earticle

논문검색

In silico experiments based on genome-scale metabolic model for biochemical production in Escherichia coli

초록

영어

There are too many combinatorial gene knock-out targets to achieve the overproduction of desired products. However, researchers cannot perform every single experiment to identify the best combination of gene knock-out targets. This is the reason that computational simulations can play important roles for the overproduction of desired products. Flux balance analysis (FBA) optimizes a specific objective function by linear programming. In order to incorporate the
physiological characteristics of the organisms under gene knock-out conditions, various methods such as MOMA and ROOM were developed. However, these algorithms optimize only the limited objective function. To improve a strain for biochemical production, the organism should be investigated from diverse sides simultaneously. In this respect, we propose a new approach called the flux scanning with compromised objective fluxes (FSCOF) that optimizes
multi-objective functions. [This work was supported by the Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MOST) (No. M10309020000-03B5002-00000). Further supports by LG Chem Chair Professorship, Microsoft and IBM SUR program are appreciated.]

저자정보

  • Jong Myoung Park Department of Chemical & Biomolecular Engineering (BK21 program)
  • Tae Yong Kim Department of Chemical & Biomolecular Engineering (BK21 program),
  • Sang Yup Lee Department of Chemical & Biomolecular Engineering (BK21 program), Department of BioSystems, BioProcess Engineering Research Center,and Bioinformatics Research Center, Korea Advanced Institute of Science and Technology

참고문헌

자료제공 : 네이버학술정보

    함께 이용한 논문

      ※ 원문제공기관과의 협약기간이 종료되어 열람이 제한될 수 있습니다.

      0개의 논문이 장바구니에 담겼습니다.