Cloning and characterization of the lactate dehydrogenase genes from Lactobacillus sp RKY2

被引:9
作者
Lee, JH
Choi, MH
Kang, HK
Ryu, HW
Sunwo, CS
Wee, YJ
Park, KD
Kim, DW
Kim, D [1 ]
机构
[1] Chonnam Natl Univ, Inst Engn Res, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Dept Mat & Biochem Engn, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Sch Biol Sci & Technol, Kwangju 500757, South Korea
[4] Chonnam Natl Univ, Res Inst Catalysis, Kwangju 500757, South Korea
[5] Chonnam Natl Univ, Korea Basic Sci Inst Gwang Ju Branch, Kwangju 500757, South Korea
[6] Kangnung Natl Univ, Dept Phys, Kangnung 210702, South Korea
[7] Dongshin Univ, Biol Res Ctr Ind Accelerator, Naju 520714, Jeonnam, South Korea
关键词
lactic acid; lactate dehydrogenase; Lactobacillus; homofermentative; gene; cloning;
D O I
10.1007/BF02942351
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 and IdhD) encoding the L-(+) and D-(-) lactate dehydrogenases (L-LDH and D-LDH) were cloned from Lactobacillus sp., RKY2, which is a lactic acid hyper-producing bacterium isolated from Kimchi. Open reading frames of IdhL for and IdhD 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 of Lactobacillus plantarum. The conserved residues in the catalytic activity and substrate binding of both LDHs were identified in both enzymes.
引用
收藏
页码:318 / 322
页数:5
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