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Rediverting carbon flux in Clostridium ljungdahlii using CRISPR interference (CRISPRi).
Woolston, Benjamin M; Emerson, David F; Currie, Devin H; Stephanopoulos, Gregory.
Afiliação
  • Woolston BM; Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, MIT 56-469 C, Cambridge, MA 02139, United States.
  • Emerson DF; Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, MIT 56-469 C, Cambridge, MA 02139, United States.
  • Currie DH; Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, MIT 56-469 C, Cambridge, MA 02139, United States.
  • Stephanopoulos G; Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, MIT 56-469 C, Cambridge, MA 02139, United States. Electronic address: gregstep@mit.edu.
Metab Eng ; 48: 243-253, 2018 07.
Article em En | MEDLINE | ID: mdl-29906505
ABSTRACT
Clostridium ljungdahlii has emerged as an attractive candidate for the bioconversion of synthesis gas (CO, CO2, H2) to a variety of fuels and chemicals through the Wood-Ljungdahl pathway. However, metabolic engineering and pathway elucidation in this microbe is limited by the lack of genetic tools to downregulate target genes. To overcome this obstacle, here we developed an inducible CRISPR interference (CRISPRi) system for C. ljungdahlii that enables efficient (> 94%) transcriptional repression of several target genes, both individually and in tandem. We then applied CRISPRi in a strain engineered for 3-hydroxybutyrate (3HB) production to examine targets for increasing carbon flux toward the desired product. Downregulating phosphotransacetylase (pta) with a single sgRNA led to a 97% decrease in enzyme activity and a 2.3-fold increase in titer during heterotrophic growth. However, acetate production still accounted for 40% of the carbon flux. Repression of aldehydeferredoxin oxidoreductase (aor2), another potential route for acetate production, led to a 5% reduction in acetate flux, whereas using an additional sgRNA targeted to pta reduced the enzyme activity to 0.7% of the wild-type level, and further reduced acetate production to 25% of the carbon flux with an accompanying increase in 3HB titer and yield. These results demonstrate the utility of CRISPRi for elucidating and controlling carbon flow in C. ljungdahlii.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbono / Clostridium / Ácido 3-Hidroxibutírico / Engenharia Metabólica / Sistemas CRISPR-Cas Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carbono / Clostridium / Ácido 3-Hidroxibutírico / Engenharia Metabólica / Sistemas CRISPR-Cas Idioma: En Ano de publicação: 2018 Tipo de documento: Article