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首页> 外文期刊>Proteomics >Cell-cell communication in sourdough lactic acid bacteria: A proteomic study in Lactobacillus sanfranciscensis CB1
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Cell-cell communication in sourdough lactic acid bacteria: A proteomic study in Lactobacillus sanfranciscensis CB1

机译:发酵乳酸菌中的细胞间通讯:Sanfranciscensis乳杆菌CB1中的蛋白质组学研究

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摘要

The mechanisms of cell-cell communication in Lactobacillus sanfranciscensis CB1 were studied. The highest number of dead/damaged cells of L. sanfranciscensis CB1 was found in cocultures with Lactobacillus plantarum DC400 or Lactobacillus brevis CR13 when the late stationary phase of growth (18 h) was reached. 2-DE analysis was carried out. Almost the same proteins were induced in all three cocultures at the mid-exponential phase of growth (7 h). The number of induced proteins markedly increased at 18 h, especially when L. sanfranciscensis CB1 was cocultured with L. plantarum DC400 or L. brevis CR13. Nineteen overexpressed proteins were identified. These proteins had a central role in stress response mechanisms and LuxS-mediated signalling was involved in the regulation of most of them. The luxS and metF genes were partially sequenced in L. sanfranciscensis CB1. RT-PCR showed that the expression of luxS gene decreased from 7 to 12 h. It was highest in cocultures with L. plantarum DC400 and L. brevis CR13. 2(3H)dihydrofuranone-5ethyl and 2(3H)dihydrofuranone-5pentyl were identified as presumptive signalling molecules when L. sanfranciscensis CB1 was cocultured with L. brevis CR13 and, especially, L. plantarum DC400. The synthesis of other volatile compounds and peptidase activities were also influenced by the type of microbial cocultures.
机译:研究了旧金山乳杆菌CB1中细胞间通讯的机制。当达到生长的静止后期(18小时)时,与植物乳杆菌DC400或短乳杆菌CR13共培养时,发现了桑弗朗西斯菌CB1死亡/损坏的细胞数量最多。进行了2-DE分析。在生长的指数中期(7 h),在所有三种共培养物中几乎诱导了相同的蛋白质。诱导蛋白的数量在18 h明显增加,尤其是当Sanfranciscensis CB1与L. plantarum DC400或L. brevis CR13共培养时。鉴定出十九种过表达的蛋白质。这些蛋白质在应激反应机制中起着核心作用,LuxS介导的信号传导参与了大多数蛋白质的调控。 luxS和metF基因在L. sanfranciscensis CB1中部分测序。 RT-PCR结果表明,luxS基因的表达从7h降低到12h。在与植物乳杆菌DC400和短乳杆菌CR13的共培养物中,它最高。当将短链乳杆菌CB1与短乳杆菌CR13,尤其是植物乳杆菌DC400共培养时,将2(3H)二氢呋喃酮-5乙基和2(3H)二氢呋喃酮-5戊基鉴定为推测的信号分子。其他挥发性化合物的合成和肽酶活性也受到微生物共培养物类型的影响。

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