4.7 Article

New insights into chlorophyll-WSCP (water-soluble chlorophyll proteins) interactions : The case study of BnD22 (Brassica napus drought-induced 22 kDa)

期刊

PLANT PHYSIOLOGY AND BIOCHEMISTRY
卷 181, 期 -, 页码 71-80

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.plaphy.2022.03.023

关键词

Chl binding constants; Photobleaching; Microscale thermophoresis

资金

  1. national collaborative project entitled RAPSODYN - program Investments for the Future [ANR-11-BTBR-0004]
  2. French Research Ministry (MESR, Ministere de l'Enseignement Superieur et de la Recherche)
  3. Brittany regional authority
  4. Agence Nationale de la Recherche (ANR) [ANR-11-BTBR-0004] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

This study presents a novel method for assessing chlorophyll binding to water-soluble chlorophyll-proteins (WSCPs) and investigates the binding characteristics and protective effects of a WSCP protein BnD22. The results indicate that BnD22 has high affinity binding to chlorophylls and strong selectivity for Chla.
The water-soluble chlorophyll-proteins (WSCP) of class II from Brassicaceae are non-photosynthetic proteins that bind chlorophylls (Chls) and chlorophyll derivatives. Their physiological roles, biochemical functions and mode of action are still unclear. It is assumed that the WSCPs have a protection function against Chl photodamage during stressful conditions. WSCPs are subdivided into class IIA and class IIB according to their apparent Chla/b binding ratio. Although their Chla/Chlb binding selectivity has been partly characterized, their Chl affinities are not yet precisely defined. For instance, WSCPs IIA do not show any Chl binding preference while WSCPs IIB have greater affinity to Chlb. In this study, we present a novel method for assessment of Chl binding to WSCPs based on the differences of Chl photobleaching rates in a large range of Chl/protein ratios. The protein we have chosen to study WSCP is BnD22, a WSCP IIA induced in the leaves of Brassica napus under water deficit. BnD22 formed oligomeric complexes upon binding to Chla and/or Chlb allowing a protective effect against photodamage. The binding constants indicate that BnD22 binds with high affinity the Chls and with a strong selectivity to Chla. Moreover, dependending of Chl/protein ratio upon reconstitution, two distinct binding events were detected resulting from difference of Chl stoichiometry inside oligomeric complexes.

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