WU Pei-zhen, DENG Lei, YUAN Yan-li, MA Zhou-jie, ZHANG Kai-wu, REN Hong, WANG Wei. Cloning and Bioinformatics Analysis of ZmASA2 Gene in Maize[J]. Seed, 2024, 43(6): 131-138. DOI: 10.16590/j.cnki.1001-4705.2024.06.131
Citation: WU Pei-zhen, DENG Lei, YUAN Yan-li, MA Zhou-jie, ZHANG Kai-wu, REN Hong, WANG Wei. Cloning and Bioinformatics Analysis of ZmASA2 Gene in Maize[J]. Seed, 2024, 43(6): 131-138. DOI: 10.16590/j.cnki.1001-4705.2024.06.131

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 encoding α subunit homologous gene of anthranilic acid synthase was cloned from corn B73 by RT-PCR technique, named ZmASA2. Amino acid sequence analysis showed that the total length of the cDNA fragment 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.
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