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麦角硫因的生物合成与代谢。耻垢分枝杆菌中麦角硫因生物合成与降解过程中潜在中间产物的细胞水平。

Mycothiol biosynthesis and metabolism. Cellular levels of potential intermediates in the biosynthesis and degradation of mycothiol in mycobacterium smegmatis.

作者信息

Anderberg S J, Newton G L, Fahey R C

机构信息

Department of Chemistry and Biochemistry, University of California at San Diego, La Jolla, California 92093-0506, USA.

出版信息

J Biol Chem. 1998 Nov 13;273(46):30391-7. doi: 10.1074/jbc.273.46.30391.

Abstract

Mycothiol (MSH; 1-D-myo-inosityl-2-(N-acetyl-L-cysteinyl)amido-2-deoxy-alpha-D- glucop yranoside (AcCys-GlcN-Ins)) is a novel thiol produced at millimolar levels by mycobacteria and other actinomycetes that do not make glutathione. We developed methods to determine the major components of MSH (AcCys, Cys-GlcN, AcCys-GlcN, Cys-GlcN-Ins, GlcN-Ins) in cell extracts. Mycobacterium smegmatis was shown to produce measurable levels (nmol/g of residual dry weight) of AcCys ( approximately 30), Cys-GlcN-Ins (approximately 8), and GlcN-Ins (approximately 100) but not Cys-GlcN (<3) or AcCys-GlcN (<80) during exponential growth in Middlebrook 7H9 medium. The level of GlcN-Ins declined 10-fold in stationary phase and approximately 5-fold in 7H9 medium lacking glucose. Incubation in 10 mM AcCys produced 50- and 1000-fold increases in cellular Cys and AcCys levels, respectively, a 10-fold decrease in GlcN-Ins and a transient 3-fold increase in Cys-GlcN-Ins. These results exclude Cys-GlcN and AcCys-GlcN as intermediates in MSH biosynthesis and implicate GlcN-Ins and Cys-GlcN-Ins as key intermediates. Assay of GlcN-Ins/ATP-dependent ligase activity with Cys and AcCys as substrates revealed that Cys was at least an order of magnitude better substrate. Based on the cellular measurements, MSH biosynthesis involves assembly of GlcN-Ins, ligation with Cys to produce Cys-GlcN-Ins, and acetylation of the latter to produce MSH.

摘要

巯基乙醇(MSH;1-D-肌醇-2-(N-乙酰-L-半胱氨酰)氨基-2-脱氧-α-D-葡萄糖苷(AcCys-GlcN-Ins))是一种由不产生谷胱甘肽的分枝杆菌和其他放线菌以毫摩尔水平产生的新型硫醇。我们开发了测定细胞提取物中MSH主要成分(AcCys、Cys-GlcN、AcCys-GlcN、Cys-GlcN-Ins、GlcN-Ins)的方法。耻垢分枝杆菌在Middlebrook 7H9培养基中指数生长期间,显示产生可测量水平(nmol/克残余干重)的AcCys(约30)、Cys-GlcN-Ins(约8)和GlcN-Ins(约100),但不产生Cys-GlcN(<3)或AcCys-GlcN(<80)。GlcN-Ins的水平在稳定期下降10倍,在缺乏葡萄糖的7H9培养基中下降约5倍。在10 mM AcCys中孵育分别使细胞内Cys和AcCys水平增加50倍和1000倍,GlcN-Ins下降10倍,Cys-GlcN-Ins短暂增加3倍。这些结果排除了Cys-GlcN和AcCys-GlcN作为MSH生物合成中间体的可能性,并暗示GlcN-Ins和Cys-GlcN-Ins是关键中间体。以Cys和AcCys为底物测定GlcN-Ins/ATP依赖性连接酶活性表明,Cys至少是一个数量级更好的底物。基于细胞测量结果,MSH生物合成涉及GlcN-Ins的组装、与Cys连接以产生Cys-GlcN-Ins,以及后者的乙酰化以产生MSH。

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