Missense mutations in a transmembrane domain of the Komagataeibacter xylinus BcsA lead to changes in cellulose synthesis

doi:10.21203/rs.2.9716/v1

Background

Cellulose is synthesized by an array of bacterial species. Komagataeibacter xylinus is the best characterized as it produces copious amounts of the polymer extracellularly. Despite many advances in the past decade, the mechanisms underlying cellulose biosynthesis are not completely understood. Elucidation of these mechanisms is essential for efficient cellulose production in industrial applications.

Results

In an effort to gain a better understanding of cellulose biosynthesis and its regulation, cellulose crystallization was investigated in K. xylinus mutants resistant to an inhibitor of cellulose I formation, pellicin. Through the use of forward genetics and site-directed mutagenesis, A449T and A449V mutations in the K. xylinus BcsA protein were found to be important for conferring high levels of pellicin resistance. Phenotypic analysis of the bcsAA449T and bcsAA449V cultures revealed that the mutations affect cellulose synthesis rates and that cellulose crystallinity is affected in wet pellicles but not dry ones.

Conclusions

A449 is located in a predicted transmembrane domain of the BcsA protein suggesting that the structure of the transmembrane domain influences cellulose crystallization either by affecting the translocation of the nascent glucan chain or by allosterically altering protein-protein interactions.

Applied & Industrial Microbiology

Komagataeibacter xylinus

pellicin

BcsA

crystallinity

Background

Cellulose, an abundant glucan polymer, is synthesized by organisms belonging to a variety of phylogenetic domains (1). In nature, the majority of plants and the bacterium Komagataeibacter xylinus (formerly Gluconacetobacter xylinus), synthesize a crystalline form designated cellulose I (2). The glucan chains in cellulose I are arranged parallel to one another and assembled side-by-side forming structures known as microfibrils (3,4). Cellulose I exists in two allomorphs; Iα (triclinic) and cellulose Iβ (monoclinic), which can be differentiated using solid-state ¹³C NMR (5). The two allomorphs are distinguished from one another by their crystal packing hydrogen bond interactions and molecular conformation, which alter the physical characteristics of the polymer (6). One cellulose microfibril may contain both types of allomorphs; with the Iβ form dominant in higher plants and the Iα form dominant in bacteria and algal species (7). An alternative form of cellulose, known as cellulose II, can be obtained through either industrial mercerization (alkali treatment) or regeneration (solubilization and subsequent recrystallization) (5). In cellulose II, the glucan chains are arranged in an antiparallel conformation (8); each glucose residue has an additional hydrogen bond which makes it a more thermodynamically stable conformation. In contrast to cellulose I, cellulose II is made by very few organisms, such as the gametophyte cells of the marine alga of the genus Halicystis and gram-positive bacteria of the genus Sarcina (1).

In bacteria, cellulose is synthesized as an extracellular polysaccharide via a single polymerization step that uses uridine diphosphoglucose (UDP-glucose) as substrate which undergoes self-assembly at the site of biosynthesis (9). This process is driven by integral membrane glycosyltransferases (GTs) that couple the elongation of the polymer with the translocation of the product outside the cell (10). A single cell of Komagataeibacter xylinus can polymerize up to 200,000 glucose molecules into β-1,4 glucan chains every second (11). The synthesis of bacterial cellulose (BC) is precisely regulated by a diverse number of enzymes and regulatory proteins. Synthesis occurs in the periplasm by cellulose synthesizing complexes (CSCs) or terminal complexes (TCs), which are associated with outer membrane pores organized linearly along the long axis of the cell (12–14). Protofibrils are thought to be assembled into ribbon-shaped microfibrils that elongate while remaining associated with the cell envelope, even during cell division, giving rise to BC or pellicle (14). The polymerization of cellulose is catalyzed by cellulose synthase (CS) without the formation of intermediates (15).

K. xylinus possesses a cellulose synthase operon (bcs operon) composed of three to four genes, depending on the strain or subspecies: bcsAB (or bcsA and bcsB), bcsC, and bcsD (16). The protein product encoded by bcsA is an integral membrane protein that contains multiple transmembrane (TM) domains; four N-terminal and four C-terminal TM helices separated by an extended intracellular loop between helices 4 and 5 that forms the glycosyltransferase (GT) domain (10) that includes a conserved motif with three spaced aspartates followed by a pentapeptide sequence motif (QxxRW) characteristic among processive GTs like hyaluronan, chitin and alginate synthases (16,17). The GT domain of BcsA contains seven β-strands surrounded by seven α-helices. The narrow channel for cellulose translocation is formed by the TM helices 3 to 8 and appears to accommodate 10 glucose residues of the translocating glucan chain (10). Most inverting GTs require an essential divalent cation for catalysis. The cation is coordinated by the conserved Asp-X-Asp (DXD) motif at the active site to stabilize the nucleotide diphosphate leaving group during glycosyl transfer (10). The activity of BcsA is stimulated by an allosteric regulator, 3’, 5’-cyclic diguanylic acid (c-di-GMP), which interacts with the PilZ domain located at the C-terminus of the BcsA, next to the GT domain (18,19). Binding of the c-di-GMP causes a conformational change in the PilZ domain disrupting a specific Arg-Glu salt bridge, which results in the displacement of a “gating loop” that allows UDP-glucose to bind (19).

