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中国精品科技期刊2020
谭才邓, 朱美娟, 廖延智, 朱晓立. 乙酸异戊酯高产菌株脂肪酶基因Lip2的克隆及表达研究[J]. 食品工业科技, 2016, (01): 153-155. DOI: 10.13386/j.issn1002-0306.2016.01.023
引用本文: 谭才邓, 朱美娟, 廖延智, 朱晓立. 乙酸异戊酯高产菌株脂肪酶基因Lip2的克隆及表达研究[J]. 食品工业科技, 2016, (01): 153-155. DOI: 10.13386/j.issn1002-0306.2016.01.023
TAN Cai- deng, ZHU Mei- juan, LIAO Yan- zhi, ZHU Xiao- li. Study on the cloning and prokaryotic soluble expression of Lipase gene Lip2 of high- yield isoamyl acetate strain[J]. Science and Technology of Food Industry, 2016, (01): 153-155. DOI: 10.13386/j.issn1002-0306.2016.01.023
Citation: TAN Cai- deng, ZHU Mei- juan, LIAO Yan- zhi, ZHU Xiao- li. Study on the cloning and prokaryotic soluble expression of Lipase gene Lip2 of high- yield isoamyl acetate strain[J]. Science and Technology of Food Industry, 2016, (01): 153-155. DOI: 10.13386/j.issn1002-0306.2016.01.023

乙酸异戊酯高产菌株脂肪酶基因Lip2的克隆及表达研究

Study on the cloning and prokaryotic soluble expression of Lipase gene Lip2 of high- yield isoamyl acetate strain

  • 摘要: 通过PCR扩增了乙酸异戊酯高产菌Loq-c的脂肪酶基因Lip2,其序列与Gene Bank中的Candida cylindracea Lip2 gene(序列号X64704.1)的序列相似度最高,为89%。构建原核表达载体p QE-lip2,转化大肠杆菌E.coli BL21(DE3),获得了重组菌BL21(p QE-lip2)。经过表达条件探索,用SDS聚丙烯酰胺凝胶电泳分析,脂肪酶Lip2原核可溶表达最佳条件为:诱导温度30℃,IPTG使用浓度为1.5 mmol/L,150 r/min转速的条件下诱导表达5 h。 

     

    Abstract: The gene encoding Lipase2( Lip2) from high- yield isoamyl acetate strain Loq- c was amplified by polymerase chain reaction( PCR),its sequence was most similar to Candida cylindracea Lip2 gene( X64704.1),the similarity was 89%.Subsequently,the corresponding expression vector p QE- lip2 was constructed and cloned into E.coli BL21( DE3),resulting in recombinant strain BL21( p QE- lip2).After explorations,SDS- PAGE analysis showed that the best conditions for soluble expression of Lip2 was: 30 ℃,IPTG 1.5 mmol / L,150 r / min,induced for 5 hours.

     

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