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XIE Yu-qing;LUO Shu-ping;Mao Jun
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谢玉清;罗淑萍;茆军
摘要: 利用PCR技术以L-丝氨酸产生菌株黄色短杆菌c-11的染色体DNA为摸板,扩增出serA基因,连接到表达载体pEC7上,转化L-丝氨酸产生菌c-11,使其氨基酸产量由12 g/L增加到18 g/L,产酸率增加了50;.
XIE Yu-qing;LUO Shu-ping;Mao Jun. Cloning and Expression of SerA in C-11 Producing L-serine[J]. .
谢玉清;罗淑萍;茆军. L-丝氨酸产生菌c-11中serA基因的克隆与表达[J]. .
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