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Alginate formation in Azotobacter vinelandii UWD during stationary phase and the turnover of poly-β-hydroxybutyrate

机译:在静止阶段Zinotobacter vinelandii UWD中的藻酸盐形成及多β-羟基丁酸盐的营业额

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Azotobacter vinelandii UWD is a mutant of strain UW that is defective in the respiratory oxidation of NADH. This mutation causes an overproduction of polyhydroxyalkanoates (PHAs), as polyester synthesis is used as an alternative electron sink. Since PHAs have potential for use as natural, biodegradable plastics, studies of physiology related to their production are of interest. Alginate production by this strain is limited to 11?μg (mg cell protein)?1, which permits high efficiency conversion of carbon source into PHA. However, ≤400?μg (mg cell protein)?1 was formed when UWD cells were oxygen-limited and in the stationary phase of growth. Alginate formation was fuelled by PHA turnover, which was coincident with the synthesis of alkyl resorcinols, under conditions of exogenous glucose limitation. However, alginate production was a phenotypic and reversible change. Alginate production was stopped by interruption of algD with Tn5lacZ. LacZ activity in UWD was shown to increase in stationary phase, while LacZ activity in a similarly constructed mutant of strain UW did not. Transcription of algD in strain UWD started from a previously identified RpoD promoter and not from the AlgU (RpoE) promoter. This is because strain UWD has a natural insertion element in algU. Differences between strain UW and UWD may reside in the defective respiratory oxidation of NADH, where the NADH surplus in strain UWD may act as a signal of stationary phase. Indeed, a backcross of UW DNA into UWD generated NADH-oxidase-proficient cells that failed to form alginate in stationary phase. Evidence is also presented to show that the RpoD promoter may be recognized by the stationary phase sigma factor (RpoS), which may mediate alginate production in strain UWD.
机译:Azotobacter Vinelandii UWD是菌株uW的突变体,其在NADH的呼吸氧化中有缺陷。该突变导致多羟基烷烷酸盐(PHA)过量生产,因为聚酯合成用作替代电子汇。由于PHA具有作为天然的,可生物降解的塑料的潜力,因此与其生产有关的生理学的研究是感兴趣的。通过该菌株的藻酸盐产生限于<11?μg(mg细胞蛋白)α1,其允许碳源的高效转化为pHa。然而,当UWD细胞氧限制并且在生长的固定阶段时,形成≤400≤μg(mg细胞蛋白)α1。通过PHA转换来促进藻酸盐形成,在外源葡萄糖限制的条件下,通过合成烷基间苯二酚的合成重合。然而,海藻酸盐产量是一种表型和可逆的变化。通过用TN5LACZ中断藻类中断藻酸盐生产。 UWD中的LacZ活性显示出固定相增加,而LACZ活性在菌株的类似构建的突变体中没有。菌株在菌株UWD中的转录从先前鉴定的RPOD启动子开始,而不是来自Algu(RPoE)启动子。这是因为菌株UWD在Algu中具有自然插入元件。应变UW和UWD之间的差异可能存在于NADH的缺陷呼吸氧化中,其中应变UWD中的NADH剩余可以用作静止阶段的信号。实际上,将UW DNA的远程进入UWD产生的NADH-氧化酶易碎细胞,未在固定相中形成藻酸盐。还提出了证据表明RPOD启动子可以通过固定阶段Sigma因子(RPO)来识别,其可以在菌株UWD中介导藻酸盐产生。

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