4.8 Article

Homologous overexpression of hydrogenase and glycerol dehydrogenase in Clostridium pasteurianum to enhance hydrogen production from crude glycerol

Journal

BIORESOURCE TECHNOLOGY
Volume 284, Issue -, Pages 168-177

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2019.03.074

Keywords

Biohydrogen; Crude glycerol; Clostridium pasteurianum; Overexpression

Funding

  1. Department of Biotechnology, India
  2. British Council, United Kingdom [BT/IN/UK/DBT-BC/2015-16]
  3. BBSRC [BB/L013940/1] Funding Source: UKRI

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This study reports engineering of a hypertransformable variant of C. pasteurianum for bioconversion of glycerol into hydrogen (H-2). A functional glycerol-triggered hydrogen pathway was engineered based on two approaches: (1) increasing product yield by overexpression of immediate enzyme catalyzing H-2 production, (2) increasing substrate uptake by overexpression of enzymes involved in glycerol utilization. The first strategy aimed at overexpression of hydA gene encoding hydrogenase, and the second one, through combination of overexpression of dhaD1 and dhaK genes encoding glycerol dehydrogenase and dihydroxyacetone kinase. These genetic manipulations resulted in two recombinant strains (hydA(++)/dhaD1K(++) ) capable of producing 97% H-2 (v/v), with yields of 1.1 mol H-2/mol glycerol in hydA overexpressed strain, and 0.93 mol H-2 /mol glycerol in dhaD1K overexpressed strain, which was 1.5 fold higher than wild type. Among two strains, dhaD1K(++) consumed more glycerol than hydA(++) which proves that overexpression of glycerol enzymes has enhanced glycerol intake rate.

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