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首页> 外文期刊>Journal of bacteriology >Identification and Regulation of the N-Acetylglucosamine Utilization Pathway of the Plant Pathogenic Bacterium Xanthomonas campestris pv. campestris
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Identification and Regulation of the N-Acetylglucosamine Utilization Pathway of the Plant Pathogenic Bacterium Xanthomonas campestris pv. campestris

机译:植物病原细菌Xanthomonas campestris pv的N-乙酰氨基葡萄糖利用途径的鉴定和调控。桔梗

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Xanthomonas campestris pv. campestris, the causal agent of black rot disease of brassicas, is known for its ability to catabolize a wide range of plant compounds. This ability is correlated with the presence of specific carbohydrate utilization loci containing TonB-dependent transporters (CUT loci) devoted to scavenging specific carbohydrates. In this study, we demonstrate that there is an X. campestris pv. campestris CUT system involved in the import and catabolism of N-acetylglucosamine (GlcNAc). Expression of genes belonging to this GlcNAc CUT system is under the control of GlcNAc via the LacI family NagR and GntR family NagQ regulators. Analysis of the NagR and NagQ regulons confirmed that GlcNAc utilization involves NagA and NagB-II enzymes responsible for the conversion of GlcNAc-6-phosphate to fructose-6-phosphate. Mutants with mutations in the corresponding genes are sensitive to GlcNAc, as previously reported for Escherichia coli. This GlcNAc sensitivity and analysis of the NagQ and NagR regulons were used to dissect the X. campestris pv. campestris GlcNAc utilization pathway. This analysis revealed specific features, including the fact that uptake of GlcNAc through the inner membrane occurs via a major facilitator superfamily transporter and the fact that this amino sugar is phosphorylated by two proteins belonging to the glucokinase family, NagK-IIA and NagK-IIB. However, NagK-IIA seems to play a more important role in GlcNAc utilization than NagK-IIB under our experimental conditions. The X. campestris pv. campestris GlcNAc NagR regulon includes four genes encoding TonB-dependent active transporters (TBDTs). However, the results of transport experiments suggest that GlcNAc passively diffuses through the bacterial envelope, an observation that calls into question whether GlcNAc is a natural substrate for these TBDTs and consequently is the source of GlcNAc for this nonchitinolytic plant-associated bacterium.
机译: Xanthomonas campestris pv。芸苔属,芸苔属黑腐病的病因,以其分解代谢多种植物化合物的能力而闻名。该能力与特定的 c 糖化物 u 利用位点的存在相关,该位点包含专门用于清除特定碳水化合物的依赖于onB的转运蛋白(CUT位点)的 T 。在这项研究中,我们证明有一个 X。 Campestris pv。 Campestris CUT系统参与 N -乙酰氨基葡萄糖(GlcNAc)的导入和分解代谢。属于该GlcNAc CUT系统的基因的表达受LacI家族NagR和GntR家族NagQ调节剂的控制。 NagR和NagQ调节子的分析证实,GlcNAc的利用涉及NagA和NagB-II酶,这些酶负责将GlcNAc-6-磷酸转化为果糖-6-磷酸。如先前关于大肠杆菌的报道,在相应基因中具有突变的突变体对GlcNAc敏感。这种GlcNAc敏感性和NagQ和NagR调节子的分析被用于解剖 X。 Campestris pv。樟脑GlcNAc利用途径。该分析揭示了特定的特征,包括通过主要的促进子超家族转运蛋白通过内膜吸收GlcNAc的事实,以及该氨基糖被属于葡萄糖激酶家族的两种蛋白质NagK-IIA和NagK-IIB磷酸化的事实。但是,在我们的实验条件下,NagK-IIA在GlcNAc的利用中似乎比NagK-IIB发挥着更重要的作用。 X。 Campestris pv。 campestris GlcNAc NagR regulon包含编码TonB依赖性主动转运蛋白(TBDT)的四个基因。但是,运输实验的结果表明,GlcNAc被动扩散通过细菌包膜,这一观察结果令人质疑,GlcNAc是否是这些TBDT的天然底物,因此是该非壳多糖分解植物相关细菌的GlcNAc来源。

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