In contrast, the product of the bcsB gene is a predominantly β-stranded periplasmic protein with a single transmembrane anchor that interacts with BcsA (10). The BcsB protein contains four domains: two jellyroll domains, which show high similarity to carbohydrate binding domains (CBDs), and two flavodoxin-like folds (10). Although BcsB is essential for catalysis, only the interactions of its C-terminal TM anchor and an amphipathic helix seem to be necessary to stabilize the TM region of BcsA for catalysis (19). In addition, BcsB is thought to be required to guide cellulose across the periplasm toward the outer membrane via the two carbohydrate-binding domains (CBDs) (10). While the functions of BcsC and BcsD have not been fully elucidated, they both influence cellulose crystallinity. For example, BcsC is predicted to form a β-barrel porin located in the outer membrane, which is preceded by a relatively extensive periplasmic domain carrying tetratricopeptide repeats which may be involved in complex assembly (20,21). On the other hand, BcsD, for which the crystal structure has been elucidated, is thought to function as a periplasmic channel for the nascent cellulose strand (22,23). Indeed, the isolation of K. xylinus bcsD mutants, which form smooth colonies and produce reduced amounts of cellulose in culture, suggests that BcsD is involved in cellulose crystallization (9). Recently, Sajadi et al. (24) showed that heterologous expression of bcsD in Escherichia coli increased the crystallinity but did not affect the yield of BC. In addition to the cellulose synthesis operon genes, ancillary genes have been implicated in cellulose biosysnthesis. One of these genes, bcsZ (formerly cmcax), which is located upstream of the cellulose synthase operon, encodes an endo-β-1,4-glucanase (BcsZ, formerly CMCax) which possesses cellulose hydrolyzing activity that is essential for BC production (25). In addition, bcsH (formerly ccpax), also located upstream of the bcs operon, encodes a cellulose complementing protein. The function of BcsH is not well understood, but it has been suggested to be important for cellulose crystallization (26). Mutations in the bcsH locus result in a significant decrease in cellulose production (27). A downstream region of the operon which encodes an enzyme with exo-1,4-β-glucosidase activity (BglAx) towards cellotriose or larger cello-oligosaccharides also leads to significant decrease in cellulose production when mutated (28). The precise role of BglAx is, however, still unknown (27).

In a previous study, we used a chemical genetic approach to identify pellicin, a potent inhibitor of cellulose pellicle formation that exerts its effect extracellularly (29). An important property of pellicin is that it can inhibit cellulose crystallization without disrupting cell growth (29). In addition, pellicin does not inhibit cellulose synthase activity directly since crude membrane preparations from K. xylinus cells grown in pellicin-containing medium show increased cellulose synthesis compared to untreated membrane preparations (29). These and other features of pellicin suggest that it allows normal cellulose II biosynthesis assembly but inhibits the assembly of cellulose I. In order to better understand the mechanism of action of pellicin, we have conducted a forward genetic screen aimed at identifying pellicin-resistant mutants. Our current findings indicate that in K. xylinus, one indirect target for pellicin activity is the BcsA protein.

Forward genetic screening identifies mutant with resistance to pellicin

Crystallinity of cellulose pellicles formed by K. xylinus is greatly reduced in the presence of pellicin (29). In an effort to further investigate cellulose crystallization during biosynthesis, we conducted a forward genetic screen aimed at identifying pellicin resistant (plr) mutations. To do this, we mutagenized a K. xylinus culture with ethyl methanesulfonate (EMS); 4 million mutagenized cells were initially screened in medium containing 10 µM pellicin. Among the mutants that were isolated, three were able to produce a thick pellicle at concentrations of pellicin exceeding 10 µM (Supplemental Table 1). Among these plr mutants, we focused on plr15 for further analysis, as it had the highest resistance.

As a measure of crystalline cellulose, we determined the cellulose content of plr15 and wild-type pellicles formed in the absence and presence of 10 µM pellicin from static cultures. Total cellulose content was measured using an acetic/nitric acid extraction which solubilizes all sugar polymers with the exception of crystalline cellulose (30). The pellicles produced by plr15 under these conditions were significantly reduced (approximately 23%) compared to those formed in SH medium lacking pellicin, indicating that plr15 is not pellicin-blind (Supplemental Figure 1). Although this analysis does not provide structural information about the cellulose formed by plr15, it does suggest that the mutation has an effect on crystalline cellulose production in the presence of pellicin.

The growth rate of plr15 was not significantly affected in medium containing pellicin, indeed the growth rate was identical to that of wild type cultures grown in medium lacking pellicin (Supplemental Figure 2). However, the final cell density of wild type grown in medium containing pellicin was significantly higher (OD600=1.242 ±0.06) compared to the final cell density in medium lacking pellicin (OD600=1.006 ±0.06). Based on this observation, the mutation in plr15 does not affect growth rate, but the higher final cell density observed only in the pellicin-treated wild type cultures suggests a connection between cell density and crystalline cellulose production.

