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首页> 外文期刊>Microbiology >Genetic dissection of trehalose biosynthesis in Corynebacterium glutamicum: inactivation of trehalose production leads to impaired growth and an altered cell wall lipid composition
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Genetic dissection of trehalose biosynthesis in Corynebacterium glutamicum: inactivation of trehalose production leads to impaired growth and an altered cell wall lipid composition

机译:CoryneBacterium谷氨酸中海藻糖生物合成的遗传解剖:海藻糖生产的失活导致生长受损,细胞壁脂质组合物损害

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The analysis of the available Corynebacterium genome sequence data led to the proposal of the presence of all three known pathways for trehalose biosynthesis in bacteria, i.e. trehalose synthesis from UDP-glucose and glucose 6-phosphate (OtsA-OtsB pathway), from malto-oligosaccharides or α-1,4-glucans (TreY-TreZ pathway), or from maltose (TreS pathway). Inactivation of only one of the three pathways by chromosomal deletion did not have a severe impact on C. glutamicum growth, while the simultaneous inactivation of the OtsA-OtsB and TreY-TreZ pathway or of all three pathways resulted in the inability of the corresponding mutants to synthesize trehalose and to grow efficiently on various sugar substrates in minimal media. This growth defect was largely reversed by the addition of trehalose to the culture broth. In addition, a possible pathway for glycogen synthesis from ADP-glucose involving glycogen synthase (GlgA) was discovered. C. glutamicum was found to accumulate significant amounts of glycogen when grown under conditions of sugar excess. Insertional inactivation of the chromosomal glgA gene led to the failure of C. glutamicum cells to accumulate glycogen and to the abolition of trehalose production in a ΔotsAB background, demonstrating that trehalose production via the TreY-TreZ pathway is dependent on a functional glycogen biosynthetic route. The trehalose-non-producing mutant with inactivated OtsA-OtsB and TreY-TreZ pathways displayed an altered cell wall lipid composition when grown in minimal broth in the absence of trehalose. Under these conditions, the mutant lacked both major trehalose-containing glycolipids, i.e. trehalose monocorynomycolate and trehalose dicorynomycolate, in its cell wall lipid fraction. The results suggest that a dramatically altered cell wall lipid bilayer of trehalose-less C. glutamicum mutants may be responsible for the observed growth deficiency of such strains in minimal medium. The results of the genetic and physiological dissection of trehalose biosynthesis in C. glutamicum reported here may be of general relevance for the whole phylogenetic group of mycolic-acid-containing coryneform bacteria.
机译:可用的棒状杆菌基因组序列数据的分析导致了对细菌中海藻糖生物合成的所有三种已知途径的提议,即来自MALTO-低聚糖的UDP-葡萄糖和葡萄糖6-磷酸(Otsa-ootsb途径)的海藻糖合成或α-1,4-葡聚糖(Trey-Trez途径)或来自麦芽糖(Tres途径)。染色体缺失只有三种途径中只有一个对C.谷氨酰胺生长的灭活没有严重影响,而Otsa-oTsb和Trey-trez途径或所有三种途径的同时灭活导致相应的突变体的无能为力合成海藻糖并有效地在最小培养基中有效地生长。这种生长缺陷在很大程度上通过加入培养肉汤来逆转。此外,发现了涉及糖原合酶(GLGA)的ADP-葡萄糖的糖原合成的可能途径。 C.在糖过量的条件下生长时,发现谷氨酰氨菊酯在生长时积累了大量的糖原。染色体GLGA基因的插入灭活导致C.谷氨酸细胞的失效,以积累糖原和施加在ΔAbsab背景中的海藻糖产生,证明通过Trey-Trez途径的海藻糖产生依赖于功能性糖苷生物合成途径。当不存在海藻糖时在最小肉汤中生长时,具有灭活的OTSA-OTSB和Trey-Trez途径的海藻糖 - 非产生突变体显示出改变的细胞壁脂质组合物。在这些条件下,突变体缺乏含有主要海藻糖的糖脂,即海藻糖单核糖酸盐和海藻糖二元醇,其细胞壁脂质级分。结果表明,较少的海藻糖C.谷氨酰胺突变体的巨大改变的细胞壁脂质双层可能是在最小培养基中观察到这种菌株的观察到的生长缺乏。在这里报道的C.谷氨酸中海藻糖生物合成遗传和生理解剖结果的结果可能是对含氰酸的棒状细菌的整个系统发育基团的一般相关性。

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