Difference between revisions of "Team:British Columbia/Project/S-Layer/Cellulases"

Abstract

Lignocellulosic biomass, the most abundant renewable resources in nature, represents a promising alternative to fossil fuels for sustainable production of chemicals and material. Plenty of the available lignocellulosic biomass is not a food source for humans and its industrial exploitation does not conflict with agricultural usage. However, the main technological obstacle for industrial exploitation of biomass is the recalcitrant nature of lignocellulosic polymers. One approach to harness the energy contained in biomass is to convert the lignocellulosic polymers in simple sugars, which can be further transformed in valuable compounds, using microorganisms. Some anaerobic microorganisms have developed approaches to break down recalcitrant plant biomass using elaborate extracellular enzyme complexes, containing a scaffolding protein with many attached cellulolytic enzymes. The systems were adopted by scientists to generate artificial cellulosomes. But the assembly of such complexes requires engineering of highly specific cohesin-dockerin interactions.

Our approach focuses on adapting the surface layer of Caulobacter crescentus for the highly efficient display of cellulolytic enzymes. We specifically chose C. crescentus as it natively expresses a two dimensional crystal lattice protein called a surface layer (S-Layer), which can be engineered to work as an enzyme display. Our goals were to embed cellulolytic enzymes into the S-Layer protein to confirm their proper folding and activity. We believe that our approach will simplify the process of "cellulosome" engineering by exploiting the robust secretion and display system of Caulobacter. The developed platform can be easily adapted for the display of different enzymatic activities.

Key Achievements

Introduction

Plant biomass is the most abundant renewable resource on Earth. Usually plant biomass consists of 30-50% of cellulose, 20-40% hemicellulose carbohydrates and 20-35% lignin heteropolymer, which are integrated in each other to form complex carbohydrate structures recalcitrant to degradation. Cellulose represents a linear polymer of glucose molecules connected through β-1,4 glycoside bonds (Fig.1). In nature the degradation of cellulose into soluble sugars often involves several different enzymes, such as exoglucanases, endoglucanases and β-glucosidases, that act in synergy to cleave the bonds.

Figure 1 Molecular structure of cellulose polymer.

We propose to express a mixture of cellulase-degrading enzymes on the surface of the bacteria Caulobacter crescentus,which will work in synergy to increase the rate of cellulose degradation and yield of monosaccharides release.

Caulobacter crescentus is a gram negative non-pathogenic bacterium found in many freshwater and soil environments (Poindexter,J.S. 1981). It displays, on its outer surface, a crystalline protein lattice called a surface layer (S-layer) which is made of multiple repetitions of the same RsaA protein encasing the whole surface of the cell (Fig.2)(Smit, J.1992).

Figure 2 (left) Schematic top view on Caulobacter crescentus surface layer protein hexagonal arrangement (right) Gram negative cell wall structure with the surface layer.

For our project we have used the RsaA fusion protein secretion system designed by the Smit lab at the University of British Columbia. Using the ΔGCSS strain of C.crescentus which has its own wild type RsaA protein knock-out in the host genome, we have aimed to insert genetically engineered RsaA fusion protein plasmids to express functional cellulase enzymes fused into the surface layer protein. The use of fusion proteins expressed on the surface of the cell would allow for the breakdown of cellulase without any diffusion of the substrate in and out of the cell.

Design

Engineering of the S-layer, encoded by the rsaA gene, has been made possible using a C.crescentus genomic rsaA knockout mutant, that can be complemented with a rsaA gene that contains an internal multiple cloning site. Using the multiple cloning site, genes encoding proteins of interest can be cloned in, in-frame, to create a construct that encodes a contiguous protein that contains the S-layer and internal protein of interest.

In order to engineer cellulases onto the S-layer of C. crescentus, some key criteria had to be met for selection of candidate cellulases. This included that the cellulases had to be as small as possible, ideally less that 30 kDa, N- and C-termini within proximity of each other, and characterization in the literature for heterologous expression and activity. Once a candidate cellulase was identified, a BLAST search against the PDB was conducted to find a structure or structural homolog. Based on the structure or PHYRE2 (Protein Homology/analogY Recognition Engine V 2.0) homology modeling, and comparison with construct design in the literature, a construct was designed (Fig 3).