The plr15 mutation maps to the catalytic cellulose synthase gene, bcsA

In order to identify the causative mutation conferring pellicin-resistance in plr15, we sequenced the bcs operons from wild type and plr15 genomic DNA. DNA sequence comparisons of the bcs operon genes, revealed a single point mutation in the catalytic cellulose synthase gene, bcsA, of plr15, at position 1345 where a guanine is substituted to adenine. This base mutation is predicted to cause a change from a non-polar alanine residue (A) to a polar threonine residue (T) at position 449 of the amino acid sequence (A449T). No other mutations were found in the remaining plr15 bcs operon gene sequences.

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To confirm that the A449T missense mutation in BcsA was indeed the causative mutation for the observed pellicin resistance, the mutation was recreated in wild-type DNA by site-directed mutagenesis. Allele replacement of this mutated version of bcsA (bcsa^A449T) was achieved through homologous recombination in wild type cells using a modified version of the vector pKNG101 (31). The pKNG101 plasmid has the advantage of having a streptomycin-resistance gene as a selectable marker for the cointegration event as well as the Bacillus subtilis sacB gene as a counter-selectable marker to improve a second crossover event (31). The sacB gene encodes a levansucrase enzyme which in several genera of gram-negative bacteria has been shown to be lethal in the presence of 5% sucrose (31). This property facilitated selection for the integration of the mutated bcsA gene into the chromosome and for the excision of the vector.

Transformation of bacteria with pKNG101 bcsA^A449T ColE1 ori resulted in the appearance of streptomycin-resistant transformants (Sm^R) from the first recombination event. A total of 30 independent Sm^Rtransformants were grown in SH medium without antibiotic. Diluted cultures obtained from these Sm^R transformants were then plated on SH medium supplemented with 5% sucrose. A total of 400 sucrose-tolerant colonies were grown in 200 µL SH medium containing 30 µM pellicin. Of these, eight were able to produce a pellicle in the presence of pellicin. The sequence of the bcsA DNA from three of these colonies revealed a substitution of nucleotide G to A at position 1345 of the gene. This base mutation replicated the one identified in plr15. DNA sequence analysis of the other five pellicle-producing colonies revealed a substitution of nucleotide C to T at position 1346 of the nucleotide sequence of the bcsA gene. This base substitution is predicted to change the alanine residue (A) to a valine residue (V). It is likely that this mutation was the result of a polymerase error during the PCR. Although not originally planned, the generation of this mutant provides additional confirmation that this specific alanine is important for pellicin resistance. Sequencing of bcsA DNA from 10 colonies that did not produce a pellicle in the presence of pellicin revealed no nucleotide changes. The pellicin-resistant phenotype observed in both bcsA^A449T and bcsA^A449V mutants suggest that the A449 residue is responsible for the observed difference in pellicin sensitivity.

We confirmed that the newly generated mutants phenocopied the original mutant by growing them in broth cultures in the presence and the absence of pellicin. The newly created bcsA^A449T and bcsA^A449V mutants displayed identical pellicle-forming capacity to the original plr15 mutant (Supplemental Figure 3a). Interestingly, when grown in medium containing high concentrations of pellicin (50 or 100 µM), plr15 and bcsA^A449T formed pellicle more slowly than bcsA^A449V(Supplemental Figure 3b and c). However, plr15 as well as the bcsA^A449T and bcsA^A449V mutants eventually (after 10 days) formed thick pellicles comparable to those formed at a lower pellicin concentration.

The appearance of the pellicles under high magnification using scanning electron microscopy (SEM) indicate that in contrast to wild type cells (Figure 1a and b), mutant pellicles produced in the presence of pellicin (Figure 1d, f, h) contain long cellulose strands that are indistinguishable from those produced in the absence of pellicin (Figure 1c, e, g). Similarly, bcsA^A449Tand bcsA^A449V produced less but significant amounts of crystalline cellulose (approximately 25% less) in the presence of pellicin, indicating that the mutations had comparable effects on cellulose production to plr15 (Figure 2).

To better understand how the missense mutations might affect BcsA function, we mapped the position of the mutations onto a three dimensional model of KxBcsA based on the crystal structure of Rhodobacter sphaeroides BcsA (10). According to the 3D model, the substituted 449 alanine is predicted to be in the middle of the sixth transmembrane helix of the protein (Figure 3). At this position, the alanine residue is predicted to be in close proximity to the translocating glucan as part of the narrow channel accommodating the nascent glucan chain.

Figure 1: Scanning electron micrographs of pellicles from wild-type (WT), plr15, bcsaA449T, or bcsaA449V cultures grown for seven days under static conditions in the absence (a, c, e, and g) or presence of 10 µM pellicin (b, d, f, and h). In contrast to wild type cells which produce no pellicle in the presence of pellicin and are embedded in a gel-like substance (b), pellicles produced by mutant cells are surrounded by long cellulose fibrils (c, d, e, f, g, and h). Bars correspond to 2.5 µm.

