Genome-Wide Analysis of Sugar Transporters Identifies the gtsA Gene for Glucose Transportation in Pseudomonas stutzeri A1501
文献类型: 外文期刊
第一作者: Liu, Yaqun
作者: Liu, Yaqun;Liu, Zhu;Liu, Yaqun;Shang, Liguo;Zhan, Yuhua;Lin, Min;Yan, Yongliang
作者机构:
关键词: Pseudomonas stutzeri A1501; sugar-transport system; glucose; gtsA gene; biological nitrogen fixation
期刊名称:MICROORGANISMS ( 影响因子:4.128; )
ISSN:
年卷期: 2020 年 8 卷 4 期
页码:
收录情况: SCI
摘要: Pseudomonas stutzeri A1501 possesses an extraordinary number of transporters which confer this rhizosphere bacterium with the sophisticated ability to metabolize various carbon sources. However, sugars are not a preferred carbon source for P. stutzeri A1501. The P. stutzeri A1501 genome has been sequenced, allowing for the homology-based in silico identification of genes potentially encoding sugar-transport systems by using established microbial sugar transporters as a template sequence. Genomic analysis revealed that there were 10 sugar transporters in P. stutzeri A1501, most of which belong to the ATP-binding cassette (ABC) family (5/10); the others belong to the phosphotransferase system (PTS), major intrinsic protein (MIP) family, major facilitator superfamily (MFS) and the sodium solute superfamily (SSS). These systems might serve for the import of glucose, galactose, fructose and other types of sugar. Growth analysis showed that the only effective medium was glucose and its corresponding metabolic system was relatively complete. Notably, the loci of glucose metabolism regulatory systems HexR, GltR/GtrS, and GntR were adjacent to the transporters ABC(MalEFGK), ABC(GtsABCD), and ABC(MtlEFGK), respectively. Only the ABC(GtsABCD) expression was significantly upregulated under both glucose-sufficient and -limited conditions. The predicted structure and mutant phenotype data of the key protein GtsA provided biochemical evidence that P. stutzeri A1501 predominantly utilized the ABC(GtsABCD) transporter for glucose uptake. We speculate that gene absence and gene diversity in P. stutzeri A1501 was caused by sugar-deficient environmental factors and hope that this report can provide guidance for further analysis of similar bacterial lifestyles.
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