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Osmotic Adaptation of Thermus thermophilus RQ-1: Lesson from a Mutant Deficient in Synthesis of Trehalose

机译:嗜热栖热菌RQ-1的渗透适应:缺乏海藻糖合成的突变的教训

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摘要

Strains of Thermus thermophilus accumulate primarily trehalose and smaller amounts of mannosylglycerate in response to salt stress in yeast extract-containing media (O. C. Nunes, C. M. Manaia, M. S. da Costa, and H. Santos, Appl. Environ. Microbiol. 61:2351-2357, 1995). A 2.4-kbp DNA fragment from T. thermophilus strain RQ-1 carrying otsA (encoding trehalose-phosphate synthase [TPS]), otsB (encoding trehalose-phosphate phosphatase [TPP]), and a short sequence of the 5′ end of treS (trehalose synthase [TreS]) was cloned from a gene library. The sequences of the three genes (including treS) were amplified by PCR and sequenced, revealing that the genes were structurally linked. To understand the role of trehalose during salt stress in T. thermophilus RQ-1, we constructed a mutant, designated RQ-1M6, in which TPS (otsA) and TPP (otsB) genes were disrupted by gene replacement. Mutant RQ-1M6 accumulated trehalose and mannosylglycerate in a medium containing yeast extract and NaCl. However, growth in a defined medium (without yeast extract, known to contain trehalose) containing NaCl led to the accumulation of mannosylglycerate but not trehalose. The deletion of otsA and otsB reduced the ability to grow in defined salt-containing medium, with the maximum salinity being 5% NaCl for RQ-1 and 3% NaCl for RQ-1M6. The lower salt tolerance observed in the mutant was relieved by the addition of trehalose to the growth media. In contrast to trehalose, the addition of glycine betaine, mannosylglycerate, maltose, and glucose to the growth medium did not allow the mutant to grow at higher salinities. The results presented here provide crucial evidence for the importance of the TPS/TPP pathway for the synthesis and accumulation of trehalose and the decisive contribution of this disaccharide to osmotic adaptation in T. thermophilus RQ-1.
机译:嗜盐栖热菌菌株在含酵母提取物的培养基中响应盐胁迫而主要积累海藻糖和少量甘露糖基甘油酸酯(OC Nunes,CM Manaia,MS da Costa和H.Santos,Appl.Environ.Microbiol.61:2351-2357)。 (1995年)。嗜热链球菌菌株RQ-1的一个2.4 kbp DNA片段,带有otsA(编码海藻糖磷酸合酶[TPS]),otsB(编码海藻糖磷酸磷酸酶[TPP])和treS 5'末端的短序列(海藻糖合酶[TreS])从基因文库中克隆。通过PCR扩增并测序了三个基因(包括treS)的序列,揭示了这些基因在结构上相连。为了了解海藻糖在嗜盐热单胞菌RQ-1的盐胁迫中的作用,我们构建了一个命名为RQ-1M6的突变体,其中的TPS(otsA)和TPP(otsB)基因被基因置换破坏。突变体RQ-1M6在含有酵母提取物和NaCl的培养基中积累了海藻糖和甘露糖基甘油酸酯。但是,在含有NaCl的特定培养基(无酵母提取物,已知含有海藻糖)中的生长会导致甘露糖基甘油酸而不是海藻糖的积累。 otsA和otsB的缺失降低了在限定的含盐培养基中生长的能力,RQ-1的最大盐度为5%NaCl,RQ-1M6的最大盐度为3%NaCl。向生长培养基中添加海藻糖可以缓解突变体中较低的耐盐性。与海藻糖相反,向生长培养基中添加甘氨酸甜菜碱,甘露糖基甘油酸酯,麦芽糖和葡萄糖不能使突变体在更高盐度下生长。此处提供的结果为TPS / TPP途径对海藻糖的合成和积累的重要性以及该二糖对嗜热链球菌RQ-1渗透适应的决定性贡献提供了重要证据。

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