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Designing intracellular metabolism for production of target compounds by introducing a heterologous metabolic reaction based on a Synechosystis sp. 6803 genome-scale model

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바이오화학분류
    • 바이오플라스틱
      1. 고무
      2. 플라스틱
    • 바이오정밀화학
      1. 용매
      2. 화학제품
    • 화장품용 기능성소재
      1. 계면활성제⁄증점제
    • 의료용 화학소재
      1. 식품첨가제
논문

Designing intracellular metabolism for production of target compounds by introducing a heterologous metabolic reaction based on a Synechosystis sp. 6803 genome-scale model

학술지

Microbial cell factories

저자명

Shirai, Tomokazu; Osanai, Takashi; Kondo, Akihiko

초록

<P><B>Background</B></P><P>Designing optimal intracellular metabolism is essential for using microorganisms to produce useful compounds. Computerized calculations for flux balance analysis utilizing a genome-scale model have been performed for such designs. Many genome-scale models have been developed for different microorganisms. However, optimal designs of intracellular metabolism aimed at producing a useful compound often utilize metabolic reactions of only the host microbial cells. In the present study, we added reactions other than the metabolic reactions with <I>Synechosystis</I> sp. 6803 as a host to its genome-scale model, and constructed a metabolic model of hybrid cells (SyHyMeP) using computerized analysis. Using this model provided a metabolic design that improves the theoretical yield of succinic acid, which is a useful compound.</P><P><B>Results</B></P><P>Constructing the SyHyMeP model enabled new metabolic designs for producing useful compounds. In the present study, we developed a metabolic design that allowed for improved theoretical yield in the production of succinic acid during glycogen metabolism by <I>Synechosystis</I> sp. 6803. The theoretical yield of succinic acid production using a genome-scale model of these cells was 1.00&nbsp;mol/mol-glucose, but use of the SyHyMeP model enabled a metabolic design with which a 33&nbsp;% increase in theoretical yield is expected due to the introduction of isocitrate lyase, adding activations of endogenous tree reactions via D-glycerate in <I>Synechosystis</I> sp. 6803.</P><P><B>Conclusions</B></P><P>The SyHyMeP model developed in this study has provided a new metabolic design that is not restricted only to the metabolic reactions of individual microbial cells. The concept of construction of this model requires only replacement of the genome-scale model of the host microbial cells and can thus be applied to various useful microorganisms for metabolic design to produce compounds.</P><P><B>Electronic supplementary material</B></P><P>The online version of this article (doi:10.1186/s12934-016-0416-8) contains supplementary material, which is available to authorized users.</P>

발행연도

2016

발행기관

BioMed Central

라이선스

cc-by

ISSN

1475-2859

15

페이지

pp.13

주제어

Genome scale model; Flux balance analysis; Hybrid Metabolic Pathway design (HyMeP); Synechosystis sp. 6803; Succinate production

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1 2023-12-11

논문; 2016-01-18

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