On the substrate- and stereospecificity of the plant carotenoid cleavage dioxygenase 7
KAUST DepartmentBiological and Environmental Science and Engineering (BESE) Division
Center for Desert Agriculture
Plant Science Program
Online Publication Date2014-03-28
Print Publication Date2014-05-02
Permanent link to this recordhttp://hdl.handle.net/10754/563521
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AbstractStrigolactones are phytohormones synthesized from carotenoids via a stereospecific pathway involving the carotenoid cleavage dioxygenases 7 (CCD7) and 8. CCD7 cleaves 9-cis-β-carotene to form a supposedly 9-cis-configured β-apo-10′-carotenal. CCD8 converts this intermediate through a combination of yet undetermined reactions into the strigolactone-like compound carlactone. Here, we investigated the substrate and stereo-specificity of the Arabidopsis and pea CCD7 and determined the stereo-configuration of the β-apo-10′-carotenal intermediate by using Nuclear Magnetic Resonance Spectroscopy. Our data unequivocally demonstrate the 9-cis-configuration of the intermediate. Both CCD7s cleave different 9-cis-carotenoids, yielding hydroxylated 9-cis-apo-10′-carotenals that may lead to hydroxylated carlactones, but show highest affinity for 9-cis-β-carotene. © 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
CitationBruno, M., Hofmann, M., Vermathen, M., Alder, A., Beyer, P., & Al-Babili, S. (2014). On the substrate- and stereospecificity of the plant carotenoid cleavage dioxygenase 7. FEBS Letters, 588(9), 1802–1807. doi:10.1016/j.febslet.2014.03.041
SponsorsThis work was supported by the German Research Foundation (DFG) Grant AL 892/1-4 and by the EU (METAPRO; FP7 KBBE-2009-3-1-01).
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