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Mechanisms of enhanced bio-H2 production in Ethanoligenens harbinense by L-cysteine supplementation: Analyses at growth and gene transcription levels

  • Xin Zhao
  • , Sicen Ye
  • , Nan Qi
  • , Xuejie Li
  • , Nisha Bao
  • , Defeng Xing*
  • , Nanqi Ren
  • *Corresponding author for this work
  • Northeastern University China
  • School of Environment, Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Bio-H2, produced from lignocellulosic biomass or organic wastewater, is an ideal future energy candidate due to its feature of renewability and sustainability. In order to uncover the mechanisms of the reducing agent of L-cysteine in bio-H2 production process, effects of L-cysteine on oxidation–reduction potential (ORP), cell growth, H2 yield by Ethanoligenens harbinense were investigated. Meanwhile, effects of L-cysteine on the expression of genes such as [FeFe]-hydrogenase (hydA), acetate kinase (AK), alcohol dehydrogenase (ADH), and lactate dehydrogenase (LDH) were analysed by quantitative reverse transcription PCR (qRT-PCR). The maximum H2 yield of 1.88 mol-H2/mol-glucose and dry cell weight of 0.92 g/L, which were about 1.57 and 1.51 folds of that of negative control, were obtained with supplementation of 800 mg/L L-cysteine. The experimental results indicated that the supplementation of L-cysteine at a suitable dosage (<800 mg/L) can enhances the H2 production by E. harbinense. The underlying mechanisms include decreasing ORP, promoting cell growth, and stimulating expression of key functional genes (hydA, AK, and ADH) involved in H2 production, together promoted the H2 release and enhanced the H2 production rate.

Original languageEnglish
Pages (from-to)143-147
Number of pages5
JournalFuel
Volume252
DOIs
StatePublished - 15 Sep 2019
Externally publishedYes

Keywords

  • Biohydrogen
  • Ethanoligenens harbinense
  • L-cysteine supplementation
  • hydrogenase
  • qRT-PCR

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