Metabolic Characterization of Ornithine Decarboxylase.

Front Plant Sci

Key Laboratory of Eco-Environments in Three Gorges Reservoir Region (Ministry of Education), Chongqing Engineering Research Centre for Sweet Potato, TAAHC-SWU Medicinal Plant Joint R&D Centre, School of Life Sciences, Southwest University, Chongqing, China.

Published: February 2019

Ornithine decarboxylase (ODC) catalyzes ornithine decarboxylation to yield putrescine, a key precursor of polyamines, and tropane alkaloids (TAs). Here, to investigate in depth the role of ODC in polyamine/TA biosynthesis and to provide a candidate gene for engineering polyamine/TA production, the ODC gene () was characterized from , a TA-producing plant. Our phylogenetic analysis revealed that HnODC was clustered with ODC enzymes of plants. Experimental work showed highly expressed in roots and induced by methyl jasmonate (MeJA). In the MeJA treatment, the production of both putrescine and -methylputrescine were markedly promoted in roots, while contents of putrescine, spermidine, and spermine were all significantly increased in leaves. By contrast, MeJA did not significantly change the production of either hyoscyamine or scopolamine in plants. Building on these results, the 50-kDa His-tagged HnODC proteins were purified for enzymatic assays. When ornithine was fed to HnODC, the putrescine product was detected by HPLC, indicating HnODC catalyzed ornithine to form putrescine. Finally, we also investigated the enzymatic kinetics of HnODC. Its , , and values for ornithine were respectively 2.62 ± 0.11 mM, 1.87 ± 0.023 nmol min μg and 1.57 ± 0.015 s, at pH 8.0 and at 30°C. The HnODC enzyme displays a much higher catalytic efficiency than most reported plant ODCs, suggesting it may be an ideal candidate gene for engineering polyamine/TA biosynthesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400997PMC
http://dx.doi.org/10.3389/fpls.2019.00229DOI Listing

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