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In silico identification of gene targets for bioethanol production from lignocellulosic hydrolysates using E. coli
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Metabolomics:Open Access

ISSN: 2153-0769

Open Access

In silico identification of gene targets for bioethanol production from lignocellulosic hydrolysates using E. coli


4th International Conference and Exhibition on Metabolomics & Systems Biology

April 27-29, 2015 Philadelphia, USA

Shireesh Srivastava

Scientific Tracks Abstracts: Metabolomics

Abstract :

Hydrolysates of lignocellulosic biomass contain both hexoses and pentoses, with pentoses contributing to about 30% of the fermentable sugars. Thus, it is important to select an organism that can utilize both sugars effectively. E. coli has the advantage that it can utilize pentose and hexose sugars. However, in the course of its fermentation, it produces many byproducts in addition to ethanol, such as acetate and formate. For efficient production of lignocellulosic biofuel, it is important to maximize product yield and minimize by-products formation. We employed in silico analyses on a recent genome-scale metabolic model of E. coli (iJO1366), to identify the knock-out targets to improve production of ethanol from glucose and xylose. Genetic Design through Local Search (GDLS) was employed to identify knock-out targets. GDLS involves reduction of the metabolic model to yield an equivalent Flux Balance Analysis model with fewer reactions and metabolites, followed by local search methodology to efficiently cover the space of genetic manipulations. Interestingly, similar knock-outs were identified for both glucose and xylose. Using these knock-outs, the ethanol was predicted to be over-90% of the theoretical yield on both glucose and xylose. The flux distribution in the mutant strain was identified through the Relative Change (RELATCH) method using available 13C-metabolic flux analysis data. The mutant strain had increased activity of Entner-Duodoroff pathway but reduced pentose-phosphate pathway and TCA cycle activity.

Biography :

Shireesh Srivastava has completed his PhD from Michigan State University and Postdoctoral studies from National Institute on Alcohol Abuse and Alcoholism, (NIAAA/NIH), Rockville, MD. He is a Team Leader in the DBT-ICGEB Center for Advanced Bioenergy Research, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India. He has published more than 15 papers in reputed journals and has won Fellows Award for Research Excellence at NIH as well as Sigma Xi award for excellence in graduate studies. His research interest is in metabolism and systems biology applications to solve challenging biomedical and biotechnological problems.

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