Figure 2 Structures of cellulases candidates.A) Structure of Gluc1C bound to thiocellobiose (purple) (PDB:2O9R_A). The structure includes amino acids 4-448, which is what we chose for our construct design for S-layer expression. N- and C-termini are within close proximity (colored blue and red, respectively). B) Model of CenA structure generated by PHYRE2 using PDB:1UOZ, endoglucanase Cel6 from Mycobacterium tuberculosis, as a structural model. The two sequences share 42% sequence identity and the model includes amino acids 162-447 and thiocellopentose (cyan) superimposed using the substrate bound 1UOZ template structure. Colored in pale blue are amino acid residues 162-189 that were excluded from the construct design for S-layer expression. The CenA construct for S-layer expression included amino acids 190-447 and N- and C-termini are colored blue and red, respectively.

This process was done for all seven candidate cellulases. This meant that the carbohydrate domain was excluded and N-terminal regions were trimmed. Also, one cellulase, E1, constructs were designed to include (E1_422) or exclude (E1_399) the linker region between the cellulase and carbohydrate-binding domain, a P[S,T]-rich repeat region, based on activity described in the literature. Candidate cellulases were codon optimized for expression in C. crescentus and synthesized by IDT.

Methods

All Caulobacter cultures were grown in PYE media supplemented with 2 μg/ml chloramphenicol unless stated otherwise. All plasmid DNA extractions were performed with QIAprep Spin Miniprep Kit (Qiagen). DNA purification from gels or PCR mixtures were done with NucleoSpin® Gel and PCR Clean-up kit(Macherey-Nagel).

Cloning of laccase enzyme into rsaA plasmid in C. crescentus

The synthesized cellulase DNA was amplified using PCR with HF Phusion polymerase in 100 μl reactions.The following primers were used to amplify the selected region of cellulases genes and to add the BglII and PstI or NheI cut sites for cloning in p4A_723 plasmid:

Table 1 Primers for cloning cellulase gene inserts into rsaA P4A723 plasmid.

For the cloning of Endo5A, GlucIC, G12, E1_422 and E1_399 in P4A723 rsaA plasmid, the amplified products and the isolated p4A723 plasmid DNA were digested with BglII and PstI restriction enzymes (NEB). For the cloning of CEX construct, the plasmid and amplified product were digested with BglII and NheI restriction enzymes. The plasmid digests were purified by agarose gel purification, while PCR product digests were purified by PCR purification. Purified digests were ligated using T4 ligase(NEB) and the ligation mixes were then transformed in chemically competent DH5α E. coli. Transformed colonies were then plated on and selected from a LB-CM plate and grown overnight in LB-CM media. Recombinant plasmid was then isolated and sent for Sanger sequencing for confirmation.

After sequence confirmation, the isolated construct DNA were electroporated into electrocompetent C.crescentus with an RsaA Amber mutation and colonies were grown on a PYE-CM plate. After 3 days of growth one colony from each plate was selected and streaked onto a fresh plate, which would be used for all future assays.

Cloning of cellulase enzymes into pSB1C3 plasmid with Ptac promoter and rbs

The synthesized cellulases genes were amplified using PCR with HF Phusion polymerase in 100 μl reactions. The following primers were used to amplify the selected region of cellulases genes and to add BioBrick Prefix and Suffix:

Table 2 Primers for cloning cellulase gene inserts in pSB1C3 plasmid.

Purified pSB1C3 plasmid and the amplified Endo5A, Gluc1C, E1, G12 constructs were digested with EcoRI and SpeI restriction enzymes. The plasmid digests were purified by agarose gel purification, while PCR product digests were purified by PCR purification. Purified digests were ligated using T4 ligase and the ligation mixes were then transformed in chemically competent DH5α E. coli. Transformed colonies were then plated on LB-CM plate and the isolated colonies were selected and grown overnight in LB-CM media. Recombinant plasmid was isolated and sent for Sanger sequencing for confirmation.
pTAC was amplified from Bba_K868400 part using HF phusion PCR with the following primers to add the rbs (part Bba_B0034): Ptac_rbs_F 5'-GTTTCTTCGAATTCGCGGCCGCTTCTAGAgagctgttgacaatta, Ptac_rbs_R 5'-GTTTCTTCCTGCAGCGGCCGCTACTAGTtttctcctctttaattgttatccgctca
The amplified pTAC and rbs part was then digested with EcoRI and SpeI restriction enzymes. pSB1C3 high copy assembly plasmid with the gene insert was digested using EcoRI and XbaI restriction enzymes. The plasmid digest was then purified by agarose gel purification while the pTAC RBS digest was purified by PCR purification. Both purified digest were ligated together using standard ligation protocol and ligation mix was then transformed in chemically competent DH5α E. coli.

