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Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase
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 O...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400997/ https://www.ncbi.nlm.nih.gov/pubmed/30873201 http://dx.doi.org/10.3389/fpls.2019.00229 |
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author | Zhao, Tengfei Wang, Changjian Bai, Feng Li, Siqi Yang, Chunxian Zhang, Fangyuan Bai, Ge Chen, Min Lan, Xiaozhong Liao, Zhihua |
author_facet | Zhao, Tengfei Wang, Changjian Bai, Feng Li, Siqi Yang, Chunxian Zhang, Fangyuan Bai, Ge Chen, Min Lan, Xiaozhong Liao, Zhihua |
author_sort | Zhao, Tengfei |
collection | PubMed |
description | 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 (HnODC) was characterized from Hyoscyamus niger, a TA-producing plant. Our phylogenetic analysis revealed that HnODC was clustered with ODC enzymes of plants. Experimental work showed HnODC highly expressed in H. niger roots and induced by methyl jasmonate (MeJA). In the MeJA treatment, the production of both putrescine and N-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 H. niger 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 K(m), V(max), and K(cat) values for ornithine were respectively 2.62 ± 0.11 mM, 1.87 ± 0.023 nmol min(-1) μg(-1) and 1.57 ± 0.015 s(-1), 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. |
format | Online Article Text |
id | pubmed-6400997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64009972019-03-14 Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase Zhao, Tengfei Wang, Changjian Bai, Feng Li, Siqi Yang, Chunxian Zhang, Fangyuan Bai, Ge Chen, Min Lan, Xiaozhong Liao, Zhihua Front Plant Sci Plant Science 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 (HnODC) was characterized from Hyoscyamus niger, a TA-producing plant. Our phylogenetic analysis revealed that HnODC was clustered with ODC enzymes of plants. Experimental work showed HnODC highly expressed in H. niger roots and induced by methyl jasmonate (MeJA). In the MeJA treatment, the production of both putrescine and N-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 H. niger 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 K(m), V(max), and K(cat) values for ornithine were respectively 2.62 ± 0.11 mM, 1.87 ± 0.023 nmol min(-1) μg(-1) and 1.57 ± 0.015 s(-1), 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. Frontiers Media S.A. 2019-02-27 /pmc/articles/PMC6400997/ /pubmed/30873201 http://dx.doi.org/10.3389/fpls.2019.00229 Text en Copyright © 2019 Zhao, Wang, Bai, Li, Yang, Zhang, Bai, Chen, Lan and Liao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Zhao, Tengfei Wang, Changjian Bai, Feng Li, Siqi Yang, Chunxian Zhang, Fangyuan Bai, Ge Chen, Min Lan, Xiaozhong Liao, Zhihua Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title | Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title_full | Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title_fullStr | Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title_full_unstemmed | Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title_short | Metabolic Characterization of Hyoscyamus niger Ornithine Decarboxylase |
title_sort | metabolic characterization of hyoscyamus niger ornithine decarboxylase |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400997/ https://www.ncbi.nlm.nih.gov/pubmed/30873201 http://dx.doi.org/10.3389/fpls.2019.00229 |
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