In silico analyses for elucidation of Escherichia coli physiology and its metabolic engineering applications = 대장균의 생리학적 특징 규명 및 대사공학적 응용을 위한 다양한 인실리코 분석

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Escherichia coli is the most widely considered prokaryotic model organism, and frequently used as the most important production host in the field of biotechnology. For better understanding of bacterial physiology and enhanced production of bio-chemicals that are of industrial values, plenty of omics data have been generated in recent years. In particular, genomic information of various E. coli strains has enabled reconstruction of their genome-scale metabolic models, which have constantly been updated. These metabolic models are used to better understand physiological features of E. coli and provide novel insights for metabolic engineering. Accordingly, in this thesis, genome-scale metabolic models for E. coli B REL606 and W strains were newly reconstructed based on comparative genome analyses, and these models were utilized for various in silico analyses. First, biomass formation rate and production capacities of industrially important organic acids were predicted using the constructed models of E. coli K-12, B REL606, and W strains. Also, iron ion ($Fe^{2+}$) effects observed as the specific physiological features of W strain were identified through comparative genome analyses and experimental validation. Next, because metabolic cofactors, including NADH and NADPH, contribute to significant roles in metabolic flux distributions, E. coli K-12 model was used to elucidate the redox cofactor states under various environmental and genetic perturbed conditions. Also, strategy of cofactor manipulations was developed for the enhanced production of desired products in this study. Finally, using large transcriptomic data and information of protein-DNA regulatory interactions, a comprehensive transcriptional regulatory network was constructed and integrated with the metabolic network of E. coli K-12. Subsequently, transcriptional factors (TFs) were systematically targeted for various applications of metabolic engineering because TFs can (in)directly control gene expressions throughout the microbial system. In conclusions, these studies provide important insights to physiological features of E. coli strains, and are expected to contribute to the advances of microbiology and metabolic engineering.
Advisors
Lee, Sang Yupresearcher이상엽researcher
Description
한국과학기술원 :생명화학공학과,
Publisher
한국과학기술원
Issue Date
2013
Identifier
325007
Language
eng
Description

학위논문(석사) - 한국과학기술원 : 생명화학공학과, 2013.8,[vii, 73 p. :]

Keywords

Escherichia coli▼agenome-scale metabolic model▼ametabolic engineering▼atranscriptional regulatory network▼ain silico analysis; 대장균▼a게놈 대사 모델▼a대사공학▼a전사조절네트워크▼a인실리코 분석

URI
http://hdl.handle.net/10203/266343
Link
http://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=848980&flag=dissertation
Appears in Collection
CBE-Theses_Master(석사논문)
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