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Purification and properties of glycerol kinase from Escherichia coli.

作者信息

Hayashi S I, Lin E C

出版信息

J Biol Chem. 1967 Mar 10;242(5):1030-5.

PMID:5335908
Abstract
摘要

相似文献

1
Purification and properties of glycerol kinase from Escherichia coli.大肠杆菌甘油激酶的纯化及性质
J Biol Chem. 1967 Mar 10;242(5):1030-5.
2
Glyceraldehyde phosphate dehydrogenase, phosphoglycerate kinase, and phosphoglyceromutase of Escherichia coli. Simultaneous purification and physical properties.大肠杆菌的磷酸甘油醛脱氢酶、磷酸甘油酸激酶和磷酸甘油变位酶。同步纯化及物理性质
J Biol Chem. 1971 Jul 10;246(13):4319-25.
3
Glycerol kinase.甘油激酶
Methods Enzymol. 1975;42:148-56. doi: 10.1016/0076-6879(75)42109-7.
4
Crystalline L-ribulokinase from Escherichia coli.来自大肠杆菌的结晶L-核糖激酶。
J Biol Chem. 1967 May 10;242(9):2043-50.
5
Composition and subunit structure of glycerol kinase from Escherichia coli.大肠杆菌甘油激酶的组成与亚基结构
J Biol Chem. 1971 Jun 25;246(12):3885-94.
6
Purification and characterization of adenylate kinase as an apparent adenosine triphosphate-dependent inhibitor of ribonuclease II in Escherichia coli.
J Biol Chem. 1973 Mar 25;248(6):2014-21.
7
The stereochemical course of D-glyceraldehyde-induced ATPase activity of glycerokinase from Escherichia coli.D-甘油醛诱导的大肠杆菌甘油激酶ATP酶活性的立体化学过程。
Eur J Biochem. 1988 Jun 1;174(2):387-9. doi: 10.1111/j.1432-1033.1988.tb14109.x.
8
Kinase replacement by a dehydrogenase for Escherichia coli glycerol utilization.通过脱氢酶替代激酶实现大肠杆菌对甘油的利用。
J Bacteriol. 1977 Sep;131(3):1026-8. doi: 10.1128/jb.131.3.1026-1028.1977.
9
Biogenesis of cocarboxylase in Escherichia coli. Partial purification and some properties of thiamine monophosphate kinase.大肠杆菌中羧化辅酶的生物合成。硫胺素单磷酸激酶的部分纯化及某些性质
J Biochem. 1972 Nov;72(5):1093-100. doi: 10.1093/oxfordjournals.jbchem.a129996.
10
Phosphorylation of glycerol in Staphylococcus aureus.金黄色葡萄球菌中甘油的磷酸化作用
J Bacteriol. 1973 May;114(2):880-1. doi: 10.1128/jb.114.2.880-881.1973.

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Chemical and Metabolic Controls on Dihydroxyacetone Metabolism Lead to Suboptimal Growth of Escherichia coli.化学和代谢控制对二羟丙酮代谢的影响导致大肠杆菌生长不佳。
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The sole introduction of two single-point mutations establishes glycerol utilization in CEN.PK derivatives.仅引入两个单点突变就可使CEN.PK衍生物利用甘油。
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Recombinant expression of glpK and glpD genes improves the accumulation of shikimic acid in E. coli grown on glycerol.glpK和glpD基因的重组表达提高了在甘油上生长的大肠杆菌中莽草酸的积累。
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