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中国精品科技期刊2020
石鹏, 王永红. 凝结芽孢杆菌中与乳酸生产相关的乳酸脱氢酶基因的研究[J]. 食品工业科技, 2018, 39(24): 109-113. DOI: 10.13386/j.issn1002-0306.2018.24.020
引用本文: 石鹏, 王永红. 凝结芽孢杆菌中与乳酸生产相关的乳酸脱氢酶基因的研究[J]. 食品工业科技, 2018, 39(24): 109-113. DOI: 10.13386/j.issn1002-0306.2018.24.020
SHI Peng, WANG Yong-hong. Lactic Dehydrogenase Gene Related to Lactic Acid Production in Bacillus coagulans[J]. Science and Technology of Food Industry, 2018, 39(24): 109-113. DOI: 10.13386/j.issn1002-0306.2018.24.020
Citation: SHI Peng, WANG Yong-hong. Lactic Dehydrogenase Gene Related to Lactic Acid Production in Bacillus coagulans[J]. Science and Technology of Food Industry, 2018, 39(24): 109-113. DOI: 10.13386/j.issn1002-0306.2018.24.020

凝结芽孢杆菌中与乳酸生产相关的乳酸脱氢酶基因的研究

Lactic Dehydrogenase Gene Related to Lactic Acid Production in Bacillus coagulans

  • 摘要: 对5株凝结芽孢杆菌乳酸生产情况进行研究,并以凝结芽孢杆菌ATCC7050作为乳酸脱氢酶基因研究的对象,确定得出其乳酸生产关键的乳酸脱氢酶基因。结果表明:凝结芽孢杆菌生产的乳酸分两种类型:L型乳酸和D型乳酸,但主要以L型乳酸为主,其光学纯度达到97%以上。在凝结芽孢杆菌ATCC7050基因组中存在的ldhL1、ldhL2和ldhD三种乳酸脱氢酶基因中,ldhL2基因没有检测到转录信号,而ldhD转录水平很低,在生长对数期ldhL1基因的转录水平是ldhD基因转录水平的68倍,这说明ldhL1基因是凝结芽孢杆菌ATCC7050乳酸生产的关键性基因。本研究确定了凝结芽孢杆菌ATCC7050乳酸合成中最主要的乳酸脱氢酶基因,对凝结芽孢杆菌代谢研究和基因改造奠定了基础。

     

    Abstract: Five Bacillus coagulans strains were studied for lactic acid production,and based on the genome of B. coagulans ATCC7050,the key lactic dehydrogenase gene in lactic acid production was determined. The results showed that,there are two types of lactic acid produced by Bacillus coagulans:L-type lactic acid and D-type lactic acid,but mainly L-type lactic acid,and its optical purity was more than 97%. In the genome of Bacillus coagulans ATCC7050,there were three lactate dehydrogenase genes:ldhL1,ldhL2 and ldhD. The transcriptional signal was not detected in the ldhL2 gene,while the transcriptional level of the ldhL1 gene in the logarithmic phase was 68 times as that of the ldhD gene,which indicated that the ldhL1 gene was the key gene for lactic acid production by ATCC7050. So the most important lactic dehydrogenase gene was identified in the lactic acid synthesis in ATCC7050,and it laid the foundation for metabolic research and genetic engineering of B. coagulans.

     

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