首页|玉米ZmASA2基因的克隆与生物信息学分析

玉米ZmASA2基因的克隆与生物信息学分析

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邻氨基苯甲酸合成酶(Anthranilate synthase,AS),是存在于植物细胞中催化色氨酸合成的复合酶,由α亚基和β亚基组成.本研究采用RT-PCR技术,从玉米B73中克隆得到一个编码邻氨基苯甲酸合成酶α亚基同源基因的cDNA片段,命名为ZmASA2.氨基酸序列分析表明,该cDNA片段全长1 731 bp,预测编码一条含577个氨基酸的多肽,分子量为64.48 kD,理论等电点为6.64.生物信息学分析表明,ZmASA2属于定位在细胞质中的亲水性蛋白,二级结构主要为α螺旋.系统发育分析表明,ZmASA2蛋白与南荻和高粱的AS在进化上种属关系最近.qRT-PCR结果显示,ZmASA2在授粉后30 d籽粒表达量最高,其次是茎.
Cloning and Bioinformatics Analysis of ZmASA2 Gene in Maize
Anthranilate synthase(AS)is a complex enzyme that catalyzes the synthesis of tryptophan in plant cells,consisting of α subunits and β subunits.In this study,a cDNA fragment encodingα subunit homologous gene of anthranilic acid synthase was cloned from corn B73 by RT-PCR tech-nique,named ZmASA2.Amino acid sequence analysis showed that the total length of the cDNA frag-ment was 1 731 bp,and it was predicted to code a polypeptide containing 577 amino acids,with a molecular weight of about 64.48 kD and a theoretical isoelectric point of 6.64.Bioinformatics analysis showed that ZmASA2 was a hydrophilic protein located in the cytoplasm,and its secondary structure was mainly α helix.Phylogenetic analysis showed that ZmASA2 protein was the closest phylogenetic relation to AS of Miscanthus lutarioriparius and sorghum.The results of qRT-PCR showed that the expression of ZmASA2 was the highest at 30 days after pollination,followed by the stem.

maizeanthranilate synthasebioinformatics analysisexpression analysis

吴培珍、邓磊、袁艳丽、马周杰、张开武、任洪、王伟

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贵州大学生命科学学院/农业生物工程研究院,山地植物资源保护与种质创新教育部重点实验室,贵阳 550025

贵州省农业科学院旱粮研究所,贵阳 550006

农业农村部喀斯特山区玉米生物学与遗传育种重点实验室,贵阳 550006

玉米 邻氨基苯甲酸合成酶 生物信息学分析 表达分析

国家自然科学基金国家玉米产业技术体系贵州省科技计划项目贵州省科技计划项目

32060461CARS-02-91黔科中引地[2022]4011黔科合服企[2022]007

2024

种子
贵州省种子管理站 贵州省种子学会 中国种子协会

种子

CSTPCD北大核心
影响因子:0.502
ISSN:1001-4705
年,卷(期):2024.43(6)