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Cloning and characterization of the lactate dehydrogenase genes fromLactobacillus sp. RKY2
Authors:Jin-Ha?Lee,Mi-Hwa?Choi,Ji-Young?Park,Hee-Kyoung?Kang,Hwa-Won?Ryu,Chang-Sin?Sunwo,Young-Jung?Wee,Ki-Deok?Park,Do-Won?Kim,Doman?Kim  author-information"  >  author-information__contact u-icon-before"  >  mailto:dmkim@chonnam.ac.kr"   title="  dmkim@chonnam.ac.kr"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People’s Republic of China;(2) Key Laboratory of Systems Bioengineering (Tianjin University), Ministry of Education, Tianjin, 300072, People’s Republic of China;
Abstract:Lactic acid is an environmentally benign organic acid that could be used as a raw material for biodegradable plastics if it can be inexpensively produced by fermentation. Two genes (IdhL andIdhD) encoding the L-(+) and D-(−) lactate dehydrogenases (L-LDH and D-LDH) were cloned fromLactobacillus sp., RKY2, which is a lactic acid hyper-producing bacterium isolated from Kimchi. Open reading frames ofIdhL for andIdhD for the L and D-LDH genes were 962 and 998 bp, respectively. Both the L(+)- and D(−)-LDH proteins showed the highest degree of homology with the L- and D-lactate dehydrogenase genes ofLactobacillus plantarum. The conserved residues in the catalytic activity and substrate binding of both LDHs were identified in both enzymes.
Keywords:lactic acid  lactate dehydrogenase   Lactobacillus   homofermentative  gene  cloning
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