4.5 Article

L-amino acids affect the hydrogenase activity and growth of Ralstonia eutropha H16

Journal

AMB EXPRESS
Volume 13, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1186/s13568-023-01535-w

Keywords

L-Amino acids; Ralstonia eutropha H16; O-2-tolerant Hydrogenases; H-2-oxidizing Hydrogenase activity; Biocatalysts

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The addition of L-amino acids and vitamins from yeast extract enhances the synthesis and activity of O-2-tolerant Hyds enzymes in Ralstonia eutropha H16. The presence of L-amino acids leads to a decrease in pH and reduction in ORP, promoting bacterial growth and Hyds enzyme activity. These findings are crucial for optimizing the production of O-2-tolerant Hyds enzymes as anode biocatalysts.
Ralstonia eutropha H16 is a chemolithoautotrophic bacterium with O-2-tolerant hydrogenase (Hyds) enzymes. Hyds are expressed in the presence of gas mixtures (H-2, O-2, CO2) or under energy limitation and stress conditions. O-2-tolerant Hyds are promising candidates as anode biocatalysts in enzymatic fuel cells (EFCs). Supplementation of 0.5% (w/v) yeast extract to the fructose-nitrogen (FN) growth medium enhanced H-2-oxidizing Hyd activity similar to sixfold. Our study aimed to identify key metabolites (L-amino acids (L-AAs) and vitamins) in yeast extract that are necessary for the increased synthesis and activity of Hyds. A decrease in pH and a reduction in ORP (from + 240 +/- 5 mV to - 180 mV +/- 10 mV values) after 24 h of growth in the presence of AAs were observed. Compared to the FN-medium control, supplementation of 7.0 mu mol/ml of the L-AA mixture stimulated the growth of bacteria similar to 1.9 to 2.9 fold, after 72 h. The whole cells' H-2-oxidizing Hyd activity was not observed in control samples, whereas the addition of L-AAs, mainly glycine resulted in a maximum of similar to 22 +/- 0.5 and 15 +/- 0.3 U, g CDW-1 activity after 24 h and 72 h, respectively. Our results suggest a correlation between ORP, pH, and function of Hyds in R. eutropha H16 in the presence of key L-AAs. L-AAs used in small amounts can be proposed as signaling molecules or key components of Hyd maturation. These results are important for the optimization of O-2-tolerant Hyds production as anode biocatalysts.

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