Figure 2. Crystalline cellulose formed by wild type, plr15, bcsA^A449T, and bcsA^A449V. The crystalline cellulose content of pellicles from wild type (WT), plr15, bcsA^A449T, and bcsA^A449V mutants in SH (gray bars) or SH+pellicin (white bars) determined by the method described by Updegraff (30). The crystalline cellulose is expressed as glucose equivalents per dry weight (µg/mg). Values are the mean ± standard deviation of three biological replicates. Asterisks indicate statistically significant differences between pellicin-treated and pellicin-untreated cultures according to one-way ANOVA (p<0.05).

Figure 3. Architecture of the K. xylinus BcsA protein modeled after the Rhodobacter sphaeroides cellulose synthase template PDB 4hg6A. The location of alanine at position 449 is indicated by the white spheres and nascent glucan chain is shown in red. The model is coloured based on rainbow colouring scheme with the N-terminus coloured blue and C-terminus coloured red. Each image is rotated 90° relative to the preceding image.

plr mutations affect cellulose synthesis rates

To determine whether plr mutations had any consequences on cellulose synthase activity, crude membrane preparations from wild-type and mutant cultures were used to assay the in vitro rates of ³[H]-UDP-glucose incorporation into cellulose. The mutants exhibited a significant increase (almost double) in the cellulose synthesis rates compared to wild type. (Figure 4). The incorporation of UDP-glucose measured in a standard assay represents both crystalline and none crystalline cellulose. When the assay products were treated with an acetic/nitric acid mixture instead of 0.5 M NaOH, the incorporation rates were low and comparable to those of wild-type, indicating that most of the product measured using standard assay conditions is non-crystalline cellulose (Figure 4). In order to determine if plr mutants produce more or less crystalline cellulose, we measured ¹⁴[C]-glucose incorporation into the cellulose of whole cells grown under static conditions over a longer time frame (5 hours). In contrast to the first assay, plr mutant cultures produce significantly less crystalline cellulose than wild-type cultures (Figure 5). Taken together, these results suggest that the higher rates of cellulose synthesis are the result of a reduction in cellulose crystallinity rather than a more direct consequence of altered catalytic activity of the enzyme, BcsA. Since these effects are in contrast to the crystalline cellulose measurements obtained using dried pellicles as described above, we also measured cellulose crystallinity by powder X-ray diffraction (XRD) to determine if the reduced cellulose crystallinity was a feature of hydrated cellulose. Cellulose crystallinity indices of plr pellicles obtained by XRD were comparable to untreated, wild type pellicles (Figure 6), indicating that dried pellicles contain crystalline cellulose I.

Figure 4. In vitro cellulose synthase assay using membrane preparations of wildtype and plr mutant cells with UDP-[³H]glucose as substrate. Mutants show an increased cellulose synthase activity. Reactions treated with 0.5 M NaOH (NaOH) contain both cellulose I and cellulose II. Acetic-nitric acid (Acid) treatment of reactions removes cellulose II while retaining cellulose I. Values are the mean ± standard of three experimental determinations. Letters indicate statistically significant differences compared to wild type (a) or compared to plr15 and bcsA^A449T (b) according to two-tailed student t-test (p<0.05).

Figure 5. Comparison of radiolabeled glucose incorporation into the cellulose fraction of pellicles from wild type and plr mutants. The mutants exhibit reduced radiolabeled glucose incorporation into the acid-insoluble fraction compared to the wild type. Measurements were determined after bacterial cultures were incubated in ¹⁴C-glucose for five hours. The vertical axis is expressed as percentage of ¹⁴C-glucose detected in the insoluble fractions divided by the soluble plus insoluble fractions. Asterisks indicate statistically significant differences compared to wild type according to two-tailed student t-test (p<0.05).

Values are the mean ± standard deviation (n=6).

Figure 6. Relative crystallinity index (RCI) of extracellular cellulose produced by culturesgrown in the absence (grey) or presence of 10 μM pellicin (white) based on powder X-ray diffraction. Asterisk indicates statistically significant difference compared to wild type according to two-tailed student t-test (p<0.05). Values are the mean ± SD (n=3).

Cellulose biosynthesis in K. xylinus is a complex, poorly understood process involving an assemblage of proteins (32,33). In an effort to create additional tools for elucidating this process, we had conducted a chemical genetics screen to identify molecules that impinge on the production of crystalline cellulose in K. xylinus, which resulted in the identification of the cellulose biosynthesis inhibitor, pellicin (29). In the present study, we have gained insights into the mode of action of this molecule by isolating mutations that confer resistance to its inhibitory effect on cellulose pellicle formation. The pellicin-resistant mutations lead to the production of comparable amounts of crystalline cellulose when cultures were grown in the absence of pellicin and about 80% of the wild type levels of crystalline cellulose when pellicin was present in the growth medium.

