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Chloroplastic ascorbate peroxidases targeted to stroma or thylakoid membrane: The chicken or egg dilemma
Author(s) -
JardimMesseder Douglas,
Zamocky Marcel,
SachettoMartins Gilberto,
MargisPinheiro Márcia
Publication year - 2022
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1002/1873-3468.14438
Subject(s) - thylakoid , peroxidase , biochemistry , biology , chloroplast , apx , chloroplast stroma , ascorbic acid , enzyme , gene , food science
Ascorbate peroxidases (APXs) are heme peroxidases that remove hydrogen peroxide in different subcellular compartments with concomitant ascorbate cycling. Here, we analysed and discussed phylogenetic and molecular features of the APX family. Ancient APX originated as a soluble stromal enzyme, and early during plant evolution, acquired both chloroplast‐targeting and mitochondrion‐targeting sequences and an alternative splicing mechanism whereby it could be expressed as a soluble or thylakoid membrane‐bound enzyme. Later, independent duplication and neofunctionalization events in some angiosperm groups resulted in individual genes encoding stromal, thylakoidal and mitochondrial isoforms. These data reaffirm the complexity of plant antioxidant defenses that allow diverse plant species to acquire new means to adapt to changing environmental conditions.