. This was confirmed by direct measurements of BS conductance, gbs, which had more than doubled in the mutants. This led to a significant reduction in CO2 assimilation rate and decreases in plant growth and biomass in mutant plants. The disrupted BS suberin layer also resulted in increased O2 sensitivity of CO2 assimilation. If the BS CO2 partial pressure is calculated using the gbs values in Fig. 4e and the equations described in Pengelly et al.43 (Eqs. 6–8), a value of 4635 µbar is obtained for the wildtype and 1693 µbar for the mutant. The latter is only barely above the KmCO2 for a C4 plant Rubisco44 such as S. viridis and is commensurate with the oxygen sensitivity of photosynthesis observed in this mutant. While the physiological phenotypes of this mutant are largely predicted by models of C4 photosynthesis45 (Supplementary Fig. 10), the decreased CO2 assimilation rate in the mutant, particularly at high CO2 and irradiance, is greater than can be predicted from an increase in gbs alone, suggesting that other metabolic impairments are occurring (comparison of Fig. 4g and Supplementary Fig. 10). The moderate increase in carbon isotope discrimination observed here would indicate that BS leakiness increased by only 17%. As leakiness, ϕ, is defined as

$$\phi = g_{{\mathrm{bs}}}\left( {C_{{\mathrm{bs}}} - C_{\mathrm{m}}} \right)/V_{\mathrm{p}}$$

where Cm and Cbs are M and BS CO2 partial pressures and Vp is the rate of PEP carboxylation, one must assume that some impairment in the rate of PEP carboxylation has occurred, restricting the capacity of the M reactions to respond and elevate CO2 supply to the BS. As the extractable activity of PEPC and Rubisco from the mutant plants did not differ from that found for the wildtype plants (Table 1), either the provision of PEP to PEP carboxylase must become limiting at higher fluxes (potentially via a limitation in ATP supply) or posttranslational downregulation of enzyme activity in the M is occurring. Notably, in transgenic Flaveria bidentis with reductions in Rubisco activity due to RbcS gene suppression, greater BS CO2 leakiness occurred due to elevated BS CO2. While Vp was reduced in these plants, this was not commensurate with the reduction in net CO2 assimilation46. In the case of Flaveria plants, where NADP-ME activity was reduced by gene suppression43, a reduction in BS leakiness to CO2 was observed as predicted. However, the amount of both Rubisco and PEPC actually increased despite a substantial decrease in Vp being observed. While we have not previously had access to C4 plants where BS cell wall properties were genetically altered rather than cell-specific enzyme activities, taken together these experiments suggest that a variety of regulatory processes may be occurring to match BS and M biochemical fluxes and minimise CO2 leakage.

To conclude, the S. viridis ABCG transporter gene Sevir.9G451500 mutant provided the opportunity to analyse the effect BS cell wall properties have on the C4 photosynthetic CO2 concentrating mechanism. We have shown that the disruption of the suberin lamellae has increased BS conductance to CO2, which resulted in reduced CO2 assimilation rates due to reduced BS CO2 partial pressure. Anatomical and biochemical assays showed few other differences between mutant and wildtype plants other than stomatal function, which is accounted for in gas exchange measurements. This work experimentally demonstrates the importance of a functional suberin lamella around the BS for efficient C4 photosynthesis in the leaves of C4 species like S. viridis, which have centrifugally oriented chloroplasts, and represents a central discovery for understanding the C4 photosynthetic mechanism, the evolution of C4 photosynthesis and the engineering of this process into C3 crops.


Plant material and growth conditions

M5 seeds were grown in Australia between March and August 2019. The seeds were germinated in garden soil mix fertilised with Osmocote (Scotts, Australia) in small containers before being transferred to individual 2 L pots. Plants were grown in controlled environmental chambers, irradiance 500 µmol photons m−2 s−1, 16-h photoperiod, 28 °C day, 24 °C night, 2% CO2. Pots were watered daily.

Plant growth and biomass measurements

The whole plant was removed from the pot and the roots were washed with water to remove any adhering soil. Plant height was measured from the base of the shoot using the main tiller. After counting the number of tillers per plant, the roots and shoots were dried separately at 80 °C oven for 5 days and weighed.

