组氨酸
操纵子
大肠杆菌
突变体
衰减器(电子)
野生型
半乳糖操纵子
生物
L-阿拉伯糖操纵子
生物化学
基因
分子生物学
遗传学
酶
衰减
物理
光学
作者
V. G. Doroshenko,A. O. Lobanov,E. A. Fedorina
出处
期刊:Prikladnaâ biohimiâ i mikrobiologiâ
[Pleiades Publishing]
日期:2013-01-01
卷期号:49 (2): 149-154
被引量:3
标识
DOI:10.7868/s0555109913020037
摘要
Strain MG 1655+hisGr hisL'-Delta, purR, which produces histidine with a weight yield of approximately 12% from glucose, was constructed through directed chromosomal modifications of the laboratory Escherichia coli strain MG 1655+, which has a known genome sequence. A feedback-resistant ATP-phosphoribosyl transferase encoded by the mutant hisGr (E271 K) was the main determinant of histidine production. A further increase in histidine production was achieved by the expression enhance of a mutant his operon containing hisGr through the deleting attenuator region (hisL'-Delta). An increase in the expression of the wildtype his operon did not result in histidine accumulation. Deletion of the transcriptional regulator gene purR increased the biomass produced and maintained the level of histidine production per cell under the fermentation conditions used.
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