Renewable biohydrogen production from Clostridium sp. LQ25 using different forms of ferric as electron acceptor

Clostridium sp. LQ25 was cultured in different forms of ferric (ferric citrate and ferric hydroxide) as electron acceptors to investigate growth, ferric reduction, hydrogen production, fermentation products and fermentation process. The growth of the strain LQ25 detected by protein was 82.8 +/- 2.1 mg/L and 73.5 +/- 1.7 mg/L using ferric citrate and ferric hydroxide as electron acceptors, which was 33.3 % and 18.4 % higher than without ferric, respectively. The accumulation concentration of Fe(II) was 9.0 +/- 0.6 mg/L and 5.0 +/- 0.2 mg/L when using ferric citrate and ferric hydroxide as electron acceptors, and ferric citrate was 1.8-fold higher than ferric hydroxide, which indicated that the ability of ferric reduction was higher using ferric citrate as electron acceptor. The hydrogen production of strain LQ25 was 238.0 +/- 1.0 mmol/mol glucose and 113.0 +/- 1.3 mmol/mol glucose under condition of ferric citrate and ferric hydroxide as electron acceptors, which was 2.6 and 1.2-fold higher than without ferric, respectively. The growth and hydrogen production of strain LQ25 was promoted by using ferric as electron acceptor, while the fermentation type of strain did not change and was always butyrate type. The differential expression of the genes of strain LQ25 was significant when using ferric as electron acceptor, mainly in NADH and PFL pathway. This study provided preliminary evidence for hydrogen production by Clostridium sp. LQ25 in the presence of electron acceptor.

Automated summary

This study investigates the growth, ferric reduction, hydrogen production, fermentation products, and fermentation process of Clostridium sp. LQ25 cultured using different forms of ferric as electron acceptors. The results show that the use of ferric as electron acceptor promotes the growth and hydrogen production of strain LQ25 while the fermentation type remains unchanged.