通过转录组学方法鉴定苯丙氨酸氨裂解酶并揭示 Gymnema sylvestre R. Br 中黄酮类化合物的生物合成过程

IF 3.5 Q3 Biochemistry, Genetics and Molecular Biology Journal of Genetic Engineering and Biotechnology Pub Date : 2024-02-13 DOI:10.1016/j.jgeb.2023.100344
Kuldeepsingh A. Kalariya, Ravina R. Mevada, Manish Das
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引用次数: 0

摘要

背景Gymnema sylvestre R.Br.是糖尿病患者中著名的药用植物,因其含有石膏酸。它还含有黄酮类化合物,而黄酮类化合物是其他各种产品的重要成分。虽然目前已有一些关于石膏酸、聚氧孕烷、微 RNA 和光合效率生物合成的分子信息,但还没有关于该植物中黄酮类化合物生物合成的基因水平信息。从冬季采集的裸冠菊叶片中提取 RNA,制备 cDNA 文库并用于新一代测序。准备了新的转录组,并从转录组数据中确定了参与类黄酮生物合成的 13 个主要基因的编码 DNA 序列(CDS)。含有全长 CDS 的苯丙氨酸氨裂解酶基因被用于硅学蛋白质建模和随后的质量评估。然后将这些模型与公开数据库进行比较。为了确认这些基因的身份,使用 NCBI BLAST 工具进行了相似性搜索。结果因此,在本研究中,我们通过研究鹅掌楸中表达的转录本,努力从分子角度揭示黄酮类化合物的生物合成途径。共有十三个主要基因的基因序列,即苯丙氨酸氨裂解酶、4-香豆酸 CoA 连接酶、肉桂酸 4-羟化酶、莽草酸 O-羟基肉桂酰转移酶、香豆酰醌(香豆酰莽草酸)3′-单加氧酶、咖啡酰-CoA O-甲基转移酶、查尔酮合成酶、查尔酮异构酶、柚皮苷 3-二加氧酶、根据转录组数据,确定了黄烷醇合成酶、黄酮 3′-单氧化酶、黄烷酮 7-O-Glucoside 2″-O-beta-L-rhyamnosyltransferase 和白花青素二氧化酶,并说明了黄酮类化合物生物合成的推定途径。结论这项转录组研究有助于在基因水平上深入了解黄酮类化合物在整个植物中的生物合成过程,是对非模式植物裸冠菊(Gymnema sylvestre perticullarly)的首次报道。
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Characterization of phenylalanine ammonia lyase and revealing flavonoid biosynthesis in Gymnema sylvestre R. Br through transcriptomic approach

Background

Gymnema sylvestre R.Br. is famous medicinal plant among diabetics for its gymnemic acid content. It also contains flavonoids, which are an essential component in various other products. Though some molecular information on the biosynthesis of gymnemic acid, polyoxypregnane, micro RNAs and photosynthetic efficiency is available, there is no gene level information available on the biosynthesis of flavonoids in this plant. RNA was extracted from winter-collected Gymnema sylvestre leaves and cDNA libraries were prepared and used for next generation sequencing. De novo transcriptome assembly were prepared and Coding DNA Sequences (CDS) of 13 major genes involved in flavonoids biosynthesis were identified from transcriptome data. Phenylalanine ammonia lyase gene containing full-length CDS was employed for in silico protein modelling and subsequent quality assessment. These models were then compared against publicly available databases. To confirm the identification of these genes, a similarity search was conducted using the NCBI BLAST tool.

Results

Therefore, in the present study, an effort has been made to provide molecular insights into flavonoid biosynthesis pathway by examining the expressed transcripts in G.sylvestre. Gene sequences of total thirteen major genes viz., phenylalanine ammonia lyase, 4-coumarate CoA ligase, cinnamic acid 4-hydroxylase, shikimate O-hydroxycinnamoyl transferase, coumaroyl quinate (coumaroyl shikimate) 3′-monooxygenase, caffeoyl-CoA O-methyltransferase, chalcone synthase, chalcone isomerase, naringenin 3-dioxygenase, flavanol synthase, flavonoid 3′-monooxygenase, Flavanone 7-O-glucoside 2″-O-beta-L-rhyamnosyltransferase and leucoanthocyanidin dioxygenase were identified and a putative pathway of flavonoids biosynthesis has been illustrated based on transcriptome data.

Conclusions

This transcriptome study has contributed gene-level insights into the biosynthesis of flavonoids in plants as a whole and represents the first report within a non-model plant, Gymnema sylvestre perticullarly.

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来源期刊
Journal of Genetic Engineering and Biotechnology
Journal of Genetic Engineering and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
5.70
自引率
5.70%
发文量
159
审稿时长
16 weeks
期刊介绍: Journal of genetic engineering and biotechnology is devoted to rapid publication of full-length research papers that leads to significant contribution in advancing knowledge in genetic engineering and biotechnology and provide novel perspectives in this research area. JGEB includes all major themes related to genetic engineering and recombinant DNA. The area of interest of JGEB includes but not restricted to: •Plant genetics •Animal genetics •Bacterial enzymes •Agricultural Biotechnology, •Biochemistry, •Biophysics, •Bioinformatics, •Environmental Biotechnology, •Industrial Biotechnology, •Microbial biotechnology, •Medical Biotechnology, •Bioenergy, Biosafety, •Biosecurity, •Bioethics, •GMOS, •Genomic, •Proteomic JGEB accepts
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