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海洋红杆菌属成员抑制海洋杆菌DSM 17395中的碳水化合物分解代谢。

Carbohydrate catabolism in Phaeobacter inhibens DSM 17395, a member of the marine roseobacter clade.

作者信息

Wiegmann Katharina, Hensler Michael, Wöhlbrand Lars, Ulbrich Marcus, Schomburg Dietmar, Rabus Ralf

出版信息

Appl Environ Microbiol. 2014 Aug;80(15):4725-37. doi: 10.1128/AEM.00719-14.

Abstract

Since genome analysis did not allow unambiguous reconstruction of transport, catabolism, and substrate-specific regulation for several important carbohydrates in Phaeobacter inhibens DSM 17395, proteomic and metabolomic analyses of N-acetylglucosamine-, mannitol-, sucrose-, glucose-, and xylose-grown cells were carried out to close this knowledge gap. These carbohydrates can pass through the outer membrane via porins identified in the outer membrane fraction. For transport across the cytoplasmic membrane, carbohydrate-specific ABC transport systems were identified. Their coding genes mostly colocalize with the respective "catabolic" and "regulatory" genes. The degradation of N-acetylglucosamine proceeds via N-acetylglucosamine-6-phosphate and glucosamine-6-phosphate directly to fructose-6-phosphate; two of the three enzymes involved were newly predicted and identified. Mannitol is catabolized via fructose, sucrose via fructose and glucose, glucose via glucose-6-phosphate, and xylose via xylulose-5-phosphate. Of the 30 proteins predicted to be involved in uptake, regulation, and degradation, 28 were identified by proteomics and 19 were assigned to their respective functions for the first time. The peripheral degradation pathways feed into the Entner-Doudoroff (ED) pathway, which is connected to the lower branch of the Embden-Meyerhof-Parnas (EMP) pathway. The enzyme constituents of these pathways displayed higher abundances in P. inhibens DSM 17395 cells grown with any of the five carbohydrates tested than in succinate-grown cells. Conversely, gluconeogenesis is turned on during succinate utilization. While tricarboxylic acid (TCA) cycle proteins remained mainly unchanged, the abundance profiles of their metabolites reflected the differing growth rates achieved with the different substrates tested. Homologs of the 74 genes involved in the reconstructed catabolic pathways and central metabolism are present in various Roseobacter clade members.

摘要

由于基因组分析无法明确重建抑制海洋杆菌DSM 17395中几种重要碳水化合物的转运、分解代谢和底物特异性调控过程,因此开展了对在N-乙酰葡糖胺、甘露醇、蔗糖、葡萄糖和木糖上生长的细胞的蛋白质组学和代谢组学分析,以填补这一知识空白。这些碳水化合物可通过在外膜组分中鉴定出的孔蛋白穿过外膜。对于跨细胞质膜的转运,鉴定出了碳水化合物特异性ABC转运系统。它们的编码基因大多与各自的“分解代谢”和“调控”基因共定位。N-乙酰葡糖胺的降解通过N-乙酰葡糖胺-6-磷酸和葡糖胺-6-磷酸直接进行至果糖-6-磷酸;所涉及的三种酶中有两种是新预测和鉴定的。甘露醇通过果糖进行分解代谢,蔗糖通过果糖和葡萄糖进行分解代谢,葡萄糖通过葡萄糖-6-磷酸进行分解代谢,木糖通过木酮糖-5-磷酸进行分解代谢。在预测参与摄取、调控和降解的30种蛋白质中,有28种通过蛋白质组学鉴定出来,其中19种首次被赋予各自的功能。外周降解途径汇入恩特纳-杜德洛夫(ED)途径,该途径与糖酵解(EMP)途径的下游分支相连。在以所测试的五种碳水化合物中的任何一种生长的抑制海洋杆菌DSM 17395细胞中,这些途径的酶成分显示出比在以琥珀酸盐生长的细胞中更高的丰度。相反,在琥珀酸盐利用期间糖异生被开启。虽然三羧酸(TCA)循环蛋白基本保持不变,但其代谢物的丰度谱反映了用不同测试底物实现的不同生长速率。参与重建的分解代谢途径和中心代谢的74个基因的同源物存在于各种红杆菌属分支成员中。

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