Improved growth rate in Clostridium thermocellum hydrogenase mutant via perturbed sulfur metabolism

Background Metabolic engineering is a commonly used approach to develop organisms for an industrial function, but engineering aimed at improving one phenotype can negatively impact other phenotypes. This lack of robustness can prove problematic. Cellulolytic bacterium Clostridium thermocellum is able to rapidly ferment cellulose to ethanol and other products. Recently, genes involved in H2 production, including the hydrogenase maturase hydG and NiFe hydrogenase ech, were deleted from the chromosome of C. thermocellum. While ethanol yield increased, the growth rate of ΔhydG decreased substantially compared to wild type.ResultsAddition of 5 mM acetate to the growth medium improved the growth rate in C. thermocellum ∆hydG, whereas wild type remained unaffected. Transcriptomic analysis of the wild type showed essentially no response to the addition of acetate. However, in C. thermocellum ΔhydG, 204 and 56 genes were significantly differentially regulated relative to wild type in the absence and presence of acetate, respectively. Genes, Clo1313_0108-0125, which are predicted to encode a sulfate transport system and sulfate assimilatory pathway, were drastically upregulated in C. thermocellum ΔhydG in the presence of added acetate. A similar pattern was seen with proteomics. Further physiological characterization demonstrated an increase in sulfide synthesis and elimination of cysteine consumption in C. thermocellum ΔhydG. Clostridium thermocellum ΔhydGΔech had a higher growth rate than ΔhydG in the absence of added acetate, and a similar but less pronounced transcriptional and physiological effect was seen in this strain upon addition of acetate.ConclusionsSulfur metabolism is perturbed in C. thermocellum ΔhydG strains, likely to increase flux through sulfate reduction to act either as an electron sink to balance redox reactions or to offset an unknown deficiency in sulfur assimilation.

[1]  Richard Sparling,et al.  End-product induced metabolic shifts in Clostridium thermocellum ATCC 27405 , 2011, Applied Microbiology and Biotechnology.

[2]  A. Guss,et al.  Elimination of metabolic pathways to all traditional fermentation products increases ethanol yields in Clostridium thermocellum. , 2015, Metabolic engineering.

[3]  J M Thevelein,et al.  The two isoenzymes for yeast NAD+‐dependent glycerol 3‐phosphate dehydrogenase encoded by GPD1 and GPD2 have distinct roles in osmoadaptation and redox regulation , 1997, The EMBO journal.

[4]  Laura R. Jarboe,et al.  Furfural Inhibits Growth by Limiting Sulfur Assimilation in Ethanologenic Escherichia coli Strain LY180 , 2009, Applied and Environmental Microbiology.

[5]  Lee R. Lynd,et al.  Increase in Ethanol Yield via Elimination of Lactate Production in an Ethanol-Tolerant Mutant of Clostridium thermocellum , 2014, PloS one.

[6]  Lee R. Lynd,et al.  Identifying promoters for gene expression in Clostridium thermocellum , 2015, Metabolic engineering communications.

[7]  M. Teixeira,et al.  Characterization of the Desulfovibrio desulfuricans ATCC 27774 DsrMKJOP complex--a membrane-bound redox complex involved in the sulfate respiratory pathway. , 2006, Biochemistry.

[8]  I. S. Pretorius,et al.  Microbial Cellulose Utilization: Fundamentals and Biotechnology , 2002, Microbiology and Molecular Biology Reviews.

[9]  Cong T. Trinh,et al.  Elucidating central metabolic redox obstacles hindering ethanol production in Clostridium thermocellum. , 2015, Metabolic engineering.

[10]  Harald Huber,et al.  Proteomic Characterization of Cellular and Molecular Processes that Enable the Nanoarchaeum equitans-Ignicoccus hospitalis Relationship , 2011, PloS one.

[11]  L. Lynd,et al.  Deletion of nfnAB in Thermoanaerobacterium saccharolyticum and Its Effect on Metabolism , 2015, Journal of bacteriology.

[12]  Lee R Lynd,et al.  Closing the carbon balance for fermentation by Clostridium thermocellum (ATCC 27405). , 2012, Bioresource technology.

[13]  Jonathan R. Mielenz,et al.  Mutant selection and phenotypic and genetic characterization of ethanol-tolerant strains of Clostridium thermocellum , 2011, Applied Microbiology and Biotechnology.

[14]  Lee R Lynd,et al.  Redirecting carbon flux through exogenous pyruvate kinase to achieve high ethanol yields in Clostridium thermocellum. , 2013, Metabolic engineering.