Surface layer fusion protein extraction

10 mL tubes of PYE-CM were inoculated with C. crescentus strains carrying the different cellulase-rsaA fusions in p4A723 plasmid as well as a positive control carrying a plasmid with wild type rsaA (P4A723) and a negative control of rsaA knock-out (ΔGCSS). Cultures were grown overnight at 30°C shaker. Cultures were taken out of incubator and optical density at 600 nm was measured. All cultures were then normalized to the lowest OD by diluting the remaining culture with PYE.
Low pH extraction (Walker et al. 1992) was performed using different pHs of HEPES buffer to extract only crystalline s-layer without lysing the cells. The procedure is illustrated on Fig.3. Proteins were then stored in -20°C freezer. Remaining cell pellet was used to prepared a cell lysate by resuspending the pellet in 150 μl of lysis buffer and boiling for 5 minutes.

Figure 3 Schematic presentation of low pH extraction procedure.

Surface layer fusion protein expression confirmation

To confirm expression of surface layer fusion protein SDS-PAGE and western blot analysis were performed on extracted proteins from low pH extraction and on the cell lysates from those samples. SDS-PAGE was done using 8% separating gels. Coomassie Brilliant Blue staining and western immunoblotting was performed using protocols outlined in protocol section. Western blots were probed with primary rabbit anti-RsaA polyclonal antibodies at 1/30,000 dilution. Goat anti-rabbit IgG was used as secondary antibody at 1/50,000 dilution. Fluorophore was detected by Odyssey Infrared Imaging System.

Caulobacter Cellulase Activity Analysis

For cellulase enzyme activity measurement, triplicate 5mL PYE-CM starter cultures of p4A723, E1_399, E1_422, Gluc1C and Endo5A were grown in 10 mL tubes on a rotary shaker at 30°C for 2 days. Cultures were taken out of incubator and OD600 was measured. All cultures were then normalized to the lowest OD 600 nm by diluting the remaining culture with PYE. 1 mL of each sample was taken and resuspended with fresh PYE and spin down 3 times to remove any lysed cell debris that may interfere with cellulase activity results.

A protocol for cellulases activity assay was adopted from Mewis K.(2015) . 150 uL of each culture were aliquoted into a clear 96 well plate(Corning) and 150 μL of assay mix (0.1 mg/ml DNPC in 50 mM pH 5.5 potassium acetate buffer) was added to the each well. OD 400 nm and OD 600 nm was measured every 30 minutes for several hours by a VarioScan plate reader(Thermo). Between measurements the culture was incubating at 30°C. Data was normalized further by dividing the OD400nm measurement by the OD600nm measurement.

Growth of Caulobacter displaying cellulases on cellulose as a sole carbon source

Triplicate 5mL PYE-CM starter cultures of p4A723, E1_399, E1_422, Gluc1C and Endo5A were grown in 10 mL tubes on a rotary shaker at 30°C for 2 days. Cultures were taken out of incubator and OD600 was measured. All cultures were then normalized to the lowest OD600 by diluting the remaining cultures with PYE. 100-fold dilution was used to inoculate the cultures in 200 μL well clear plate containing M2 with 0.2% w/v carboxymethylcellulose(CMC). For the co-cultures, equal-volume inoculations were done to make final dilution of 100. The plate was incubate at 30C in a Tecan platereader and OD600 was read every 30 minutes.

Results

Cloning of cellulase enzymes into rsaA plasmid in C.crescentus

Endo5A, Gluc1C, E1_422, and E1_399 were all successfully cloned into the p4A723 plasmid vector and sequence confirmed by Sanger sequencing. Cloning was attempted on G12 several times, each time the transformation step into DH5α E.coli failed, leading to the assumption that the gene product might be toxic to the cell. As Endo5A, E1_422, and E1_399 are all endoglucanases, we decided to not proceed with any troubleshooting on G12. CEX gene was successfully cloned into DH5α E.coli and sequence confirmed. However after transforming the plasmid into Caulobacter, extreme cell clumping was observed, possibly a result of the CEX fusion into the S-Layer. Due to the phenotype, we did not perform functional characterization of the CEX-rsaA fusion.

Figure 4 Map of rsaA p4A723 plasmid.

Surface layer fusion protein extraction expression confirmation

Low pH extraction was done on Endo5A, Gluc1C, E1_399, and E1_422 RsaA fusion proteins as well as P4A732 RsaA positive control and ΔGCSS negative control. We also prepared a cell lysate from the remaining cell pellet to compare the amount of protein within the cell as opposed to on the surface of the cell. We ran two gels simultaneously staining one with Coomassie Brilliant blue and performing western blot on the other.
Thermo fisher prestained protein ladder was used to compare relative expected sizes of fusion proteins. Expected protein sizes were as followed:

