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鸟氨酸脱羧酶的代谢特征

Metabolic Characterization of Ornithine Decarboxylase.

作者信息

Zhao Tengfei, Wang Changjian, Bai Feng, Li Siqi, Yang Chunxian, Zhang Fangyuan, Bai Ge, Chen Min, Lan Xiaozhong, Liao Zhihua

机构信息

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.

Tobacco Breeding and Biotechnology Research Center, Yunnan Academy of Tobacco Agricultural Sciences, Key Laboratory of Tobacco Biotechnological Breeding, National Tobacco Genetic Engineering Research Center, Kunming, China.

出版信息

Front Plant Sci. 2019 Feb 27;10:229. doi: 10.3389/fpls.2019.00229. eCollection 2019.

Abstract

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.

摘要

鸟氨酸脱羧酶(ODC)催化鸟氨酸脱羧生成腐胺,腐胺是多胺和托烷生物碱(TAs)的关键前体。在此,为了深入研究ODC在多胺/TAs生物合成中的作用,并为工程化生产多胺/TAs提供一个候选基因,从一种产TA的植物中对ODC基因()进行了表征。我们的系统发育分析表明,HnODC与植物的ODC酶聚类在一起。实验工作表明,在根中高表达,并受茉莉酸甲酯(MeJA)诱导。在MeJA处理中,根中腐胺和N-甲基腐胺的产量均显著提高,而叶中腐胺、亚精胺和精胺的含量均显著增加。相比之下,MeJA对该植物中莨菪碱或东莨菪碱的产量没有显著影响。基于这些结果,纯化了50 kDa带His标签的HnODC蛋白用于酶活性测定。当向HnODC中加入鸟氨酸时,通过高效液相色谱法检测到了腐胺产物,表明HnODC催化鸟氨酸形成腐胺。最后,我们还研究了HnODC的酶动力学特性。在pH 8.0和30°C条件下,其对鸟氨酸的Km、Vmax和kcat值分别为2.62±0.11 mM、1.87±0.023 nmol min-1 μg-1和1.57±0.利用这些结果,纯化了50 kDa带His标签的HnODC蛋白用于酶活性测定。当向HnODC中加入鸟氨酸时,通过高效液相色谱法检测到了腐胺产物,表明HnODC催化鸟氨酸形成腐胺。最后,我们还研究了HnODC的酶动力学特性。在pH 8.0和30°C条件下,其对鸟氨酸的Km、Vmax和kcat值分别为2.62±0.11 mM、1.87±0.023 nmol min-1 μg-1和1.57±0.015 s-1。HnODC酶显示出比大多数已报道的植物ODC更高的催化效率,这表明它可能是工程化多胺/TAs生物合成的理想候选基因。 015 s-1。HnODC酶显示出比大多数已报道的植物ODC更高的催化效率,这表明它可能是工程化多胺/TAs生物合成的理想候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec5/6400997/702ef10fd280/fpls-10-00229-g001.jpg

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