[15]  M. Taillefer,et al.  Reassessment of the Transhydrogenase/Malate Shunt Pathway in Clostridium thermocellum ATCC 27405 through Kinetic Characterization of Malic Enzyme and Malate Dehydrogenase , 2015, Applied and Environmental Microbiology.

[16]  Oriol Gutierrez,et al.  Simultaneous online measurement of sulfide and nitrate in sewers for nitrate dosage optimisation. , 2010, Water science and technology : a journal of the International Association on Water Pollution Research.

[17]  Chunaram Choudhary,et al.  Acetyl-phosphate is a critical determinant of lysine acetylation in E. coli. , 2013, Molecular cell.

[18]  J. Wall,et al.  Genetics and Molecular Biology of the Electron Flow for Sulfate Respiration in Desulfovibrio , 2011, Front. Microbio..

[19]  V. Müller,et al.  Biochemistry, evolution and physiological function of the Rnf complex, a novel ion-motive electron transport complex in prokaryotes , 2011, Cellular and Molecular Life Sciences.

[20]  L. Lynd,et al.  Elimination of hydrogenase active site assembly blocks H2 production and increases ethanol yield in Clostridium thermocellum , 2015, Biotechnology for Biofuels.

[21]  D. Tabb,et al.  MyriMatch: highly accurate tandem mass spectral peptide identification by multivariate hypergeometric analysis. , 2007, Journal of proteome research.

[22]  L. Lynd,et al.  Elimination of formate production in Clostridium thermocellum , 2015, Journal of Industrial Microbiology & Biotechnology.

[23]  Jie Zhang,et al.  A Targetron System for Gene Targeting in Thermophiles and Its Application in Clostridium thermocellum , 2013, PloS one.

[24]  Shihui Yang,et al.  Clostridium thermocellum ATCC27405 transcriptomic, metabolomic and proteomic profiles after ethanol stress , 2012, BMC Genomics.

[25]  Lee R Lynd,et al.  Transformation of Clostridium thermocellum by electroporation. , 2012, Methods in enzymology.

[26]  Michael D. Litton,et al.  IDPicker 2.0: Improved protein assembly with high discrimination peptide identification filtering. , 2009, Journal of proteome research.

[27]  L. Lynd,et al.  High Ethanol Titers from Cellulose by Using Metabolically Engineered Thermophilic, Anaerobic Microbes , 2011, Applied and Environmental Microbiology.

[28]  Peyman Ezzati,et al.  Proteomic analysis of Clostridium thermocellum core metabolism: relative protein expression profiles and growth phase-dependent changes in protein expression , 2012, BMC Microbiology.

[29]  Donna M Kridelbaugh,et al.  Nitrogen and sulfur requirements for Clostridium thermocellum and Caldicellulosiruptor bescii on cellulosic substrates in minimal nutrient media. , 2013, Bioresource technology.

[30]  Courtney M. Johnson,et al.  Clostridium thermocellum transcriptomic profiles after exposure to furfural or heat stress , 2013, Biotechnology for Biofuels.

[31]  Venkatesh Balan,et al.  Designer synthetic media for studying microbial-catalyzed biofuel production , 2015, Biotechnology for Biofuels.

[32]  Eric Verdin,et al.  Reversible lysine acetylation controls the activity of the mitochondrial enzyme acetyl-CoA synthetase 2 , 2006, Proceedings of the National Academy of Sciences.

[33]  Lee R. Lynd,et al.  Development of pyrF-Based Genetic System for Targeted Gene Deletion in Clostridium thermocellum and Creation of a pta Mutant , 2010, Applied and Environmental Microbiology.

[34]  Lee R Lynd,et al.  Dcm methylation is detrimental to plasmid transformation in Clostridium thermocellum , 2012, Biotechnology for Biofuels.

[35]  B. Davison,et al.  Clostridium thermocellum DSM 1313 transcriptional responses to redox perturbation , 2015, Biotechnology for Biofuels.

[36]  Daniel Amador-Noguez,et al.  The exometabolome of Clostridium thermocellum reveals overflow metabolism at high cellulose loading , 2014, Biotechnology for Biofuels.

[37]  R. Thauer,et al.  NADP+ Reduction with Reduced Ferredoxin and NADP+ Reduction with NADH Are Coupled via an Electron-Bifurcating Enzyme Complex in Clostridium kluyveri , 2010, Journal of bacteriology.