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cpFBPaseII, a novel redox-independent chloroplastic isoform of fructose-1,6-bisphosphatase
- SERRATO, ANTONIO JESÚS, YUBERO-SERRANO, ELENA MARÍA, SANDALIO, LUISA MARÍA, MUÑOZ-BLANCO, JUAN, CHUECA, ANA, CABALLERO, JOSÉ LUIS, SAHRAWY, MARIAM
- Plant, cell and environment 2009 v.32 no.7 pp. 811-827
- Fragaria ananassa, autotrophs, carbon, chloroplasts, complementary DNA, embryophytes, evolution, hydrogen peroxide, isozymes, strawberries, yeasts
- A full-length FBPase cDNA has been isolated from Fragaria x ananassa (strawberry) corresponding to a novel putative chloroplastic FBPase but lacking the regulatory redox domain, a characteristic of the plastidial isoenzyme (cpFBPaseI). Another outstanding feature of this novel isoform, called cpFBPaseII, is the absence of the canonical active site. Enzymatic assays with cpFBPaseII evidenced clear Mg²⁺-dependent FBPase activity and a Km for fructose-1,6-bisphosphate (FBP) of 1.3 m m. Immunolocalization experiments and chloroplast isolation confirmed that the new isoenzyme is located in the stroma. Nevertheless, unlike cpFBPaseI, which is redox activated, cpFBPaseII did not increase its activity in the presence of either DTT or thioredoxin f (TRX f) and is resistant to H₂O₂ inactivation. Additionally, the novel isoform was able to complement the growth deficiency of the yeast FBP1 deletion fed with a non-fermentable carbon source. Furthermore, orthologues are restricted to land plants, suggesting that cpFBPaseII is a novel and an intriguing chloroplastic FBPase that emerged late in the evolution of photosynthetic organisms, possibly because of a pressing need of land plants.