2016
DOI: 10.1038/srep37916
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Contributory roles of two l-lactate dehydrogenases for l-lactic acid production in thermotolerant Bacillus coagulans

Abstract: Thermotolerant Bacillus coagulans is considered to be a more promising producer for bio-chemicals, due to its capacity to withstand harsh conditions. Two L-lactate dehydrogenase (LDH) encoding genes (ldhL1 and ldhL2) and one D-LDH encoding gene (ldhD) were annotated from the B. coagulans DSM1 genome. Transcriptional analysis revealed that the expression of ldhL2 was undetectable while the ldhL1 transcription level was much higher than that of ldhD at all growth phases. Deletion of the ldhL2 gene revealed no di… Show more

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Cited by 19 publications
(27 citation statements)
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“…The distinct catalytic activities of L‐ and D‐LDHs contributed to differences in the ratio of the two isomers and different types of Lactobacillus strains. In contrast to the situation in Lactobacillus strains, the ldh L transcription level in B. coagulans 2‐6 was much higher than that of ldh D in all growth phases, which might explain high optical purity of the l ‐lactate produced by this strain (Sun et al., ; Wang et al., ). Therefore, the crucial factors affecting the optical purity of lactate may differ among various LAB.…”
Section: Resultsmentioning
confidence: 85%
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“…The distinct catalytic activities of L‐ and D‐LDHs contributed to differences in the ratio of the two isomers and different types of Lactobacillus strains. In contrast to the situation in Lactobacillus strains, the ldh L transcription level in B. coagulans 2‐6 was much higher than that of ldh D in all growth phases, which might explain high optical purity of the l ‐lactate produced by this strain (Sun et al., ; Wang et al., ). Therefore, the crucial factors affecting the optical purity of lactate may differ among various LAB.…”
Section: Resultsmentioning
confidence: 85%
“…E. coli strains were grown in Luria‐Bertani (LB) medium on a rotary shaker at 37°C. Plasmid pMD18‐T was used for cloning the genes encoding LDHs, whereas plasmid pET‐28a was used to express the recombinant LDHs with a N‐terminal His‐tag (Sun et al., ; Zhou, Zhang, Meng, Zhang, & Li, ). All the reagents were of analytical grade and commercially available.…”
Section: Methodsmentioning
confidence: 99%
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