Abamine as a basis for new designs of regulators of strigolactone production
Nobutaka KitahataShinsaku ItoAtsutaka KatoKotomi UenoTakeshi NakanoKaori YoneyamaKoichi YoneyamaTadao Asami
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Abstract:
Nine-cis-epoxycarotenoid dioxygenase (NCED), belonging to the family of carotenoid-cleaving dioxygenases (CCDs), is the rate-limiting step in the abscisic acid (ABA) biosynthetic pathway in plants. Abamine is the first reported abscisic acid biosynthesis inhibitor to target NCED. Its utility has also been considered in the inhibition of other enzymes. As CCDs other than NCED are also involved in the strigolactone biosynthetic pathway, abamine may affect strigolactone biosynthesis. In this study, we found that abamine decreases the level of strigolactones in several plant species and reduces the germination rate of Orobanche minor seeds co-grown with tobacco. Taken together, these data suggest that abamine may be used as a scaffold for the development of specific regulators of strigolactone production.Keywords:
Strigolactone
Orobanche
In contrast to animals,plants and microorganisms depend on the endogenous riboflavin by biologically synthesis. Therefore,the inhibitors against key enzymes in the riboflavin biosynthesis pathway can be devel-oped into fungicides or herbicides which have non-toxic effects on people and livestock. Advances of the studies on the screening models for inhibitors against riboflavin biosynthesis are reviewed and the possible hot pot in the future studies on the bio-control agents are also discussed. Three enzymes,DHBP synthase,lumazine synthase(LS) and riboflavin synthase(RS) are respectively responsible for the last three kind of biological reactions during the riboflavin biosynthesis. With three enzymes DHBPS,LS and RS as targets,the compounds against the riboflavin synthesis in vitro and in vivo could be efficiently screened out. New screening targets and models contribute to the development of new bio-control agents.
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Coenzyme A
Metabolic pathway
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Strigolactones are highly potent germination stimulants for seeds of the parasitic weeds Striga and Orobanche spp. 4-Hydroxy-GR24 and 4-acetoxy-GR24 were prepared and their abilities to induce seed germination of Striga gesnerioides evaluated. Optically active (8bR,2'R)-isomers induced germination, although the racemic diastereomers were inactive. In contrast, the stereoisomer of GR24 with the same configuration induced negligible germination. Some stereoisomers of GR24 and its analogues acted as effective antagonists for induction of seed germination by cowpea root exudates. These results suggest that both an oxygenated substituent at C-4 and the configuration of the tricyclic lactone and the D-ring are essential structural requirements for induction of germination in S. gesnerioides seeds.
Orobanche
Strigolactone
Asymmetric induction
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o-Succinylbenzoate: coenzyme A ligase, an enzyme involved in menaquinone biosynthesis, was purified from Mycobacterium phlei and characterized with respect to isoelectric point, molecular weight, pH optimum, temperature optimum and kinetic data. The enzyme hydrolyses ATP to AMP. The substrate and cofactor specificity of the enzyme was tested with analogues of o-succinylbenzoic acid, different nucleotides, thiols and divalent cations. The enzyme appears to possess broad specificity for substrates and cofactors.
Coenzyme A
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The ntd operon in Bacillus subtilis is essential for biosynthesis of 3,3′-neotrehalosadiamine (NTD), an unusual nonreducing disaccharide reported to have antibiotic properties. It has been proposed that the three enzymes encoded within this operon, NtdA, NtdB, and NtdC, constitute a complete set of enzymes required for NTD synthesis, although their functions have never been demonstrated in vitro. We now report that these enzymes catalyze the biosynthesis of kanosamine from glucose-6-phosphate: NtdC is a glucose-6-phosphate 3-dehydrogenase, NtdA is a pyridoxal phosphate-dependent 3-oxo-glucose-6-phosphate:glutamate aminotransferase, and NtdB is a kanosamine-6-phosphate phosphatase. None of these enzymatic reactions have been reported before. This pathway represents an alternate route to the previously reported pathway from Amycolatopsis mediterranei which derives kanosamine from UDP-glucose.
Pyridoxal phosphate
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Strigolactones (SLs), phytohormones that inhibit shoot branching in plants, promote the germination of root-parasitic plants, such as Striga spp. and Orobanche spp., which drastically reduces the crop yield. Therefore, reducing SL production via chemical treatment may increase the crop yield. To design specific inhibitors, it is valid to utilize the substrate structure of the target proteins as lead compounds. In this study, we focused on Os900, a rice enzyme that oxidizes the SL precursor carlactone (CL) to 4-deoxyorobanchol (4DO), and synthesized 10 CL derivatives. The effects of the synthesized CL derivatives on SL biosynthesis were evaluated by the Os900 enzyme assay in vitro and by measuring 4DO levels in rice root exudates. We identified some CL derivatives that inhibited SL biosynthesis in vitro and in vivo.
Strigolactone
Orobanche
Striga hermonthica
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Nine-cis-epoxycarotenoid dioxygenase (NCED), belonging to the family of carotenoid-cleaving dioxygenases (CCDs), is the rate-limiting step in the abscisic acid (ABA) biosynthetic pathway in plants. Abamine is the first reported abscisic acid biosynthesis inhibitor to target NCED. Its utility has also been considered in the inhibition of other enzymes. As CCDs other than NCED are also involved in the strigolactone biosynthetic pathway, abamine may affect strigolactone biosynthesis. In this study, we found that abamine decreases the level of strigolactones in several plant species and reduces the germination rate of Orobanche minor seeds co-grown with tobacco. Taken together, these data suggest that abamine may be used as a scaffold for the development of specific regulators of strigolactone production.
Strigolactone
Orobanche
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Identification
Moiety
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Strigolactones (SLs) are carotenoid-derived plant hormones involved in the development of various plants. SLs also stimulate seed germination of the root parasitic plants, Striga spp. and Orobanche spp., which reduce crop yield. Therefore, regulating SL biosynthesis may lessen the damage of root parasitic plants. Biosynthetic inhibitors effectively control biological processes by targeted regulation of biologically active compounds. In addition, biosynthetic inhibitors regulate endogenous levels in developmental stage- and tissue-specific manners. To date, although some chemicals have been found as SL biosynthesis inhibitor, these are derived from only three lead chemicals. In this study, to find a novel lead chemical for SL biosynthesis inhibitor, 27 nitrogen-containing heterocyclic derivatives were screened for inhibition of SL biosynthesis. Triflumizole most effectively reduced the levels of rice SL, 4-deoxyorobanchol (4DO), in root exudates. In addition, triflumizole inhibited endogenous 4DO biosynthesis in rice roots by inhibiting the enzymatic activity of Os900, a rice enzyme that converts the SL intermediate carlactone to 4DO. A Striga germination assay revealed that triflumizole-treated rice displayed a reduced level of germination stimulation for Striga. These results identify triflumizole as a novel lead compound for inhibition of SL biosynthesis.
Strigolactone
Orobanche
Striga hermonthica
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