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S-肌苷-L-高半胱氨酸水解酶,一种参与S-腺苷-L-甲硫氨酸循环的新型酶。

S-Inosyl-L-Homocysteine Hydrolase, a Novel Enzyme Involved in S-Adenosyl-L-Methionine Recycling.

作者信息

Miller Danielle, Xu Huimin, White Robert H

机构信息

Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA.

Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA

出版信息

J Bacteriol. 2015 Jul;197(14):2284-91. doi: 10.1128/JB.00080-15. Epub 2015 Apr 27.

Abstract

UNLABELLED

S-Adenosyl-L-homocysteine, the product of S-adenosyl-L-methionine (SAM) methyltransferases, is known to be a strong feedback inhibitor of these enzymes. A hydrolase specific for S-adenosyl-L-homocysteine produces L-homocysteine, which is remethylated to methionine and can be used to regenerate SAM. Here, we show that the annotated S-adenosyl-L-homocysteine hydrolase in Methanocaldococcus jannaschii is specific for the hydrolysis and synthesis of S-inosyl-L-homocysteine, not S-adenosyl-L-homocysteine. This is the first report of an enzyme specific for S-inosyl-L-homocysteine. As with S-adenosyl-L-homocysteine hydrolase, which shares greater than 45% sequence identity with the M. jannaschii homologue, the M. jannaschii enzyme was found to copurify with bound NAD(+) and has Km values of 0.64 ± 0.4 mM, 0.0054 ± 0.006 mM, and 0.22 ± 0.11 mM for inosine, L-homocysteine, and S-inosyl-L-homocysteine, respectively. No enzymatic activity was detected with S-adenosyl-L-homocysteine as the substrate in either the synthesis or hydrolysis direction. These results prompted us to redesignate the M. jannaschii enzyme an S-inosyl-L-homocysteine hydrolase (SIHH). Identification of SIHH demonstrates a modified pathway in this methanogen for the regeneration of SAM from S-adenosyl-L-homocysteine that uses the deamination of S-adenosyl-L-homocysteine to form S-inosyl-L-homocysteine.

IMPORTANCE

In strictly anaerobic methanogenic archaea, such as Methanocaldococcus jannaschii, canonical metabolic pathways are often not present, and instead, unique pathways that are deeply rooted on the phylogenetic tree are utilized by the organisms. Here, we discuss the recycling pathway for S-adenosyl-L-homocysteine, produced from S-adenosyl-L-methionine (SAM)-dependent methylation reactions, which uses a hydrolase specific for S-inosyl-L-homocysteine, an uncommon metabolite. Identification of the pathways and the enzymes involved in the unique pathways in the methanogens will provide insight into the biochemical reactions that were occurring when life originated.

摘要

未标记

S-腺苷-L-高半胱氨酸是S-腺苷-L-甲硫氨酸(SAM)甲基转移酶的产物,已知是这些酶的一种强反馈抑制剂。一种对S-腺苷-L-高半胱氨酸具有特异性的水解酶产生L-高半胱氨酸,L-高半胱氨酸再甲基化生成甲硫氨酸,可用于再生SAM。在此,我们表明,詹氏甲烷球菌中注释的S-腺苷-L-高半胱氨酸水解酶对S-肌苷-L-高半胱氨酸的水解和合成具有特异性,而非对S-腺苷-L-高半胱氨酸。这是关于一种对S-肌苷-L-高半胱氨酸具有特异性的酶的首次报道。与与詹氏甲烷球菌同源物具有大于45%序列同一性的S-腺苷-L-高半胱氨酸水解酶一样,发现詹氏甲烷球菌的这种酶与结合的NAD(+)共纯化,并且对肌苷、L-高半胱氨酸和S-肌苷-L-高半胱氨酸的Km值分别为0.64±0.4 mM、0.0054±0.006 mM和0.22±0.11 mM。在合成或水解方向上,以S-腺苷-L-高半胱氨酸为底物均未检测到酶活性。这些结果促使我们将詹氏甲烷球菌的这种酶重新命名为S-肌苷-L-高半胱氨酸水解酶(SIHH)。SIHH的鉴定证明了这种产甲烷菌中从S-腺苷-L-高半胱氨酸再生SAM的一条修饰途径,该途径利用S-腺苷-L-高半胱氨酸脱氨形成S-肌苷-L-高半胱氨酸。

重要性

在严格厌氧的产甲烷古菌中,如詹氏甲烷球菌,典型的代谢途径通常不存在,相反,生物体利用深深植根于系统发育树的独特途径。在此,我们讨论了由依赖S-腺苷-L-甲硫氨酸(SAM)的甲基化反应产生的S-腺苷-L-高半胱氨酸的循环途径,该途径使用一种对S-肌苷-L-高半胱氨酸具有特异性的水解酶,S-肌苷-L-高半胱氨酸是一种不常见的代谢物。鉴定产甲烷菌中独特途径所涉及的途径和酶将为生命起源时发生的生化反应提供见解。

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