4.5 Article

In vitro activation of NAD-dependent alcohol dehydrogenases by Nudix hydrolases is more widespread than assumed

期刊

FEBS LETTERS
卷 588, 期 17, 页码 2993-2999

出版社

WILEY
DOI: 10.1016/j.febslet.2014.06.008

关键词

Methylotrophy; Alcohol dehydrogenase; Bacillus methanolicus

资金

  1. European Science Foundation (ESF) - SNF [09-EuroSYNBIO-FP-023, 31SY30-131039]
  2. EU-FP7 PROMYSE Products from Methanol by Synthetic Cell Factories
  3. Swiss National Science Foundation (SNF) [31SY30-131039] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

In the Gram-positive methylotroph Bacillus methanolicus, methanol oxidation is catalyzed by an NAD-dependent methanol dehydrogenase (Mdh) that belongs to the type III alcohol dehydrogenase (Adh) family. It was previously shown that the in vitro activity of B. methanolicus Mdh is increased by the endogenous activator protein Act, a Nudix hydrolase. Here we show that this feature is not unique, but more widespread among type III Adhs in combination with Act or other Act-like Nudix hydrolases. In addition, we studied the effect of site directed mutations in the predicted active site of Mdh and two other type III Adhs with regard to activity and activation by Act. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据