首页> 美国卫生研究院文献>Metabolites >Intracellular Fate of Universally Labelled 13C Isotopic Tracers of Glucose and Xylose in Central Metabolic Pathways of Xanthomonas oryzae
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Intracellular Fate of Universally Labelled 13C Isotopic Tracers of Glucose and Xylose in Central Metabolic Pathways of Xanthomonas oryzae

机译:普遍标记的米黄单胞菌中央代谢途径中葡萄糖和木糖的13 C同位素示踪剂的细胞内命运。

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摘要

The goal of this study is to map the metabolic pathways of poorly understood bacterial phytopathogen, Xanthomonas oryzae (Xoo) BXO43 fed with plant mimicking media XOM2 containing glutamate, methionine and either 40% [13C5] xylose or 40% [13C6] glucose. The metabolic networks mapped using the KEGG mapper and the mass isotopomer fragments of proteinogenic amino acids derived from GC-MS provided insights into the activities of Xoo central metabolic pathways. The average 13C in histidine, aspartate and other amino acids confirmed the activities of PPP, the TCA cycle and amino acid biosynthetic routes, respectively. The similar labelling patterns of amino acids (His, Ala, Ser, Val and Gly) from glucose and xylose feeding experiments suggests that PPP would be the main metabolic route in Xoo. Owing to the lack of annotated gene phosphoglucoisomerase in BXO43, the 13C incorporation in alanine could not be attributed to the competing pathways and hence warrants additional positional labelling experiments. The negligible presence of 13C incorporation in methionine brings into question its potential role in metabolism and pathogenicity. The extent of the average 13C labelling in several amino acids highlighted the contribution of pre-existing pools that need to be accounted for in 13C-flux analysis studies. This study provided the first qualitative insights into central carbon metabolic pathway activities in Xoo.
机译:这项研究的目的是绘制营养不良的细菌性植物病原体,米氏黄单胞菌(Xoo)BXO43的代谢途径,该植物饲喂含有植物模拟培养基XOM2的谷氨酸,蛋氨酸和40%[ 13 C5]木糖或40%的[ 13 C6]葡萄糖。使用KEGG作图仪绘制的代谢网络和源自GC-MS的蛋白原氨基酸的质量同位素异构体片段为Xoo中心代谢途径的活性提供了见识。组氨酸,天门冬氨酸和其他氨基酸的平均 13 C分别证实了PPP的活性,TCA循环和氨基酸的生物合成途径。来自葡萄糖和木糖喂养实验的氨基酸(His,Ala,Ser,Val和Gly)的相似标记模式表明PPP将成为Xoo的主要代谢途径。由于BXO43中缺少注释基因磷酸葡糖异构酶,丙氨酸中的 13 C掺入不能归因于竞争途径,因此有必要进行附加的位置标记实验。蛋氨酸中 13 C掺入量微不足道,使人们怀疑其在代谢和致病性中的潜在作用。几种氨基酸中平均 13 C标记的程度突出了 13 C-通量分析研究中需要考虑的现有池的贡献。这项研究为Xoo的中央碳代谢途径活动提供了第一个定性见解。

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