alexa
Reach Us +441414719275
Reconstruction Of Metabolic Networks From In Silico Labeled Substrates | 9347
ISSN: 0974-7230

Journal of Computer Science & Systems Biology
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Reconstruction of metabolic networks from in silico labeled substrates

International Conference on Integrative Biology Summit

Noushin Hadadi

ScientificTracks Abstracts: J Comput Sci Syst Biol

DOI: 10.4172/0974-7230.S1.002

Abstract
Metabolism transforms compounds to produce energy and building blocks. Metabolic network reconstruction allows better understanding of the metabolism and the catabolism of living cells and is commonly available at the metabolite level. Atom-level representation of the pathways could yield many insights into the exact mechanisms of enzymatic reactions. The ability to trace the fate of individual atoms through the metabolic pathways will also be very useful in many applications of metabolic engineering, systems biology and drug discovery. So far, the atom mappings in enzymatic reactions have not been studied in depth and most of the metabolic databases do not contain comprehensive information on atom tracing through biochemical pathways. KEGG RPAIR database contains such information between single metabolite pairs; however, it would be difficult to extend these mappings for every pathway and in every organism.We developed a computational framework for the in silico atom labeling and tracking through metabolic pathways. This framework analyzes all atom transitions based on enzymatic reaction rules by tracking the movement of every single atom through metabolic pathways. Our method allows a straightforward and computationally efficient means for the observation of all possible fluxes in a proposed network model based on atom biotransformation. We demonstrate the usefulness of our framework through a case study of biosynthesis of 3-Hydroxypropanoate (3HP) in E, coli and we compare the efficiency of different pathways in terms of the fate of the labeled atoms of substrates.
Biography
Noushin Hadadi is currently a Ph.D. student and research assistant in the group of Professor Vassily Hatzimanikatis at the Laboratory of Computational Systems Biotechnology (LCSB) at EPFL. Noushin earned her B.Sc. in Chemical Engineering at University of Tehran, Iran, in 2007. In 2008, Noushin joined EPFL as a Master student. She received her Master?s degree in Biochemical Engineering in 2011, and started her Ph.D. right afterwards. Her research interests include the development of computational frameworks for better understanding the metabolic networks of model organisms such as E, coli. Having full description of enzymatic reactions in metabolic networks helps for the discovery of novel metabolic pathways for the microbial production of valuable chemicals.
Relevant Topics
Top