Generation of segregating population and DNA sequencing of bulked segregants

Homozygous mutant M5 plants were crossed with wildtype to generate F1 heterozygous lines. The F1 lines were selfed to produce segregating F2 populations (BC1F2). From a BC1F2 population of 300 plants (Supplementary Fig. 1), equal quantities of DNA were pooled from 45 individual plants exhibiting the suberin phenotype (homozygous mutant pool) and 54 individuals without the suberin phenotype (pool of azygous or hemizygous lines). DNA was also pooled from 50 individual WT plants (WT pool). The genomic DNA was extracted from young leaves mid-tillering using a cetyltrimethylammonium bromide (CTAB) protocol47. The DNA quantity and quality were evaluated using a Nanodrop ND-8000 spectrophotometer (Thermo Scientific, Waltham, MA, USA) and agarose electrophoresis. The three samples were sequenced using Illumina HiSeq2000 platforms at The Beijing Genome Institute (BGI Tech Solutions (Hongkong) CO, Limited, Shenzhen, China). The reads were paired-end (PE) of size 125 base pairs. Number of paired-end reads generated were ~108.1 million for WT pool, ~91 million for azygous pool and ~107.3 million for mutant pool yielding 23–33 Giga-bases of genomic sequence with a genome coverage of 45–65X.

Variant discovery

The raw sequence data were processed so that reads/bases with poor quality are either trimmed or filtered using Trimmomatic v0.32 (ref. 48). The minimum Phred quality score was set to 20, and reads containing partial/complete Illumina adaptor sequences were also trimmed. The processed reads were aligned against the S. viridis reference genome (version 1.1 from Phytozome database) using BWA aligner version 0.7.12 (ref. 49). The alignment was improved by discarding the duplicate read pairs with the PICARD tool (, and re-calibration of base quality using very high-quality variants as a gold standard using the GenomeAnalysisTK (GATK-3.7-0) tool50. Variant calling was also done by the same tool such that alleles were first called at all genomic positions, followed by variant calling51.

Filtering of variants to identify candidates

Variants with an allele frequency of 0.3 or less were considered to result from improper alignment of minority reads, thus, removed from the analysis. Only variants occurring in the pooled mutant samples with at least 10 reads and a genotype quality (GQ) of called variants of 30 or above were considered for downstream analysis. In order to discover allele(s) which were present in all individuals (that were pooled), the frequency of induced mutations (mutant alleles) in the paired samples were plotted along chromosome position. Theoretically, a mutation with allele frequency of 1 in the mutant pool should display a frequency of 0.5 or less in the azygous pool. Genomic regions/loci harbouring mutations qualifying above filters were extracted, and were called candidate mutations. Variants with an allele frequency of 1 were checked to see if neighbouring ones showed a typical linkage pattern.

Causal gene discovery

Candidate mutations with an allele frequency of 1 in the mutant pool were annotated with the S. viridis annotation from Phytozome 12 ( Mutations within a gene leading to alterations to protein structure were classified as candidate genes.

Suberin and lignin staining

Tissue from the widest portion of the third fully expanded leaf of 10-day-old plant was fixed with 4% paraformaldehyde for 1 h at room temperature, sectioned, and stained along with transverse sections of the root37. Aliphatic suberin staining was performed using 0.05% Nile Red in ClearSee solution (10% (w/v) xylitol, 15% (w/v) sodium deoxycholate, 25% (w/v) urea in water) while lignin staining used 0.2% Basic Fuchsin in ClearSee solution; 0.1% Calcofluor White was used in combination with Nile Red and Basic Fuchsin to visualise cell walls. Nile Red-stained and Basic Fuchsin-stained tissues and sections were mounted onto glass slides with ClearSee solution. Fluorol Yellow staining was performed according to Yadav et al.31. Slides were examined with a Leica SP8 multiphoton confocal microscope (Leica Microsystems). Nile Red was imaged at 561 nm excitation wavelength and detected at 600–620 nm. Basic Fuchsin was imaged at 561 nm excitation wavelength and detected at 600–650 nm. Fluorescence from Calcofluor White-stained cell walls was detected at 434–445 nm following excitation at 405 nm. Fluorol Yellow was imaged at 514 nm excitation wavelength and detected at 516–593 nm.

