4.8 Article

XTMS: pathway design in an eXTended metabolic space

期刊

NUCLEIC ACIDS RESEARCH
卷 42, 期 W1, 页码 W389-W394

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gku362

关键词

-

资金

  1. Genopole [ATIGE]
  2. Pole de Recherche et d'Enseignement Superieur (PRES) UniverSud Paris [PROMISENG]
  3. ab-SYNTH
  4. Agence Nationale de la Recherche (ANR) [Chair of Excellence]
  5. ANR

向作者/读者索取更多资源

As metabolic engineering and synthetic biology progress toward reaching the goal of a more sustainable use of biological resources, the need of increasing the number of value-added chemicals that can be produced in industrial organisms becomes more imperative. Exploring, however, the vast possibility of pathways amenable to engineering through heterologous genes expression in a chassis organism is complex and unattainable manually. Here, we present XTMS, a web-based pathway analysis platform available at http://xtms.issb.genopole.fr, which provides full access to the set of pathways that can be imported into a chassis organism such as Escherichia coli through the application of an Extended Metabolic Space modeling framework. The XTMS approach consists on determining the set of biochemical transformations that can potentially be processed in vivo as modeled by molecular signatures, a specific coding system for derivation of reaction rules for metabolic reactions and enumeration of all the corresponding substrates and products. Most promising routes are described in terms of metabolite exchange, maximum allowable pathway yield, toxicity and enzyme efficiency. By answering such critical design points, XTMS not only paves the road toward the rationalization of metabolic engineering, but also opens new processing possibilities for non-natural metabolites and novel enzymatic transformations.

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

4.8
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