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勃氏甜龙竹DbFRK2和DbHXK5基因的克隆、表达与功能初探

王勇梅 姜博楠 张士奇 王浩 马永朝 王曙光 李娟

核农学报2026,Vol.40Issue(8):1540-1551,12.
核农学报2026,Vol.40Issue(8):1540-1551,12.DOI:10.11869/j.issn.1000-8551.2026.08.1540

勃氏甜龙竹DbFRK2和DbHXK5基因的克隆、表达与功能初探

Cloning,Expression,and Preliminary Functional Analysis of DbFRK2 and DbHXK5 Genes in Dendrocalamus brandisii(Munro)Kurz.

王勇梅 1姜博楠 1张士奇 1王浩 1马永朝 1王曙光 2李娟3

作者信息

  • 1. 西南林业大学生物与食品工程学院,云南 昆明 650224
  • 2. 西南林业大学生物与食品工程学院,云南 昆明 650224||西南林业大学云南省丛生竹重点实验室,云南 昆明 650224||西南林业大学竹藤科学研究院,云南 昆明 650224
  • 3. 西南林业大学生物与食品工程学院,云南 昆明 650224||西南林业大学云南省丛生竹重点实验室,云南 昆明 650224
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摘要

Abstract

Fructokinase and hexokinase are key plant enzymes that catalyze fructose phosphorylation and playing central roles in glycolysis,and carbohydrate metabolism.To explore the potential functions of DbFRK2 and DbHXK5 in sweetness formation of Dendrocalamus brandisii bamboo shoots,this study cloned DbFRK2 and DbHXK5 using reverse transcription-polymerase chain reaction(RT-PCR).Gene expression patterns were analyzed using quantitative real-time polymerase chain reaction(qRT-PCR),and fructose content and related metabolic enzyme activities were measured across various developmental stages of bamboo shoots.The results revealed that the open reading frame of DbFRK2 is 993 bp in length,encoding a protein of 331 amino acids.This protein contains conserved domains characteristic of the pfkB carbohydrate phosphofructokinase family,including three substrate-binding regions,six ATP-binding sites,and the PLN02323 conserved domain.Phylogenetic analysis indicated that DbFRK2 shares a close relationship with the fructokinase gene in Lolium rigidum.DbHXK5 possesses an open reading frame of 1 422 bp,encoding a protein of 474 amino acids.This protein contains the complete ASKHA_NBD_HK_plant domain,confirming its classification within the plant hexokinase family.It shows the mostly close relationship to Phyllostachys edulis in phylogenetic analysis.qRT-PCR results demonstrated that both DbFRK2 and DbHXK5 expression levels,as well as FRK and HXK enzyme activities,increased progressively during bamboo shoot development.While fructose content gradually decreased.These findings suggest that DbFRK2 and DbHXK5 may be involved in regulating fructose metabolism in bamboo shoots.This study provides a foundation for further elucidating the functions of DbFRK2 and DbHXK5 in sugar metabolism in Dendrocalamus brandisii,thereby offering theoretical support for the improvement of bamboo shoot quality and guidance for production practices.

关键词

勃氏甜龙竹/果糖激酶/己糖激酶/基因克隆/表达分析

Key words

Dendrocalamus brandisii/fructokinase/hexokinase/gene clone/expression analysis

分类

农业科技

引用本文复制引用

王勇梅,姜博楠,张士奇,王浩,马永朝,王曙光,李娟..勃氏甜龙竹DbFRK2和DbHXK5基因的克隆、表达与功能初探[J].核农学报,2026,40(8):1540-1551,12.

基金项目

国家自然科学基金青年科学基金项目(31800506),"十四五"国家重点研发计划项目(2021YFD2200503-4) (31800506)

核农学报

1000-8551

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