Anatomical measurements

Sample preparation for light microscopy and electron microscopy was performed using the middle portion of the youngest fully expanded leaf of 14-day-old plants18. Light micrographs used to calculate BS surface area per unit leaf area (Sb) and M surface area exposed to intercellular airspace (Sm)52 were obtained using Leica DM5500 compound microscope (Leica Microsystems). BS and M cell wall thickness were measured using electron micrographs of the transverse leaf sections imaged under Hitachi 7100 transmission electron microscope (Hitachi High Technologies America). Pit field area per cell interface area was used as a measure of plasmodesmata density8,18. Stomatal measurements were made on the abaxial side using regions close to the midrib within the widest portion of the youngest fully expanded leaves. Stomatal imprints were obtained as described53 and images were captured under 10× objective using Leica DM5500 compound microscope. Stomatal density (number of stomata/unit leaf area) and stomatal index (proportion of epidermal cells that are stomata) were quantified. All anatomical measurements were performed using ImageJ.

GC/MS sample preparation

Isolated BS strands54 (2 mL or ~150 mg dry weight per replicate), mature leaf tissue devoid of midrib (250 mg fresh weight per replicate) and mature root tissue (250 mg fresh weight per replicate) from 3-week-old plants were snap-frozen in liquid nitrogen and freeze-dried for 3 days before grinding into a powder. Powdered tissue was extracted in 5 mL of hot isopropanol overnight and thoroughly delipidated in 2 mL solvent sequence of 2:1, 1:1, 1:2 dichloromethane:methanol and methanol (~2 h each). Solvent-extracted residue, which contains the suberin fraction, was oven-dried at 37 °C overnight. Depolymerisation of suberin was performed by resuspending the dried delipidated residue with 5 µL of internal standard mix (10 mg mL−1 heptadecanoic acid, 1 mg mL−1 pentadecanol, and 1 mg mL−1 C15-hydroxypentadecanoic acid in methanol) into 2 mL of 10% BF3-methanol (Sigma 33020-U) at 60 °C for 24 h41. To recover the fatty acid methyl esters, 4 mL of 2.5% (w/v) aqueous NaCl and 1.5 mL of methyl tert-butyl ether (MTBE) were added, followed by centrifugation at 800 × g for 5 min to facilitate phase separation. The organic extract was washed with 1 mL of 100 mM Tris-HCl pH 8.0 before drying in CentriVap concentrator (Labconco) at room temperature setting for 2 h. Addition of 5 µL alkane mix (1 mg/mL solutions of n-dodecane, n-pentadecane, n-nonadecane, n-docosane, n-octacosane, n-dotriacontane, n-hexatriacontane in anhydrous pyridine) followed by derivatisation of free hydroxyl and carboxyl groups with 25 µL of N-methyl-N-(trimethylsilyl)trifluoroacetamide (Sigma 69479) at 60 °C for 60 min were done prior to GC/MS analysis.

GC/MS analysis

A single quadrupole GC/MSD instrument (Agilent Technologies, Palo Alto, CA, USA) consisting of a 7890A series gas chromatograph with split/splitless injector and a 5975C inert XL MSD mass selective detector (Triple-Axis Detector) retrofitted with a MPS 2 Gerstel Multipurpose Sampler with liquid injection capability (Gerstel GmbH & Co. KG, Germany) was used for GC/MS analysis. GC conditions were as follows: 40 m (30 m separation phase + 10 m integrated guard column) × 250 µm ID × 0.25 µm film thickness Varian Factor Four 5 ms capillary column (CP9013); helium carrier gas; constant column gas flow 1 mL min−1; total run time 59 min; splitless injection; inlet temperature 230 °C; septum purge flow 3 mL min−1; gas saver mode on after 2 min; purge flow to split vent 20 mL min−1 at 1 min; initial oven temperature 70 °C, held for 1 min then ramped at 5 °C min−1 to 325 °C and held for 7 min; transfer line temperature 250 °C. MS conditions were as follows: electron impact ionisation with 70 eV energy; source temperature 230 °C; quadrupole temperature 150 °C; solvent delay 4.2 min; normal scanning; scan range 40–600 m/z; threshold zero; A/D samples 2; electron multiplier in gain mode with gain of 1.0. Instrument control and data acquisition were handled by MassHunter GC/MS Acquisition (version B.07.04.2260; Agilent Technologies, Palo Alto, CA, USA) with Maestro 1 plugin (version; Gerstel). The MSD was pre-tuned against perfluorotributylamine (PFTBA) mass calibrant using the “atune.u” autotune method.

