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乙醇对大肠杆菌的可逆作用。

Reversible effects of ethanol on E. coli.

作者信息

Ingram L O, Dickens B F, Buttke T M

出版信息

Adv Exp Med Biol. 1980;126:299-337. doi: 10.1007/978-1-4684-3632-7_24.

DOI:10.1007/978-1-4684-3632-7_24
PMID:6447436
Abstract

Chronic exposure of E. coli to ethanol during growth resulted in major changes in lipid composition. These ethanol-induced changes, a decrease in the proportion of saturated fatty acids, are similar to those which occur following a shift to lower temperature. Products of ethanol metabolism such as acetaldehyde and acetate caused the opposite changes in fatty acid composition. In vivo studies using mutants blocked in lipid synthesis indicated that saturated fatty acid synthesis was the primary target leading to changes in bulk lipid fatty acid composition. This was confirmed in vitro and condensing enzyme II was identified as the probable site of ethanol inhibition. The acute affects of ethanol on the function of two membrane-bound enzymes, Mg++ATPase and lac permease were also examined. In both cases, cells grown in the presence of ethanol. In time-course studies, permease function was restored concurrently with changes in lipid composition. Mutants were isolated which were able to grow in the presence of high levels of ethanol. These mutants displayed exaggerated changes in lipid composition providing evidence that alcohol-resistance and fatty acid changes are related.

摘要

在生长过程中,大肠杆菌长期暴露于乙醇会导致脂质组成发生重大变化。这些由乙醇诱导的变化,即饱和脂肪酸比例的降低,与温度降低后发生的变化相似。乙醇代谢产物如乙醛和乙酸会导致脂肪酸组成发生相反的变化。使用脂质合成受阻的突变体进行的体内研究表明,饱和脂肪酸合成是导致总体脂质脂肪酸组成变化的主要靶点。这在体外得到了证实,并且缩合酶II被确定为乙醇抑制的可能位点。还研究了乙醇对两种膜结合酶Mg++ATPase和乳糖通透酶功能的急性影响。在这两种情况下,细胞都是在乙醇存在下生长的。在时间进程研究中,通透酶功能随着脂质组成的变化而同时恢复。分离出了能够在高浓度乙醇存在下生长的突变体。这些突变体在脂质组成上表现出夸张的变化,这证明了抗酒精性和脂肪酸变化是相关的。

相似文献

1
Reversible effects of ethanol on E. coli.乙醇对大肠杆菌的可逆作用。
Adv Exp Med Biol. 1980;126:299-337. doi: 10.1007/978-1-4684-3632-7_24.
2
Mechanism of ethanol-induced changes in lipid composition of Escherichia coli: inhibition of saturated fatty acid synthesis in vivo.乙醇诱导大肠杆菌脂质组成变化的机制:体内饱和脂肪酸合成的抑制
Biochemistry. 1978 Feb 21;17(4):637-44. doi: 10.1021/bi00597a012.
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Alcohol tolerance in Escherichia coli.大肠杆菌中的酒精耐受性。
Pharmacol Biochem Behav. 1980;13 Suppl 1:191-5. doi: 10.1016/s0091-3057(80)80030-x.
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Localization of the galactoside binding site in the lactose carrier of Escherichia coli.
Biochim Biophys Acta. 1984 Oct 3;776(2):247-58. doi: 10.1016/0005-2736(84)90214-1.
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Active transport in Escherichia coli: passage to permease.大肠杆菌中的主动运输:通向通透酶的过程。
Annu Rev Biophys Biophys Chem. 1986;15:279-319. doi: 10.1146/annurev.bb.15.060186.001431.
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Proton electrochemical gradients and active transport: the saga of lac permease.质子电化学梯度与主动运输:乳糖通透酶的故事
Ann N Y Acad Sci. 1985;456:291-304. doi: 10.1111/j.1749-6632.1985.tb14879.x.
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Ethanol-induced changes in lipid composition of Escherichia coli: inhibition of saturated fatty acid synthesis in vitro.乙醇诱导的大肠杆菌脂质组成变化:体外对饱和脂肪酸合成的抑制
Arch Biochem Biophys. 1980 Sep;203(2):565-71. doi: 10.1016/0003-9861(80)90213-1.
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Regulation of fatty acid composition in Escherichia coli: a proposed common mechanism for changes induced by ethanol, chaotropic agents, and a reduction of growth temperature.大肠杆菌中脂肪酸组成的调控:乙醇、离液剂及生长温度降低所诱导变化的一种可能共同机制
J Bacteriol. 1982 Jan;149(1):166-72. doi: 10.1128/jb.149.1.166-172.1982.
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A nontransportable substrate for lactose permease.乳糖通透酶的一种不可转运的底物。
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Site-directed mutagenesis of cysteine-148 in the lac permease of Escherichia coli: effect on transport, binding, and sulfhydryl inactivation.大肠杆菌乳糖通透酶中半胱氨酸-148的定点诱变:对转运、结合及巯基失活的影响
Biochemistry. 1985 Dec 17;24(26):7628-35. doi: 10.1021/bi00347a020.

引用本文的文献

1
Systems-level understanding of ethanol-induced stresses and adaptation in E. coli.大肠杆菌中乙醇诱导的应激和适应的系统水平理解。
Sci Rep. 2017 Mar 16;7:44150. doi: 10.1038/srep44150.
2
Differential effects of ethanol and hexanol on the Escherichia coli cell envelope.乙醇和己醇对大肠杆菌细胞膜的不同作用
J Bacteriol. 1980 Nov;144(2):481-8. doi: 10.1128/jb.144.2.481-488.1980.
3
Lipid composition of Zymomonas mobilis: effects of ethanol and glucose.运动发酵单胞菌的脂质组成:乙醇和葡萄糖的影响
J Bacteriol. 1983 Jun;154(3):1291-300. doi: 10.1128/jb.154.3.1291-1300.1983.