Cargando…
l-amino acids affect the hydrogenase activity and growth of Ralstonia eutropha H16
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), CO(2)) or under energy limitation and stress conditions. O(2)-tolerant Hyds are promising candidates as anode biocatalysts in enz...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023824/ https://www.ncbi.nlm.nih.gov/pubmed/36932299 http://dx.doi.org/10.1186/s13568-023-01535-w |
Sumario: | 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), CO(2)) 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 ~ 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 μmol/ml of the l-AA mixture stimulated the growth of bacteria ~ 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 ~ 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. |
---|