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A two-stage temperature control strategy enhances extracellular secretion of recombinant α-cyclodextrin glucosyltransferase in Escherichia coli

机译：两级温度控制策略增强了大肠杆菌中重组α-环糊精的细胞外分泌葡萄糖基转移酶

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Yang Li; Jia Liu; Yinglan Wang; Bingjie Liu; Xiaofang Xie; Rui Jia; Caiming Li; Zhaofeng Li;
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1. Delayed supplementation of glycine enhances extracellular secretion of the recombinant α-cyclodextrin glycosyltransferase in Escherichia coli [J] . Li Z., Gu Z., Wang M., Applied Microbiology and Biotechnology . 2010,第3期

机译：延迟补充甘氨酸可增强大肠杆菌中重组α-环糊精糖基转移酶的细胞外分泌
2. Delayed supplementation of glycine enhances extracellular secretion of the recombinant α-cyclodextrin glycosyltransferase in Escherichia coli [J] . Zhaofeng Li, Zhengbiao Gu, Miao Wang, Applied Microbiology and Biotechnology . 2010,第3期

机译：延迟补充甘氨酸可增强大肠杆菌中重组α-环糊精糖基转移酶的细胞外分泌
3. Calcium Leads to Further Increase in Glycine-Enhanced Extracellular Secretion of Recombinant o-Cyclodextrin GlycosyItransferase in Escherichia coli [J] . Journal of Agricultural and Food Chemistry . 2009,第14期

机译：钙导致大肠杆菌中o-环糊精糖基转移酶的甘氨酸增强细胞外分泌进一步增加
4. Optimization of production medium for expression and secretion of a heterologous cutinase by a recombinant Escherichia coli strain [C] . João Prazeres, Luís Fonseca, Fátima N. Serralha IEEE Portuguese Meeting in Bioengineering . 2019

机译：重组大肠杆菌菌株表达和分泌异源角质酶的生产培养基的优化
5. Engineering the central carbon metabolism of Escherichia coli to enhance organic acid secretion [D] . Elias, Jisha. 2009

机译：工程化大肠杆菌的中央碳代谢，以增强有机酸的分泌
6. A two-stage temperature control strategy enhances extracellular secretion of recombinant α-cyclodextrin glucosyltransferase in Escherichia coli [O] . Yang Li, Jia Liu, Yinglan Wang, 2017

机译：两阶段温度控制策略增强了大肠杆菌中重组α-环糊精葡萄糖基转移酶的细胞外分泌
7. Optimization extracellular secretion of Recombinant Human Epidermal Growth Factor (hEGF) in Escherichia coli BL21 (DE3) pD881-OmpA-hEGF by using Response Surface Method (RSM) [O] . 2019

机译：用响应表面法（RSM）优化大肠杆菌BL21（DE3）PD881-OMPA-HEGF重组人表皮生长因子（HEGF）的细胞外分泌

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A two-stage temperature control strategy enhances extracellular secretion of recombinant α-cyclodextrin glucosyltransferase in Escherichia coli

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