Abstract

Acetogenic bacteria are capable of fermenting CO2 and carbon monoxide containing waste-gases into a range of platform chemicals and fuels. Despite major advances in genetic engineering and improving these biocatalysts, several important physiological functions remain elusive. Among these is quorum sensing, a bacterial communication mechanism known to coordinate gene expression in response to cell population density. Two putative agr systems have been identified in the genome of Clostridium autoethanogenum suggesting bacterial communication via autoinducing signal molecules. Signal molecule-encoding agrD1 and agrD2 genes were targeted for in-frame deletion. During heterotrophic growth on fructose as a carbon and energy source, single deletions of either gene did not produce an observable phenotype. However, when both genes were simultaneously inactivated, final product concentrations in the double mutant shifted to a 1.5:1 ratio of ethanol:acetate, compared to a 0.2:1 ratio observed in the wild type control, making ethanol the dominant fermentation product. Moreover, CO2 re-assimilation was also notably reduced in both hetero- and autotrophic growth conditions. These findings were supported through comparative proteomics, which showed lower expression of carbon monoxide dehydrogenase, formate dehydrogenase A and hydrogenases in the ∆agrD1∆agrD2 double mutant, but higher levels of putative alcohol and aldehyde dehydrogenases and bacterial micro-compartment proteins. These findings suggest that Agr quorum sensing, and by inference, cell density play a role in carbon resource management and use of the Wood-Ljungdahl pathway as an electron sink.

Highlights

  • Acetogenic bacteria are capable of fermenting ­CO2 and carbon monoxide containing waste-gases into a range of platform chemicals and fuels

  • The Wood-Ljungdahl pathway (WLP) comprises of separate methyl and carbonyl branches that converge to produce a single molecule of acetyl-CoA, whereby the methyl branch delivers a methyl group and the carbonyl branch delivers an enzyme-bound CO molecule which combine with coenzyme A to form acetyl-CoA via acetyl-CoA synthase (ACS). ­H2 provides the required reducing equivalents during lithoautotrophic growth on C­ O2, whereas during CO-based growth, reducing equivalents are derived via CO oxidation through carbon monoxide dehydrogenase (CODH)[23,24]

  • Since no other agrB1 homologue could be identified in the genome, it seems that processing of both AgrD1 and AgrD2 signalling peptides relies on the System 1 encoded AgrB1 (Fig. 1)

Read more

Summary

Introduction

Acetogenic bacteria are capable of fermenting ­CO2 and carbon monoxide containing waste-gases into a range of platform chemicals and fuels. Despite major advances in genetic engineering and improving these biocatalysts, several important physiological functions remain elusive Among these is quorum sensing, a bacterial communication mechanism known to coordinate gene expression in response to cell population density. ­CO2 re-assimilation was notably reduced in both hetero- and autotrophic growth conditions These findings were supported through comparative proteomics, which showed lower expression of carbon monoxide dehydrogenase, formate dehydrogenase A and hydrogenases in the ∆agrD1∆agrD2 double mutant, but higher levels of putative alcohol and aldehyde dehydrogenases and bacterial micro-compartment proteins. Emphasis on understanding the WLP has elucidated much in the way of energy conservation, redox metabolism and carbon ­utilisation[42–45], which has laid out incentives for furthering metabolic efficiency and industrial utility Despite these advances, other significant physiological functions are still not yet fully understood such as cell–cell communication systems. Similar observations have been made in C. autoethanogenum’s close relative, C. ljungdahlii, whose transcriptome during fructose and syngas-based fermentation revealed upregulation of both QS and sporulation associated ­genes[46]

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.