Affiliation:
1. State Key Laboratory of Microbial Technology, Shandong University, Jinan, People's Republic of China
2. State Key Laboratory of Microbial Metabolism and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, People's Republic of China
Abstract
ABSTRACT
d
-Lactate was identified as one of the few available organic acids that supported the growth of
Gluconobacter oxydans
621H in this study. Interestingly, the strain used
d
-lactate as an energy source but not as a carbon source, unlike other lactate-utilizing bacteria. The enzymatic basis for the growth of
G. oxydans
621H on
d
-lactate was therefore investigated. Although two putative NAD-independent
d
-lactate dehydrogenases, GOX1253 and GOX2071, were capable of oxidizing
d
-lactate, GOX1253 was the only enzyme able to support the
d
-lactate-driven growth of the strain. GOX1253 was characterized as a membrane-bound dehydrogenase with high activity toward
d
-lactate, while GOX2071 was characterized as a soluble oxidase with broad substrate specificity toward
d
-2-hydroxy acids. The latter used molecular oxygen as a direct electron acceptor, a feature that has not been reported previously in
d
-lactate-oxidizing enzymes. This study not only clarifies the mechanism for the growth of
G. oxydans
on
d
-lactate, but also provides new insights for applications of the important industrial microbe and the novel
d
-lactate oxidase.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
20 articles.
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