Cloning the causative mutation of the pellicin-resistant mutant, plr15, revealed that an A449T substitution in the BscA protein was involved in pellicin resistance. This was confirmed by site-directed mutagenesis which recreated the same mutation in wild type cells. During the course of generating the A449T mutation, we also identified mutants with an A449V substitution, which resulted in mutants that are phenotypically similar to those with the threonine substitution. In this regard, the A449T mutation resulted in a non-polar to polar substitution and the A449V mutation in a non-polar to a non-polar substitution; therefore, it seems that the polarity of the substitution at the A449 position of BcsA is not the determining factor for conferring pellicin resistance, rather it is more likely a result of the bulkier side chain of valine compared to the wild type alanine.

In order to localize the alanine 449 residue in BcsA, we mapped the A449 position onto a 3D model of the BscA protein. Alignment with the BcsA protein from Rhodobacter sphaeroides revealed that the alanine 449 residue maps to the sixth transmembrane domain (TMH6) of the protein. TMH6 of BcsA forms part of the transmembrane pore which allows the translocation of the nascent glucan chain from the plasma membrane into the periplasm (10). It has been shown that molecules that disrupt cellulose crystallization, such as calcofluor and pellicin, also cause an increase in the rate of glucose polymerization indicating that polymerization and crystallization are coupled processes (29,34,35). Interestingly, calcofluor-induced non-crystalline cellulose is only observed in the wet state and reverts to crystalline cellulose I in the dried state (35). Interpretation of this result is that calcofluor disrupts microfibril assembly in the wet state which is reversed as the hydrogen bonds between the glucan chains form upon drying (35). These observations are supported by the crystal structures of BcsA-BcsB from R. sphaeroides which predict that glucan chain extension and translocation are coupled (10,33). This implies that the rate of polymerization is limited by the time necessary for emerging glucan chains to hydrogen bond as well as by glucan translocation. In agreement with these observations, the consequences of missense plr mutations at A449 confer not only resistance to pellicin, but also cause an increase in the rate of glucose polymerization further implying that the cellulose is less crystalline. Furthermore, at least in the short term, the mutations also cause a decrease in the amount of glucose that is incorporated into crystalline cellulose. In dried plr-derived pellicles, however, the total amount of crystalline cellulose is comparable to that of wild-type.

In K. xylinus, altering the interactions between amino acids of TMH6 in plr mutants and the translocating glucan may change the configuration of the nascent chain prior to crystalline microfibril assembly. This may in turn, cause collateral effects in crystalline cellulose production. Another way in which altering the translocation process may disrupt cellulose crystallization involves the geometry of the glucan chain as it is extruded from the BscA-BscB complex. In particular, the glucan exits the complex between loops 5/6 and 7/8 at the BcsA-BcsB interface, towards the periplasm, twisting so that it protrudes laterally from the complex (10). The precise extrusion microenvironment could be indispensable for the proper interaction between the nascent glucan and other proteins in the periplasm required for cellulose crystallization. Therefore, if pellicin were able to alter the ability of an accessory protein to interact with the TM region of BcsA, it could also affect glucan extrusion thereby hindering the overall crystallization process.

By analogy to the plant Arabidopsis, Harris et al. (36) have shown that resistance to the cellulose biosynthesis inhibitor, quinoxyphen, is the result of mutations in the bcsA-homologous gene, CESA1. Interestingly, a missense mutation in CESA1 causing an A903V substitution leads to quinoxyphen resistance as well as reduced crystalline cellulose content and crystallite size (36). In addition, the velocity of cellulose synthase complex movement across the plasma membrane is increased in the mutant, suggesting an increase in the rate of polymerization (36). The cesa1^A903Vmutation aligns with the tyrosine 455 residue of BcsA in R. sphaeroides which likely interacts with the translocating glucan (10). In K. xylinus, the latter residue aligns in the TMH6 with a histidine 445 residue, which is positionally upstream of the alanine 449 residue. The A449 substitutions have similar effects to the A-V substitution observed in the Arabidopsis orthologue, therefore, it is plausible that pellicin disrupts cellulose synthesis in a similar manner to quinoxyphen, by indirectly disrupting glucan chain translocation. Overall, this implies that the process of glucan translocation in both domains is a general feature of cellulose synthesis and can have a profound effect on crystalline cellulose production.

Bacteria, medium and growth conditions

All strains of Komagataeibacter xylinus (ATCC 53582) were cultured in liquid or on solid Schramm-Hestrin (SH)/agar medium at 30°C. For preparations requiring cells free of cellulose, 0.3% (v/v) cellulase from Trichoderma reesei ATCC 26921 (Sigma-Aldrich) was added to the culture medium 24 h before harvesting to digest the cellulose and obtain a uniform suspension. E. coli strains used in this study (DH5α, 5-alpha F’ Iq, and Mach1 pir116+), were grown in Luria-Bertani (LB) broth at 37°C under static conditions or on a rotatory shaker (250 rpm). For selection of resistant markers, antibiotics were used at the following concentrations: kanamycin, 50 µg/mL; ampicillin, 100 µg/mL; and streptomycin, 50 µg/mL. The E. coli strain Mach1 pir116+ was kindly provided by Dr. Ayush Kumar (University of Manitoba), whereas DH5α, 5-α F’ Iq, and dam−/dcm− strains were from New England Biolabs.

