石榴PgUGT基因表达特性与重组表达分析
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1.南京林业大学林学院;2.日照市自然资源和规划局

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国家自然科学基金(31901341);江苏省自然科学基金(BK20180768);南京林业大学高层次人才科研启动基金(GXL2014070, GXL 2018032);江苏省高校优势学科建设工程(PAPD)


Expression Profiles and Recombinant Expression of PgUGT in Pomegranate
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    摘要:

    由糖基转移酶参与的糖基化反应是植物次生代谢产物合成中最广泛的一种修饰方式,也是次生代谢产物结构多样性的机制之一。本研究基于石榴(Punica granatum L.)转录组数据,以石榴果皮为材料,采用RT-PCR克隆得到了石榴UDP-糖基转移酶(UDP-glycosyltransferase, UGT)基因(PgUGT);采用生物信息学技术对编码蛋白的基本特性进行了分析,并构建了系统发育树;采用实时荧光定量PCR (qRT-PCR)分析了该基因在果实发育期内的表达模式;结合果实发育期内的总类黄酮和总花色苷含量,分析了基因表达与总类黄酮和总花色苷合成的关系;构建了PgUGT的原核表达载体,对其进行原核重组表达。结果表明:(1)PgUGT(GenBank登录号为MW414607)具有一个1557 bp的开放阅读框(ORF),编码518个氨基酸,预测蛋白分子质量为55.9 KD,等电点为6.55,为不稳定的亲水蛋白;PgUGT具有糖基转移酶家族保守的PSPG基序,属于GT-B糖基转移酶基因家族。进化树分析表明,该编码蛋白属于拟南芥UGT的F类群,与葡萄和草莓的UGT亲缘关系较近。(2)qRT-PCR结果表明,PgUGT的表达量在果实发育期内呈先升后降的模式,与总类黄酮含量的逐渐下降和总花色苷含量的逐渐上升趋势并不完全一致。(3)重组原核表达结果显示,重组质粒在大肠杆菌中为可溶性表达,表达的蛋白分子量约为58 KD。本结果为研究PgUGT在石榴类黄酮糖基化反应中的作用及功能奠定了基础。

    Abstract:

    The glycosylation reaction mediated by glycosyltransferases is not only a ubiquitous modification but also one of the structure diversity mechanisms for secondary metabolites synthesis. Based on the pomegranate transcriptomic data, a UDP-glycosyltransferase gene (PgUGT) was isolated from peels of ‘Taishanhong’ pomegranate by RT-PCR. Then the basic physicochemical properties and phylogenetic relationships were analyzed by bioinformatics method. The gene expression profiles during fruit developmental stages were obtained by quantitative real-time PCR (qRT-PCR). By combination with total flavonoid content and total anthocyanin content analysis, the relationships between gene transcription levels and total flavonoid content and total anthocyanin content were discussed. Subsequently, the PgUGT gene was constructed on the prokaryotic expression vector and recombinant expression were performed. The results were as follows: (1) The open reading frame (ORF) of PgUGT (GenBank No. MW414607) was 1557 bp, which encoded 518 amino acids. The molecular weight of protein was 55.9 kD, the isoelectric point was 6.55, the deduced protein was unstable hydrophilic one. PgUGT contained conserved PSPG motif, which belonged to GT-B glycosyltransferase superfamily. The phylogenetic trees analysis demonstrated that PgUGT was clustered into F group according to UGTs category of Arabidopsis thaliana, and was more closely related to that of grape and strawberry. (2) The qRT-PCR results demonstrated that the expression level of PgUGT exhibited a first-rise and then-fall pattern during fruit development, which was different from a gradual declining trend in total flavonoid content and gradual rising trend in total anthocyanin content. (3) The prokaryotic expression results showed that the recombinant plastid expressed in soluble form in E. coli expression systems. The size of fusion protein was approximately 58 KD as expected. The obtained results laid foundation for further revealing the roles and functions of PgUGT in flavonoid glycosylation reaction of pomegranate.

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  • 收稿日期:2021-11-09
  • 最后修改日期:2022-01-04
  • 录用日期:2022-01-04
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