GC/MS data analysis

Agilent MassHunter software (version 10.0) was used for data analysis. The NIST/EPA/NIH Mass Spectral Library (version 2017) was used for mass spectral matching (≥70% confidence) and peak annotation. Peak for methyl 24-hydroxytetracosanoate was annotated using published information55. Peak areas of internal standards and identified suberin monomer compounds were quantified from extracted ion chromatograms based on their quantifier ion (Supplementary Table 3). To get the relative monomer concentration expressed as μg monomer per g tissue, monomer mass was quantified using the appropriate internal standard (Supplementary Table 3) and then normalised to the amount of tissue used in each replicate.

Gas exchange measurements

All gas exchange measurements were made on youngest fully expanded leaf of 4-week-old plants grown at 2% CO2 environment. CO2 response curves of CO2 assimilation rate were measured with a LI-6800 portable photosynthesis system (LI-COR Biosciences, USA) at a leaf temperature of 25 °C, irradiance 1500 µmol quanta m−2 s−1, relative humidity of 55%, 21% O2 and varying reference CO2 concentration (0, 50, 75, 100, 200, 300, 400, 600, 800, 1000, 1200 µmol mol−1). For oxygen sensitivity of CO2 response curves of CO2 assimilation rate, measurements were made at same conditions but at three O2 concentrations of 21%, 2%, 10% in that order. Light response curves were measured at a leaf temperature of 25 °C, relative humidity of 55%, 21% O2, ambient CO2 of 380 µmol mol−1 and varying irradiance (2000, 1500, 1000, 750, 500, 300, 200, 150, 100, 75, 50, 25, 0) starting at 2000 µmol quanta m−2 s−1 and then step-wise decreasing irradiance at 3-min intervals. The quantum yield was calculated from the slope of the low light measurements (0–200 µmol quanta m−2 s−1). Gas exchange measurements combined with tuneable diode laser measurement were made56 for 13C isotope discrimination. Measurements were made at 2% O2, 380 µmol mol−1 CO2, leaf temperature of 25 °C, irradiance of 1500 µmol quanta m−2 s−1 and relative humidity of 55%. Leakiness, defined as the rate of CO2 leak rate out of the BS over the rate of CO2 delivery to the BS, was calculated from the simplest form of the equation relating leakiness to carbon isotope discrimination, ∆16,57:

$$\Delta = 4.3 + \left( { - 5.7 - 4.3 + 27.2 \times \phi } \right)C_{\mathrm{i}}/C_{\mathrm{a}}.$$

PEPC inhibitor DCDP feeding and estimation of BS conductance, g bs

DCDP feeding in detached leaves and estimation of BS conductance (gbs) were made by the first method described in ref. 42.

Biochemical measurements

Measurements of Rubisco, PEPC and carbonic anhydrase activity were made as described58. Rubisco catalytic site content were measured for both non-DCDP-fed plants and DCDP-fed plants59,60.

Statistics and reproducibility

Significance analysis of all experimental data between wildtype and mutant were determined according to two-sample t-test or one-way analysis of variance using OriginPro 9.1 (OriginLab Corporation). No outliers were excluded in any statistical analysis. Figures were generated using OriginPro 9.1 (OriginLab Corporation) and Microsoft Powerpoint. Details of sample size or replication number were listed in Table 1 and described in the figure legends.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.