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Lag in adaptation to lactose as a probe to the timing of permease incorporation into the cell membrane.将乳糖作为一种探针来研究通透酶掺入细胞膜的时间时,适应过程存在滞后现象。
J Bacteriol. 1975 Oct;124(1):435-44. doi: 10.1128/jb.124.1.435-444.1975.
2
Expression and regulation of lactose genes carried by plasmids.质粒携带的乳糖基因的表达与调控。
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Studies on beta-galactoside transport in a Proteus mirabilis merodiploid carrying an Escherichia coli lactose operon.对携带大肠杆菌乳糖操纵子的奇异变形杆菌部分二倍体中β-半乳糖苷转运的研究。
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本文引用的文献

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ENZYME INDUCTION AS AN ALL-OR-NONE PHENOMENON.酶诱导作为一种全或无现象。
Proc Natl Acad Sci U S A. 1957 Jul 15;43(7):553-66. doi: 10.1073/pnas.43.7.553.
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Chemical studies in host-virus interactions; a comparison of some properties of three mutant pairs of bacterial viruses, T2r and T2r, T4r and T4r, T6r and T6r.宿主-病毒相互作用的化学研究;三对细菌病毒突变体T2r与T2r、T4r与T4r、T6r与T6r某些特性的比较
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The repression of constitutive beta-galactosidase in Escherichia coli by glucose and other carbon sources.葡萄糖及其他碳源对大肠杆菌中组成型β-半乳糖苷酶的抑制作用。
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Catabolite repression.分解代谢物阻遏
Cold Spring Harb Symp Quant Biol. 1961;26:249-56. doi: 10.1101/sqb.1961.026.01.031.
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Galactosidases.半乳糖苷酶
Adv Carbohydr Chem. 1961;16:239-98. doi: 10.1016/s0096-5332(08)60264-7.
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Growth, cell and nuclear divisions in some bacteria.某些细菌中的生长、细胞分裂和核分裂
J Gen Microbiol. 1962 Nov;29:421-34. doi: 10.1099/00221287-29-3-421.
7
Analysis of the differentiation and of the heterogeneity within a population of Escherichia coli undergoing induced beta-galactosidase synthesis.对正在进行诱导型β-半乳糖苷酶合成的大肠杆菌群体内的分化和异质性进行分析。
J Bacteriol. 1959 Nov;78(5):613-23. doi: 10.1128/jb.78.5.613-623.1959.
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Sequential transcription of the genes of the lactose operon and its regulation by protein synthesis.乳糖操纵子基因的顺序转录及其通过蛋白质合成的调控。
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9
Synthesis, utilization and degradation of lactose operon mRNA in Escherichia coli.大肠杆菌中乳糖操纵子mRNA的合成、利用与降解
J Mol Biol. 1967 Mar 14;24(2):247-59. doi: 10.1016/0022-2836(67)90330-0.
10
The adaptive responses of Escherichia coli to a feast and famine existence.大肠杆菌对丰饶与匮乏生存环境的适应性反应。
Adv Microb Physiol. 1971;6:147-217. doi: 10.1016/s0065-2911(08)60069-7.

将乳糖作为一种探针来研究通透酶掺入细胞膜的时间时,适应过程存在滞后现象。

Lag in adaptation to lactose as a probe to the timing of permease incorporation into the cell membrane.

作者信息

Koch A L

出版信息

J Bacteriol. 1975 Oct;124(1):435-44. doi: 10.1128/jb.124.1.435-444.1975.

DOI:10.1128/jb.124.1.435-444.1975
PMID:1100610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC235912/
Abstract

If bacteria are incapable of forming and incorporating proteins into the cytoplasmic membranes in all phases of the cell cycle, then not all cells from an asynchronous culture should be capable of growth when switched to a new carbon and energy source whose metabolism requires new membrane function. The transfer of an inducible culture to low lactose provides such a situation since the cells cannot grow unless galactoside permease can function to concentrate the lactose internally. From such experiments, it was concluded that the Y gene product of the lac operon is synthesized, incorporated, and can start functioning in active transport, at any time throughout the bulk of the cell cycle. Not only were the lags before growth re-ensued much shorter than would be expected if the membrane transport capability could only be developed in a small portion of the cycle, but brief pulses of a gratuitous inducer shortened the lags much further. Three types of Escherichia coli ML 30 culture were studied: cells that had exhausted the limiting glucose; cells taken directly from glucose-limited chemostats; and a washed suspension of highly catabolite repressed cells from cultures grown in high levels of glucose and gluconate. The growth studies reported here were performed on-line with a minicomputer. They represent at least an order of magnitude increase in accuracy in estimating growth parameters over previous instrumentation.

摘要

如果细菌在细胞周期的所有阶段都无法形成蛋白质并将其整合到细胞质膜中,那么当将来自异步培养物的所有细胞切换到一种新的碳源和能源时,并非所有细胞都应能够生长,因为这种新源的代谢需要新的膜功能。将可诱导培养物转移到低乳糖环境中就提供了这样一种情况,因为除非半乳糖苷通透酶能够发挥作用在细胞内部浓缩乳糖,否则细胞无法生长。从这些实验可以得出结论,乳糖操纵子的Y基因产物在细胞周期的大部分时间内随时都能合成、整合并开始在主动运输中发挥作用。生长重新开始之前的延迟时间不仅比预期的要短得多,如果膜运输能力只能在细胞周期的一小部分时间内形成的话,而且加入短暂的 gratuitous诱导剂脉冲会进一步缩短延迟时间。研究了三种类型的大肠杆菌ML 30培养物:耗尽了有限葡萄糖的细胞;直接从葡萄糖限制恒化器中取出的细胞;以及从在高浓度葡萄糖和葡萄糖酸盐中生长的培养物中洗涤得到的高度分解代谢物阻遏细胞的悬浮液。这里报道的生长研究是使用小型计算机在线进行的。与以前的仪器相比,它们在估计生长参数方面的准确性至少提高了一个数量级。