EMS mutagenesis and mutant isolation

Wild type cells were mutagenized by treating 3.2 x 10⁷cells/ml with 140 mM ethyl methane sulfonate (EMS) for 50 min at 30°C. This resulted in survival of ~1.6 x 10⁷cells/ml. Approximately 4 million mutagenized cells were used to seed four 96-well plates with 0.2 mL SH containing 10 µM pellicin. The wells were monitored for the presence of a pellicle after 5 days incubation at 30°C under static conditions. Pellicles that formed were collected and digested with cellulase, diluted and used to inoculate another four sets of 96-well plates. This was repeated one more time and pellicle forming cells were diluted and spread-plated on solid medium containing 10 µM pellicin to isolate individual colonies that were resistant to pellicin. In total, 18 isolates that showed consistent pellicin resistance were retained for further analysis.

Preparation of cultures to determine the degree of pellicin resistance

Cells from a single colony were first cultivated in SH liquid medium on a rotary shaker at 30°C for 7 days. A cellulose-free uniform suspension cells was obtained by adding cellulase to the growth medium at a final concentration of 0.3% (v/v). The initial inoculum was prepared as described above. The presence or absence of a pellicle was assessed after 7 days under static conditions at 30°C. Each well of a 96-well plate was loaded with a total volume of 200 µL of bacterial culture containing either dimethylsulfoxide (DMSO) or pellicin dissolved in DMSO; pellicin concentrations ranged from 5 to 200 µM. The results are representative of nine technical replicates obtained from three biological replicates.

Growth kinetics of wild-type and plr cultures

In order to determine the effect of pellicin on the growth of K. xylinus wild type and the plr15 mutant, cultures were examined in SH medium containing or lacking 10 µM pellicin. Growth kinetic data was collected from cultures grown in 96-well microtitre plates inoculated with a total volume of 200 µL SH medium containing 0.3% (v/v) cellulase and either DMSO or pellicin dissolved in DMSO. The inoculum was prepared by harvesting 5-day old, cellulase-digested cultures by centrifugation at 17,000 x g for 5 minutes at room temperature, followed by three washes with fresh SH medium. The starting inoculum was adjusted to an optical density at 600 nm (OD600) of 0.02 in SH broth. The bacterial culture plates were incubated at 30°C with shaking at 150 rpm. The optical density was measured using Bio-Rad xMark^TM Microplate Absorbance Spectrophotometer (Bio-Rad Laboratories Ltd., Mississauga, ON). Bacterial growth was monitored for 154 hours. The data from eight technical replicates obtained from two biological replicates were averaged and used for statistical analysis.

Determination of crystalline cellulose content

The crystalline cellulose from pellicles formed by plr mutants and wild type was determined as previously described (30). Briefly, inocula from plr15 and wild type were prepared as described above. Pellicles from 7 day-old cultures were harvested and washed with acetone five times and air-dried at room temperature for 10 days. The dried pellicles were weighed and 15 mg of each pellicle transferred to a glass test tube. Each pellicle fraction was soaked in 3 mL of Updegraff solution (1:2:8 acetic acid:water:nitric acid) in a boiling water bath for 1 h. The acid resistant pellicles were transferred to pre-weighed Whatman GF/A glass fibre filters and washed several times with 70% ethanol by vacuum. These insoluble cellulose fractions were then allowed to dry overnight at room temperature. The pellicles and glass fibre filters were placed in 6-well plates and 5 mL of 67% (v/v) sulfuric acid was added to each well on a rotatory shaker at room temperature to completely hydrolyze the cellulose. The total crystalline cellulose content in each pellicle fraction was estimated as glucose equivalents using an anthrone assay (30).

DNA manipulations

DNA isolation from K. xylinus cultures was carried out using a modified protocol based on Murray and Thompson (37). Briefly cells from a 50 mL bacterial culture were harvested by centrifugation and lysed with 500 µL of 2X cetyl trimethyl ammonium bromide (CTAB) buffer (2% (w/v), 1.4 M NaCl, 100 mM Tris-HCl pH 8.0, and 20 mM EDTA) containing 50 µg (w/v) RNaseA for 30 min at 65°C. The lysed cells were cooled to room temperature then an equal volume of chloroform was added and the contents were mixed by inversion. The solution was centrifuged for 10 minutes at 17,000 x g to separate the aqueous and organic phases. The upper aqueous phase was transferred to a fresh tube and mixed with an equal volume of 2-propanol, then centrifuged for 20 minutes at 7,000 x g to pellet the DNA. The pellet was washed with 70% ethanol by centrifugation at 7,000 x g for 5 minutes. The ethanol layer was removed and the pellet was air dried for 15 minutes. Finally, the pellet was re-suspended in 100 µL of TE buffer (10 mM Tris HCl pH 8.0, 1 mM EDTA).

