Abstract

Previously, Chlorella pyrenoidosa strain IOAC707S was found to produce hydrogen under nitrogen deprivation in seawater medium, without dark incubation, N2 flushing or addition of uncoupler, which made it a candidate for clean and renewable energy production. To understand the molecular mechanism underlying hydrogen production by C. pyrenoidosa under nitrogen deprivation, iTRAQ-based proteomic analysis was conducted to investigate the differences in protein abundance under nitrogen deprivation (L1-N) compared with the control (CK). In total, 119 KEGG pathways were mapped for 2383 proteins, among which, the expression levels of most proteins involved in chlorophyll synthesis were down-regulated, while those involved in chlorophyll degradation were up-regulated in the L1-N culture; the expression level of serine glyoxylate aminotransferase involved in photorespiration was up-regulated 1.25 fold in the L1-N culture at 44 h, and the expression levels of most proteins involved in mitochondrial respiration were up-regulated in the L1-N culture. These results indicated a decrease of chlorophyll and an increase of respiration, which favored the establishment of anaerobiosis and hydrogen production.

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