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Coregulation of beta-galactoside uptake and hydrolysis by the hyperthermophilic bacterium Thermotoga neapolitana

机译:β-半乳糖苷的摄取和高温嗜热菌Theromotoga neapolitana的水解共调节

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Regulation of the beta-galactoside transport system in response to growth substrates in the extremely thermophilic anaerobic bacterium Thermotoga neapolitana was studied with the nonmetabolizable analog methyl-beta-D-thiogalactopyranoside (TMG) as the transport substrate. T. neapolitana cells grown on galactose or lactose accumulated TMG against a concentration gradient in an intracellular free sugar pool that was exchangeable with external galactose or lactose and showed induced levels of beta-galactosidase. Cells grown on glucose, maltose, or galactose plus glucose showed no capacity to accumulate TMG, though these cells carried out active transport of the nonmetabolizable glucose analog 2-deoxy-D-glucose. Glucose neither inhibited TMG uptake nor caused efflux of preaccumulated TMG; rather, glucose promoted TMG uptake by supplying metabolic energy. These data show that beta-D-galactosides are taken up by T. neapolitana via an active transport system that can be induced by galactose or lactose and repressed by glucose but which is not inhibited by glucose. Thus, the phenomenon of catabolite repression is present in T. neapolitana with respect to systems catalyzing both the transport and hydrolysis of beta-D-galactosides, but inducer exclusion and inducer expulsion, mechanisms that regulate permease activity, are not present. Regulation is manifest at the level of synthesis of the beta-galactoside transport system but not in the activity of the system.
机译:研究了β-半乳糖苷转运系统对极端嗜热厌氧细菌嗜热栖热菌的生长底物的响应,以不可代谢的类似物甲基-β-D-硫代半乳糖吡喃糖苷(TMG)作为转运底物。在半乳糖或乳糖上生长的T. neapolitana细胞在细胞内游离糖池中的浓度梯度下积累了TMG,该池可与外部半乳糖或乳糖交换并显示出诱导水平的β-半乳糖苷酶。在葡萄糖,麦芽糖或半乳糖加葡萄糖上生长的细胞没有积聚TMG的能力,尽管这些细胞对不可代谢的葡萄糖类似物2-deoxy-D-葡萄糖进行了主动转运。葡萄糖既不能抑制TMG的摄取,也不会引起预积累的TMG的流出。相反,葡萄糖通过提供代谢能量来促进TMG摄取。这些数据表明,β-D-半乳糖苷被T. neapolitana通过主动转运系统吸收,该系统可以被半乳糖或乳糖诱导并被葡萄糖抑制,但不受葡萄糖抑制。因此,就催化β-D-半乳糖苷的运输和水解的系统而言,在那不勒斯烟草中存在分解代谢物阻抑的现象,但是不存在调节渗透酶活性的机制的诱导物排斥和诱导物排出。调节作用是在β-半乳糖苷转运系统的合成水平上体现出来的,而不是在该系统的活性方面表现出来。

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