On the coomassie stained gel faint bands corresponding to cellulases-rsaA fusions were observed in low PH extracted proteins. The cell lysate showed large amounts of intracellular proteins with poor differentiation so no conclusions could be made from these.
On the western blot analysis, RsaA fusion proteins were clearly observed at higher molecular weight than wild type RsaA confirming successful expression of cellulases fused to the rsaA on the surface. Nothing was displayed on the negative control showing that no wild type RsaA was produced. The cell lysate results were comparable to the low pH extracted proteins, with visibly more RsaA fusion proteins detectable in the cell lysate as opposed to the low pH extracted proteins. This may be a sign that not all of the fusion protein can get out of the cell and crystalize, likely due to the large size of the fusion protein. The higher visibility of some constructs over others in the low pH extraction, such as with E1_399 vs. Gluc1C, is indicative of higher expression and secretion outside of the cell. The smaller constructs such as E1_399 and Endo5A were seen more clearly on both the coomassie stained gel and the western blot, indicating that the smaller constructs might be easier to transport on the surface. Some fragments of lower molecular weight RsaA protein in the western, this is probably due to cleavage of the RsaA protein during the extraction.

Figure 5 (top) Western Blot. Left to right: Thermofisher ladder, Gluc1C cell lysate, Endo5A cell lysate, E1_399 cell lysate, E1_422 cell lysate, ΔGCSS cell lysate, P4A723 cell lysate, Thermofisher ladder, Gluc1C low pH extracted proteins, Endo5A low pH extracted proteins, E1_399 low pH extracted proteins, E1_422 low pH extracted proteins, ΔGCSS low pH extracted proteins, P4A723 low pH extracted proteins
Figure 6 (bottom) Coomassie Brilliant Blue Stain. Left to right: Thermofisher ladder, Gluc1C cell lysate, Endo5A cell lysate, E1_399 cell lysate, E1_422 cell lysate, ΔGCSS cell lysate, P4A723 cell lysate, Thermofisher ladder, Gluc1C low pH extracted proteins, Endo5A low pH extracted proteins, E1_399 low pH extracted proteins, E1_422 low pH extracted proteins, ΔGCSS low pH extracted proteins, P4A723 low pH extracted proteins

Caulobacter cellulase activity analysis

An initial cellulase activity analysis was run using the protocols described in Method section for a period of 150 minutes. The assay mechanism is explained in Fig. 7. 2,4dinitrophenylcellobiose (DNPC) consists of cellobiose bound to a 2,4dinitrophenol chromophore. If cellulase activity is present, the release of chromophore can be observed and measured at OD400

Figure 7 Assay for cellulase activity with DNPC substrate

This assay was run on the Caulobacter cells expressing Endo5A, Gluc1C, E1_399, and E1_422 RsaA fusions using the wild type RsaA P4A723 protein as a control. From the first time point, cellulase-expressing Caulobacters demonstrated high cellulase activities, with E1_422 and E1_399 showing the highest activity level followed by Endo5A (Figure 8). Gluc1C had lower activity levels closer to that of the control, what can be explained by the glucosidase activity of Gluc1C. The enzyme cleaves a glucose molecule from DNPC first, not cellobiose what does not lead to the release of chromophore. Observation at later time points need to be taken to confirm the Gluc1C activity.

Figure 8 Cellulase activity assay results for Caulobacter displaying cellulases

Caulobacter growth on cellulose

Caulobacter cells expressing wild type RsaA, Endo5A, Gluc1C, E1_399, and E1_422 were grown on carboxymethylcellulose(CMC) as a sole carbon source to confirm the cellulase activities of the displayed enzymes. Endo5A and its co-cultures showed the best growth results on CMC (Fig.9) As Caulobacter has intrinsic β-1,4-glucosidase, the displayed endoglucanase cleaves the cellulose in small disaccharide, which are further transformed by periplasmic glucosidase into glucose to sustain Caulobacter growth. E1_399 also demonstrates growth on cellulose and interestingly when co-cultured with Gluc1C it shows synergistic growth. The results suggest Caulobacter can be successfully used to transform cellulose in simple sugars and confirm that the first part of our consortia works!

Figure 9 Caulobacter growth on CMC over 100 hours

Conclusion

For our project we employed robust expression and display system of Caulobacter S-layer for the generation of whole-cell biocatalysts. Previously, the S-layer was used to display small peptides and proteins. Our results are a first demonstration that Caulobacter can be successfully used for enzymes display. The cellulases enzymes used in the study were pre-selected based on their crystal structures and truncated to reduce the size without changing the catalytic activities. The expression of cellulases on cell surface was confirmed by Western blot and the cellulolytic activity was demonstrated in DNPC assay. Also we confirmed that the engineered Caulobacter strains can breakdown and grow on cellulose substrate.

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