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Sharma, B. D.

Publications and source records attributed to Sharma, B. D..

2 recordsLinked to original sources

Understanding Substrate Transport and Metabolism in Clostridium thermocellum to Improve Biofuel Production

As a cellulolytic specialist microbe, Clostridium thermocellum primarily ferments cellulose and its breakdown products. However, the full breadth of its substrate range remains poorly understood. In this work, we investigated the ability of C. thermocellum to transport and metabolize a diverse range of alternative carbon substrates. We performed tetrazolium dye assays to assess the ability of wild-type (WT) C. thermocellum (strain LL1004) to transport and metabolize 190 different substrates and identified 18 positive hits and 27 false positives. These findings guided the selection of 22 substrates for batch fermentations of WT on 10 g/L alternative substrate plus 1 g/L cellobiose. We identified eight substrates that were either fully or partially consumed (cellobiose, glucose, fructose, sorbitol, arbutin, turanose, pyruvate, glucose-6-phosphate), two that were interconverted (malate, fumarate), seven that may undergo conversion to unidentified fermentation products (xylose, sorbose, tagatose, galactose, mannose, rhamnose, fucose), and five that were not consumed (glycerol, acetate, lactate, propionate, xylitol). Sorbitol and pyruvate, which are more and less reduced than cellobiose, respectively, were selected for further analysis of their effects on redox balance and product formation. Batch fermentations on sorbitol and pyruvate demonstrated that ethanol production in C. thermocellum may be limited in part by the availability of reducing equivalents. Collectively, this work demonstrates the utility of alternative carbon substrates as a tool for perturbing metabolism, redox balance, and fermentation product distributions to further our understanding of the metabolism of anaerobic, thermophilic bacteria such as C. thermocellum for the production of biofuels and biochemicals of interest.

microbiology↗

Metabolic imbalance limits fermentation in microbes engineered for high-titer ethanol production

Microbial strains engineered for high-titer ethanol production achieve lower maximum titers compared to native producers such as Zymomonas mobilis. A central unresolved question is why fermentation ceases before substrate has been exhausted by these strains. Here, we integrate metabolite profiling with thermodynamic analysis to examine this phenomenon in engineered strains of Escherichia coli and Thermoanaerobacterium saccharolyticum and compare them to Z. mobilis, a native ethanol producer. In the engineered strains, fermentation cessation coincided with marked pyruvate accumulation, due to a lack of ability to convert pyruvate to ethanol. This resulted in a local thermodynamic equilibrium at the pyruvate kinase reaction, as determined by Max-Min Driving Force (MDF) analysis. Relaxing constraints on pyruvate and related metabolites restored positive MDF values, implicating thermodynamic limitations as the underlying constraint. By contrast, Z. mobilis maintained a positive thermodynamic driving force throughout fermentation, suggesting that product titer is limited by a different mechanism in this organism. These findings establish a systems-level framework linking metabolite concentrations to pathway thermodynamics and highlight opportunities for improving microbial performance in ethanol and other bioproduction contexts.

systems biology↗