4.7 Article

Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 62, Issue 13, Pages 4481-4493

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/err145

Keywords

Chloroplast ultrastructure; chlorophyll; cytochrome oxidase; glycolate oxidase; hydrogen sulphide (H2S); photosynthesis; ribulose-1; 5-bisphoshate carboxylase; Spinacia oleracea; thiol redox modification

Categories

Funding

  1. Natural Science Foundation of China (NSFC) [30930076]
  2. Foundation of the Chinese Ministry of Education [20070384033]
  3. Xiamen University
  4. Changjiang Scholarship
  5. Research Grant Council of the Hong Kong Special Administrative Region [465009, 465410]
  6. Chinese University of Hong Kong
  7. Division Of Integrative Organismal Systems
  8. Direct For Biological Sciences [848263] Funding Source: National Science Foundation

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Hydrogen sulphide (H2S) is emerging as a potential messenger molecule involved in modulation of physiological processes in animals and plants. In this report, the role of H2S in modulating photosynthesis of Spinacia oleracea seedlings was investigated. The main results are as follows. (i) NaHS, a donor of H2S, was found to increase the chlorophyll content in leaves. (ii) Seedlings treated with different concentrations of NaHS for 30 d exhibited a significant increase in seedling growth, soluble protein content, and photosynthesis in a dose-dependent manner, with 100 mu M NaHS being the optimal concentration. (iii) The number of grana lamellae stacking into the functional chloroplasts was also markedly increased by treatment with the optimal NaHS concentration. (iv) The light saturation point (Lsp), maximum net photosynthetic rate (Pmax), carboxylation efficiency (CE), and maximal photochemical efficiency of photosystem II (F-v/F-m) reached their maximal values, whereas the light compensation point (Lcp) and dark respiration (Rd) decreased significantly under the optimal NaHS concentration. (v) The activity of ribulose-1,5-bisphosphate carboxylase (RuBISCO) and the protein expression of the RuBISCO large subunit (RuBISCO LSU) were also significantly enhanced by NaHS. (vi) The total thiol content, glutathione and cysteine levels, internal concentration of H2S, and O-acetylserine(thiol)lyase and L-cysteine desulphydrase activities were increased to some extent, suggesting that NaHS also induced the activity of thiol redox modification. (vii) Further studies using quantitative real-time PCR showed that the gene encoding the RuBISCO large subunit (RBCL), small subunit (RBCS), ferredoxin thioredoxin reductase (FTR), ferredoxin (FRX), thioredoxin m (TRX-m), thioredoxin f (TRX-f), NADP-malate dehydrogenase (NADP-MDH), and O-acetylserine(thiol)lyase (OAS) were up-regulated, but genes encoding serine acetyltransferase (SERAT), glycolate oxidase (GYX), and cytochrome oxidase (CCO) were down-regulated after exposure to the optimal concentration of H2S. These findings suggest that increases in RuBISCO activity and the function of thiol redox modification may underlie the amelioration of photosynthesis and that H2S plays an important role in plant photosynthesis regulation by modulating the expression of genes involved in photosynthesis and thiol redox modification.

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