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Two CYP716A subfamily cytochrome P450 monooxygenases of sweet basil play similar but nonredundant roles in ursane‐ and oleanane‐type pentacyclic triterpene biosynthesis

机译：两种CYP716A亚家族细胞色素P450甜罗勒的单氧基酶在熊烷和烯酮型五环三萜生物合成中起相似但非恒生的作用

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Rajesh Chandra Misra; Shubha Sharma; Anchal Garg; Chandan Singh Chanotiya; Sumit Ghosh;
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1. Methyl Jasmonate-Elicited Transcriptional Responses and Pentacyclic Triterpene Biosynthesis in Sweet Basil1[C][W] [J] . Rajesh Chandra Misra, Protiti Maiti, Chandan Singh Chanotiya, Plant physiology . 2014,第2期

机译：茉莉酸甲酯引起的转录反应和甜蓬蒿中五环三萜的生物合成[C] [W]
2. Pentacyclic triterpenes of the lupane, oleanane and ursane group as tools in cancer therapy [J] . LaszczykM.N. Planta medica: Natural products and medicinal plant research . 2009,第15期

机译：紫杉烷，齐墩果烷和戊烷的五环三萜类化合物在癌症治疗中的作用
3. Cytochrome P450 CYP716A254 catalyzes the formation of oleanolic acid from β-amyrin during oleanane-type triterpenoid saponins biosynthesis in Anemone flaccida [J] . Chuansong Zhan, Shakeel Ahmed, Sheng Hu, Biochemical and Biophysical Research Communications . 2018,第1期

机译：细胞色素P450 CYP716A254催化在海葵Flaccida的烯烷型三萜类皂苷生物合成中从β-氨纶中形成OleAlic酸的形成
4. The role of the nuclear receptors CAR and PXR in the drug induced transcriptional regulation of the murine CYP2C subfamily of cytochromes P450 monooxygenases. [D] . Jackson, Jonathan Patrick. 2006

机译：核受体CAR和PXR在药物中诱导细胞色素P450单加氧酶的鼠CYP2C亚家族的转录调控。
5. Methyl Jasmonate-Elicited Transcriptional Responses and Pentacyclic Triterpene Biosynthesis in Sweet Basil [O] . Rajesh Chandra Misra, Protiti Maiti, Chandan Singh Chanotiya, 2014

机译：甜罗勒茉莉酸甲酯引起的转录反应和五环三萜的生物合成
6. Production of 3-acetylnivalenol by transgenic Fusarium graminearum expressing Tri13 of type A trichothecene-producer: participation of the encoded cytochrome P450 monooxygenase in type B trichothecene biosynthesis [O] . Kazuyuki MAEDA, Takeshi TOKAI, Hinayo ICHIKAWA, 2012

机译：通过转基因镰刀蛋白的制备3-乙酰基苯酚，表达Trichothecene-Metucer的Tri13：编码细胞色素P450单氧基酶在B型Trichothecene生物合成中的参与

Two CYP716A subfamily cytochrome P450 monooxygenases of sweet basil play similar but nonredundant roles in ursane‐ and oleanane‐type pentacyclic triterpene biosynthesis

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