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Mutants of Escherichia coli K 12 altered in their ability to store glycogen.

作者信息

Damotte M, Cattanéo J, Sigal N, Puig J

出版信息

Biochem Biophys Res Commun. 1968 Sep 30;32(6):916-20. doi: 10.1016/0006-291x(68)90114-9.

DOI:10.1016/0006-291x(68)90114-9
PMID:4880732
Abstract
摘要

相似文献

1
Mutants of Escherichia coli K 12 altered in their ability to store glycogen.
Biochem Biophys Res Commun. 1968 Sep 30;32(6):916-20. doi: 10.1016/0006-291x(68)90114-9.
2
Isolation of mutants of Escherichia coli B altered in their ability to synthesize glycogen.大肠杆菌B中糖原合成能力发生改变的突变体的分离。
J Bacteriol. 1969 Feb;97(2):970-2. doi: 10.1128/jb.97.2.970-972.1969.
3
Induction of closely linked multiple mutations by nitrosoguanidine.亚硝基胍诱导紧密连锁的多重突变
Nat New Biol. 1971 Mar 24;230(12):122-5. doi: 10.1038/newbio230122a0.
4
The elimination of Flac+ from Escherichia coli by mutagenic agents.诱变剂对大肠杆菌中Flac+的消除作用。
Biochem Biophys Res Commun. 1967 Apr 7;27(1):112-7. doi: 10.1016/s0006-291x(67)80048-2.
5
[On the optimum pH of mutation induction by 1-nitroso-3-nitro-1-methylguanide].[关于1-亚硝基-3-硝基-1-甲基胍诱导突变的最佳pH值]
Naturwissenschaften. 1968 Feb;55(2):85. doi: 10.1007/BF00599497.
6
[Obtaining auxotropic mutants from cultures of Escherichia coli pathogenic serotype O111:B4:H2, treated with N-methyl-N'-nitro-N-nitrosoguanidine].[从经N-甲基-N'-硝基-N-亚硝基胍处理的致病性血清型O111:B4:H2大肠杆菌培养物中获得营养缺陷型突变体]
Biull Eksp Biol Med. 1970 Feb;69(2):110-2.
7
L-Serine-sensitive mutants of Escherichia coli K-12.大肠杆菌K-12的L-丝氨酸敏感突变体。
J Bacteriol. 1970 Sep;103(3):840-1. doi: 10.1128/jb.103.3.840-841.1970.
8
[Screening test on anti-cancer and anti-microbial actions. 8. Mutagenic and prophage-inducing activities of 1-substituted-3-nitro-1-nitrosoguanidine derivatives. 1].
Eisei Shikenjo Hokoku. 1970;88:118-23.
9
The replication of the Escherichia coli chromosome studied by sequential nitrosoguanidine mutagenesis.通过连续亚硝基胍诱变研究大肠杆菌染色体的复制。
Cold Spring Harb Symp Quant Biol. 1968;33:599-607. doi: 10.1101/sqb.1968.033.01.066.
10
[On the mechanism of action of 1-nitroso-3-nitro-1-methylguanidine (NNMG) in mutagenesis. IV. Stability of NNMG, relations between mutation rate and uptake of the mutagen by the cell, and requirement for methylation by sulfhydryl groups as a function of the pH value].[关于1-亚硝基-3-硝基-1-甲基胍（NNMG）诱变作用的机制。IV. NNMG的稳定性、突变率与细胞对诱变剂摄取之间的关系以及巯基甲基化作为pH值函数的需求]
Z Naturforsch B. 1969 Jul;24(7):903-10.

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The heteromultimeric debranching enzyme involved in starch synthesis in Arabidopsis requires both isoamylase1 and isoamylase2 subunits for complex stability and activity.拟南芥淀粉合成中涉及的异源多聚脱支酶需要异淀粉酶 1 和异淀粉酶 2 亚基来维持复合物的稳定性和活性。
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Glycogen contributes to the environmental persistence and transmission of Vibrio cholerae.
糖原有助于霍乱弧菌在环境中的持久性和传播。
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4
Glycogen phosphorylase, the product of the glgP Gene, catalyzes glycogen breakdown by removing glucose units from the nonreducing ends in Escherichia coli.糖原磷酸化酶是glgP基因的产物，通过从大肠杆菌非还原端去除葡萄糖单位来催化糖原分解。
J Bacteriol. 2006 Jul;188(14):5266-72. doi: 10.1128/JB.01566-05.
5
Role of the Escherichia coli glgX gene in glycogen metabolism.大肠杆菌glgX基因在糖原代谢中的作用。
J Bacteriol. 2005 Feb;187(4):1465-73. doi: 10.1128/JB.187.4.1465-1473.2005.
6
Global regulatory mutations in csrA and rpoS cause severe central carbon stress in Escherichia coli in the presence of acetate.在存在乙酸盐的情况下，csrA和rpoS中的全局调控突变会导致大肠杆菌出现严重的中心碳代谢应激。
J Bacteriol. 2000 Mar;182(6):1632-40. doi: 10.1128/JB.182.6.1632-1640.2000.
7
A system to generate chromosomal mutations in Lactococcus lactis which allows fast analysis of targeted genes.一种在乳酸乳球菌中产生染色体突变的系统，可实现对目标基因的快速分析。
J Bacteriol. 1995 Dec;177(24):7011-8. doi: 10.1128/jb.177.24.7011-7018.1995.
8
Biosynthesis of bacterial glycogen: purification and properties of Salmonella typhimurium LT-2 adenosine diphosphate glucose pyrophosphorylase.细菌糖原的生物合成：鼠伤寒沙门氏菌LT-2二磷酸腺苷葡萄糖焦磷酸化酶的纯化及特性
J Bacteriol. 1980 Jul;143(1):120-7. doi: 10.1128/jb.143.1.120-127.1980.
9
Polysaccharide that may serve as a carbon and energy storage compound for sporulation in Bacillus cereus.可能作为蜡样芽孢杆菌孢子形成过程中的碳和能量储存化合物的多糖。
J Bacteriol. 1974 Oct;120(1):399-406. doi: 10.1128/jb.120.1.399-406.1974.
10
The isolation of mutants not accumulating poly-beta-hydroxybutyric acid.不积累聚β-羟基丁酸的突变体的分离
Arch Mikrobiol. 1970;71(3):283-94. doi: 10.1007/BF00410161.