Rana Satiander, Bhat Wajid Waheed, Dhar Niha, Pandith Shahzad A, Razdan Sumeer, Vishwakarma Ram, Lattoo Surrinder K
Plant Biotechnology Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu, Tawi-180001, India.
Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu, Tawi-180001, India.
BMC Biotechnol. 2014 Nov 23;14:89. doi: 10.1186/s12896-014-0089-5.
Pharmacological investigations position withanolides as important bioactive molecules demanding their enhanced production. Therefore, one of the pivotal aims has been to gain knowledge about complete biosynthesis of withanolides in terms of enzymatic and regulatory genes of the pathway. However, the pathway remains elusive at the molecular level. P450s monooxygenases play a crucial role in secondary metabolism and predominantly help in functionalizing molecule core structures including withanolides.
In an endeavor towards identification and characterization of different P450s, we here describe molecular cloning, characterization and expression analysis of two A-type P450s, WsCYP98A and WsCYP76A from Withania somnifera. Full length cDNAs of WsCYP98A and WsCYP76A have open reading frames of 1536 and 1545 bp encoding 511 (58.0 kDa) and 515 (58.7 kDa) amino acid residues, respectively. Entire coding sequences of WsCYP98A and WsCYP76A cDNAs were expressed in Escherichia coli BL21 (DE3) using pGEX4T-2 expression vector. Quantitative real-time PCR analysis indicated that both genes express widely in leaves, stalks, roots, flowers and berries with higher expression levels of WsCYP98A in stalks while WsCYP76A transcript levels were more obvious in roots. Further, transcript profiling after methyl jasmonate, salicylic acid, and gibberellic acid elicitations displayed differential transcriptional regulation of WsCYP98A and WsCYP76A. Copious transcript levels of both P450s correlated positively with the higher production of withanolides.
Two A-types P450 WsCYP98A and WsCYP76A were isolated, sequenced and heterologously expressed in E. coli. Both P450s are spatially regulated at transcript level showing differential tissue specificity. Exogenous elicitors acted as both positive and negative regulators of mRNA transcripts. Methyl jasmonate and salicylic acid resulted in copious expression of WsCYP98A and WsCYP76A. Enhanced mRNA levels also corroborated well with the increased accumulation of withanolides in response to elicitations. The empirical findings suggest that elicitors possibly incite defence or stress responses of the plant by triggering higher accumulation of withanolides.
药理学研究表明,睡茄内酯是重要的生物活性分子,需要提高其产量。因此,关键目标之一是了解睡茄内酯在该途径的酶基因和调控基因方面的完整生物合成。然而,该途径在分子水平上仍然难以捉摸。细胞色素P450单加氧酶在次生代谢中起关键作用,主要帮助包括睡茄内酯在内的分子核心结构功能化。
为了鉴定和表征不同的细胞色素P450,我们在此描述了来自印度人参的两种A型细胞色素P450,WsCYP98A和WsCYP76A的分子克隆、表征和表达分析。WsCYP98A和WsCYP76A的全长cDNA具有1536和1545 bp的开放阅读框,分别编码511(58.0 kDa)和515(58.7 kDa)个氨基酸残基。使用pGEX4T-2表达载体在大肠杆菌BL21(DE3)中表达WsCYP98A和WsCYP76A cDNA的完整编码序列。实时定量PCR分析表明,这两个基因在叶、茎、根、花和浆果中广泛表达,WsCYP98A在茎中的表达水平较高,而WsCYP76A转录本水平在根中更明显。此外,茉莉酸甲酯、水杨酸和赤霉素诱导后的转录谱显示了WsCYP98A和WsCYP76A的差异转录调控。两种细胞色素P450的大量转录水平与睡茄内酯的较高产量呈正相关。
分离出两种A型细胞色素P450 WsCYP98A和WsCYP76A,进行了测序并在大肠杆菌中进行了异源表达。两种细胞色素P450在转录水平上受到空间调控,表现出不同的组织特异性。外源诱导剂对mRNA转录本起正负调节作用。茉莉酸甲酯和水杨酸导致WsCYP98A和WsCYP76A大量表达。mRNA水平的提高也与诱导后睡茄内酯积累的增加密切相关。实验结果表明,诱导剂可能通过触发睡茄内酯的更高积累来激发植物的防御或应激反应。