The bcs operon genes bcsA, bcsB, bcsC, and bcsD from wild type and plr15 cultures were amplified using a touchdown PCR protocol using oligonucleotide primers designed according to the published cellulose synthase operon sequence of K. xylinus ATCC 53582 (GenBank accession number X54676.1). The parameters for touchdown PCR were: 98°C for 2 minutes, followed by 10 cycles of 98°C for 30s, 60°C (decreasing by 1°C/cycle) for 30s, and 72°C for 3 minutes; followed by 30 cycles of 98°C for 10s, 56°C for 30s, and 72°C for 3 minutes with a final extension at 72°C for 5 minutes. Primer pairs used for amplification and DNA sequencing are listed in Supplemental Table 2.

Site-directed mutagenesis and allele replacement

The bcsA gene was PCR-amplified with high fidelity Phusion polymerase (New England Biolabs) using wild type genomic DNA as template. The PCR primers used for this amplification were BcsA BamHI Frwd (5’- TACGGATCCAACGAAGAAGAATCCTAAGGC-3’) and BcsA SpeI Rev (5’-ATCACTAGTGACGGGTTGTTCGTATCGT-3’). These primers introduced a 5’ BamHI site and a 3’ SpeI site on the ends of the PCR product. PCR conditions for this amplification were: 98°C for 2 minutes, followed by 10 cycles of 98°C for 30 s, 60°C (decreasing by 1°C/cycle) for 45 s, 72°C for 2 minutes and 30 s, followed by 30 cycles 98°C for 10 s, 56°C for 45 s, and 72°C for 2 minutes and 30 s with a final extension at 72°C for 5 minutes.

The bcsA PCR fragment was subsequently blunt-end cloned into the EcoRV site of pZErO-2 (Invitrogen). The resulting plasmid, named pZErO-2 bcsA, was sequenced to confirm the correct sequence of the bcsA gene was present. The bcsA fragment was then subcloned using the engineered BamHI and SpeI sites into the suicide plasmid vector pKNG101, which was later used for allele replacement. The new plasmid, pKNG101 bcsA ColE1 ori, contained the ColE1 origin of replication from pZErO-2 in addition to the endogenous R6K ori origins of replication; neither origin of replication allows for plasmid replication in K. xylinus. The plasmid sequence was confirmed by sequencing (Supplemental Figure 4).

Site directed mutagenesis of the bcsA gene was performed by substituting the GCC codon at position 1345 of the coding sequence corresponding to A449 with ACC, which codes for threonine. This was done using the forward primer BcsA Ala1345Thr Fwrd (5’ CATGTTCCACACCGTCGGCACG-3’) and reverse primer BcsA Ala1345Thr Rev (5’-TGCGGGATGGCATAGGCC-3’). The PCR reaction conditions were: 98°C for 2 minutes, followed by 25 cycles of 98°C for 30s, 60°C for 45s, and 72°C for 2.5 minutes and a final extension at 72°C for 5 minutes. A 10X Kinase-Ligase-DpnI Mix (10X KLD) was then used for phosphorylation, intramolecular circularization of the PCR product, and removal of the template as per manufacturer's directions (New England Biolabs). The construct was transformed using high-efficiency DH5α competent cells. The presence of the mutation was confirmed by DNA sequencing.

Transformation of K. xylinus with pKNG101 bcsA ColE1 ori resulted in the appearance of streptomycin-resistant transformants (Sm^R) from the first homologous recombination. A total of 30 independent streptomycin-resistant transformants obtained from electroporation of K. xylinus wild type cells with the pKNG101 bcsA ColE1 ori construct were grown in SH medium with shaking (150 rpm) at 30°C overnight. A volume of 150 µL of diluted cultures was plated on SH medium supplemented with 5% sucrose. A total of 400 sucrose-tolerant colonies were then grown in 200 µL SH medium containing 30 µM pellicin. A total of 8 pellicle-positive clones were obtained using this procedure. Genomic DNA from pellicle-positive and pellicle-negative colonies was extracted using the CTAB method described above. DNA sequencing of PCR products generated from both positive and negative clone genomic DNA was used to confirm the presence or absence of the site-directed mutation in the bcsA gene.

Scanning electron microscopy

Pellicles were prepared for electron microscopy as previously described (29). Observations were made using a Hitachi FlexSEM 1000 scanning electron microscope.

