Chemical screening of inhibitors specific for MdDOX-Co that cause an apple columnar tree-shape

ABSTRACT MdDOX-Co, the ectopic expression of which is considered to cause the apple columnar tree shape, belongs to the 2-oxoglutarate-dependent dioxygenase (2ODD) family. It adds a hydroxyl group to position 12 of gibberellins (GAs). However, the 2ODD enzymes related to GA biosynthesis and cataboli...

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Veröffentlicht in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2023-12, Vol.88 (1), p.63-69
Hauptverfasser: Okamoto, Keisuke, Inoue, Taiki, Nagano, Tsunesato, Miyazaki, Sho, Takahashi, Ikuo, Asami, Tadao, Okada, Kazunori, Okada, Kazuma, Nakajima, Masatoshi
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Sprache:eng
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Zusammenfassung:ABSTRACT MdDOX-Co, the ectopic expression of which is considered to cause the apple columnar tree shape, belongs to the 2-oxoglutarate-dependent dioxygenase (2ODD) family. It adds a hydroxyl group to position 12 of gibberellins (GAs). However, the 2ODD enzymes related to GA biosynthesis and catabolism are phylogenetically distinct from MdDOX-Co. Thus, it is possible that substrates other than GAs exist in MdDOX-Co. To identify the previously unidentified substrate(s) of MdDOX-Co, we searched for MdDOX-Co-specific inhibitors. Chemical screening using gas chromatography-mass spectrometry was performed to investigate the effects of 2400 compounds that inhibited the catalytic reaction of MdDOX-Co, but not the catabolic reaction of GA 2-oxidase, an enzyme involved in GA catabolism. By applying two positive compounds in Arabidopsis, a chemical 3-((2-chloro-6-fluorobenzyl)thio)-5,7-dimethyl-5H-pyrazolo[3,4-e][1,4,2]dithiazine-1,1-dioxide designated as TPDD that did not inhibit GA biosynthesis was selected. The structure-activity relationships among the TPDD analogs were also obtained. Graphical Abstract Graphical Abstract TPDD selectively inhibits the causative enzyme MdDOX-Co of columnarization without inhibiting the 2ODD enzymes required for gibberellin metabolism.
ISSN:1347-6947
1347-6947
DOI:10.1093/bbb/zbad142