Molecular characterization and phylogenetic analysis of kaurene synthase protein in Stevia rebaudiana MS007

Nur Fathiah Rosilan, M. Samsulrizal, Norsyahida Rani, N. Samsulrizal, Z. Zainuddin, T. Sundram
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Abstract

Stevia rebaudiana is a plant under the Asteraceae family and has been reported as a healthier alternative to sugar. Steviol glycosides (SGs) is the group of secondary metabolites responsible for the sweet taste. Among nine SGs synthesised by S. rebaudiana, stevioside and rebaudioside A are the sweetest. The biosynthetic pathway of SGs partly involves conversion of geranylgeranyl diphosphate (GGDP) into steviol, catalysed by ent- kaurene synthase (KS), ent-copalyl diphosphate synthase (CPPS), and kaurene oxidase (KO). This study focuses on in silico molecular characterization and phylogenetic analysis of KS from Malaysia’s S. rebaudiana MS007 variety (Stevia MS007). The transcriptomic dataset of S. rebaudiana accession MS007 was used in initial experiment toward analysing the KS. Through the blastx homology search using transcriptomic dataset query Cluster-31069.42907, the Stevia rebaudiana kaurene synthase (SrKS) sequence was identified with the highest similarity percentage identity (99.62%). The protein domain prediction using InterPro yields IPR005630 (terpene synthase metal-binding domain) at positions 490 to 755 and IPR001906 (terpene synthase-N-terminal-domain) at positions 258 to 477. Multiple sequence alignment was conducted using MUSCLE and MEGA-X as phylogenetic tree analysis tool for constructing the phylogenetic analysis tree. Based on the bootstrap value from the phylogenetic analysis, Cluster-31069.42907 represents relationships between the ancestors. Since both Helianthus annuus and S. rebaudiana are Asteraceae species, the bootstrap value for both species was 100%. In conclusion, this research contributes to a better understanding of Stevia MS007 KS via in silico analysis.
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甜菊MS007中丁香烯合成酶蛋白的分子特征及系统发育分析
甜菊糖是一种菊科植物,据报道是一种更健康的糖替代品。甜菊醇糖苷(SGs)是一组负责甜味的次级代谢物。其中甜菊糖苷和甜菊糖苷A最甜。SGs的生物合成途径部分涉及在丁香烯合成酶(KS)、丁香烯共酯二磷酸合成酶(CPPS)和丁香烯氧化酶(KO)的催化下,将香叶基二磷酸(GGDP)转化为甜菊醇。本文对马来西亚甜菊菊MS007品种(S. rebaudiana MS007)的KS进行了硅分子表征和系统发育分析。本研究利用白藜芦醇(S. reaudiana)稻种MS007的转录组学数据进行初步研究。通过转录组数据查询Cluster-31069.42907的blastx同源性搜索,鉴定出甜叶菊(Stevia rebaudiana kaurene synthase, SrKS)序列的相似性百分比最高(99.62%)。使用InterPro进行蛋白结构域预测,得到位于490 ~ 755位的IPR005630(萜烯合成酶金属结合结构域)和位于258 ~ 477位的IPR001906(萜烯合成酶- n端结构域)。利用MUSCLE和MEGA-X作为系统发育树分析工具进行多序列比对,构建系统发育分析树。基于系统发育分析的bootstrap值,Cluster-31069.42907表示祖先之间的关系。由于一年生向日葵(Helianthus annuus)和白玉兰(S. reaudiana)均为菊科植物,因此两种植物的自举值均为100%。总之,本研究有助于通过芯片分析更好地了解甜菊糖MS007 KS。
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来源期刊
Asia-pacific Journal of Molecular Biology and Biotechnology
Asia-pacific Journal of Molecular Biology and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
0.90
自引率
0.00%
发文量
25
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