In vitro cellulose synthase assays and ¹⁴[C]-glucose incorporation into cellulose

Cellulose synthase assays using crude membrane preparations were performed as previously described (29). Radioactive ¹⁴[C]-glucose incorporation into cellulose of K. xylinus cultures were carried out by inoculating 1 mL of SH medium containing 1% glucose with cells to an OD₆₀₀ = 0.5. Cultures were incubated for 2 h at 30°C under static conditions, followed by addition of 5 µCi of ¹⁴[C]-glucose and incubated for an additional 5 h under the same conditions. Cells were harvested by centrifugation and washed 3 times with 1 mL fresh SH medium. To each pellet, 1 mL Updegraff solution (30) and incubated in a boiling water bath for 1 h. Insoluble material was collected onto Whatman GF/A glass fibre filters and the flow-through collected in fresh tubes. Filters were then washed 3 times with 4 mL water and once with 4 mL methanol. Filters were allowed to dry overnight at room temperature. The total activity of soluble and insoluble material was determined using a liquid scintillation counter.

Statistical analysis.

All statistics were performed using SigmaPlot 12.5 software. A student’s t-test or a one-way ANOVA test were performed for statistical analysis, and values were determined to be significant at a P value of < 0.05. A Saphiro-Wilk test was run in parallel to the one-way ANOVA test with P values for normality and equal variance set up at 0.050 in order to determine homogeneity of variance.

Protein modelling.

Structural analysis of K. xylinus BcsA was performed using the Phyre2 Protein Fold Recognition Server (39) based on the Rhodobacter sphaeroides cellulose synthase template PDB 4hg6A, to model a cellulose translocation intermediate of cellulose synthase subunit A. The pdb files created from these models were visualized using PyMOL software (40).

Powder X-ray Diffraction

Sample preparation for X-ray diffraction (XRD) to assess the crystallinity of cellulose was as previously described (29). X-ray diffractograms were recorded with a Philips PW3710 with Cu Ka radiation (1.54060 Å) with the generator working at 10kV and 10 mA. Angular scanning was at a 2  step size of 0.020, a step time of 2.5 s. The relative crystallinity index (RCI) was calculated according to Segal et al. (41) using the formula RCI = (I_t-I_a/I_t) x 100, where I_t is the total intensity of the (110) peak for cellulose I at 22.73° 2 22 and, for wild type culture with pellicin, of the (020) peak for cellulose II at 21.73° 2. TheI_a is the amorphous intensity at 18° 2 for cellulose I and 16° 2 for cellulose II (Supplemental Figure 5a). Peak identity was confirmed by comparison to diffraction patterns of cellulose I (42) using Match! Software (Crystal Impact, Germany).

Ethics approval and consent to participate

Not applicable

Consent for publication

Not applicable

Availability of data and materials

All data generated or analysed during this study are included in this published article and its supplementary information files.

Competing interests

The authors declare that they have no competing interests.

Funding

The study was supported by funding from the Natural Science and Engineering Council of Canada.

Authors’ contributions

SB conducted the forward genetic screen. REAME analyzed pellicles using SEM. LS conducted all other experiments and contributed to the writing of the manuscript. DB and JS designed the experiments and wrote the manuscript. All authors read and approved the final manuscript.

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Missense mutations in a transmembrane domain of the Komagataeibacter xylinus BcsA lead to changes in cellulose synthesis

Status:

Journal Publication

Version 1

Abstract

Figures

Full text

Background

Results

Forward genetic screening identifies mutant with resistance to pellicin

The plr15 mutation maps to the catalytic cellulose synthase gene, bcsA

plr mutations affect cellulose synthesis rates

Discussion

Materials and Methods

Bacteria, medium and growth conditions

EMS mutagenesis and mutant isolation

Preparation of cultures to determine the degree of pellicin resistance

Growth kinetics of wild-type and plr cultures

Determination of crystalline cellulose content

DNA manipulations

Site-directed mutagenesis and allele replacement

Scanning electron microscopy

In vitro cellulose synthase assays and ¹⁴[C]-glucose incorporation into cellulose

Statistical analysis.

Protein modelling.

Powder X-ray Diffraction

Declarations

Ethics approval and consent to participate

Consent for publication

Availability of data and materials

Competing interests

Funding

Authors’ contributions

References

Supplementary Files

Status:

Journal Publication

Version 1

Missense mutations in a transmembrane domain of the Komagataeibacter xylinus BcsA lead to changes in cellulose synthesis

Status:

Journal Publication

Version 1

Abstract

Figures

Full text

Background

Results

Forward genetic screening identifies mutant with resistance to pellicin

The plr15 mutation maps to the catalytic cellulose synthase gene, bcsA

plr mutations affect cellulose synthesis rates

Discussion

Materials and Methods

Bacteria, medium and growth conditions

EMS mutagenesis and mutant isolation

Preparation of cultures to determine the degree of pellicin resistance

Growth kinetics of wild-type and plr cultures

Determination of crystalline cellulose content

DNA manipulations

Site-directed mutagenesis and allele replacement

Scanning electron microscopy

In vitro cellulose synthase assays and 14[C]-glucose incorporation into cellulose

Statistical analysis.

Protein modelling.

Powder X-ray Diffraction

Declarations

Ethics approval and consent to participate

Consent for publication

Availability of data and materials

Competing interests

Funding

Authors’ contributions

References

Supplementary Files

Status:

Journal Publication

Version 1

In vitro cellulose synthase assays and ¹⁴[C]-glucose incorporation into cellulose