Allopurinol-mediated lignocellulose-derived microbial inhibitor tolerance by Clostridium beijerinckii during acetone–butanol–ethanol (ABE) fermentation

• Published in: Applied microbiology and biotechnology 2015-04, Vol.99 (8), p.3729-3740
• Main Authors: Ujor, Victor, Agu, Chidozie Victor, Gopalan, Venkat, Ezeji, Thaddeus Chukwuemeka
• Format: Article
• Language: English
• Subjects: Acetone; Acetone - metabolism; Acids; Alcohol; allopurinol; Allopurinol - metabolism; Analysis; Anti-Bacterial Agents - toxicity; antibiotics; arabinans; Biodiesel fuels; Bioenergy and Biofuels; Biofuels; Biomass; Biomass energy; Biomedical and Life Sciences; Biosynthesis; Biotechnology; butanol; Butanols - metabolism; Clostridium; Clostridium beijerinckii; Clostridium beijerinckii - drug effects; Clostridium beijerinckii - metabolism; Clostridium botulinum; culture media; Dehydrogenases; Deoxyribonucleic acid; Detoxification; DNA; DNA repair; Drug Tolerance; Ethanol; Ethanol - metabolism; Fermentation; Furaldehyde - toxicity; Furfural; glucans; Glycerol; Growth media; hydrolysates; Hypoxanthine; Influence; Inhibitors; Life Sciences; Lignin - chemistry; Lignin - metabolism; Lignocellulose; messenger RNA; Metabolism; Microbial Genetics and Genomics; Microbiology; Microorganisms; NAD (coenzyme); nalidixic acid; Purines - metabolism; reducing agents; Sensors; Studies; Tolerances; Toxic; toxicity; xanthine; xanthine dehydrogenase; Xanthines
• ISSN: 0175-7598; 1432-0614
• DOI: 10.1007/s00253-015-6450-3

In addition to glucans, xylans, and arabinans, lignocellulosic biomass hydrolysates contain significant levels of nonsugar components that are toxic to the microbes that are typically used to convert biomass to biofuels and chemicals. To enhance the tolerance of acetone–butanol–ethanol (ABE)-generating Clostridium beijerinckii NCIMB 8052 to these lignocellulose-derived microbial inhibitory compounds (LDMICs; e.g., furfural), we have been examining different metabolic perturbation strategies to increase the cellular reductant pools and thereby facilitate detoxification of LDMICs. As part of these efforts, we evaluated the effect of allopurinol, an inhibitor of NAD(P)H-generating xanthine dehydrogenase (XDH), on C. beijerinckii grown in furfural-supplemented medium and found that it unexpectedly increased the rate of detoxification of furfural by 1.4-fold and promoted growth, butanol, and ABE production by 1.2-, 2.5-, and 2-fold, respectively. Since NAD(P)H/NAD(P)⁺levels in C. beijerinckii were largely unchanged upon allopurinol treatment, we postulated and validated a possible basis in DNA repair to account for the solventogenic gains with allopurinol. Following the observation that supplementation of allopurinol in the C. beijerinckii growth media mitigates the toxic effects of nalidixic acid, a DNA-damaging antibiotic, we found that allopurinol elicited 2.4- and 6.7-fold increase in the messenger RNA (mRNA) levels of xanthine and hypoxanthine phosphoribosyltransferases, key purine-salvage enzymes. Consistent with this finding, addition of inosine (a precursor of hypoxanthine) and xanthine led to 1.4- and 1.7-fold increase in butanol production in furfural-challenged cultures of C. beijerinckii. Taken together, our results provide a purine salvage-based rationale for the unanticipated effect of allopurinol in improving furfural tolerance of the ABE-fermenting C. beijerinckii.