生物学杂志 ›› 2026, Vol. 43 ›› Issue (5): 34-.doi: 10.3969/j.issn.2095-1736.2026.05.034

• 研究报告 • 上一篇    下一篇

cit1基因对黄曲霉生长发育和毒素合成的影响

谢春兰1,2, 杨坤龙2,3, 秦 贝1,2, 谢 瑞1,2   

  1. 1. 山东协和学院 医学院, 济南 250109; 2. 福建省病原真菌与真菌毒素重点实验室, 福州 350002;
    3. 江苏师范大学 生命科学学院, 徐州 221116
  • 出版日期:2026-10-18 发布日期:2026-10-20
  • 通讯作者: 谢瑞,博士,副教授,研究方向为生物化学与分子生物学,E-mail:xr37154@163.com
  • 作者简介:谢春兰,硕士,研究方向为生物化学与分子生物学,E-mail:2833102314@qq.com
  • 基金资助:
    山东省自然科学基金项目(ZR2025QC212); 山东协和学院高层次人才科研启动经费项目(SDXHQD2024031)

Effect of the cit1 gene on Aspergillus flavus development and aflatoxin biosynthesis

XIE Chunlan1,2, YANG Kunlong2,3, QIN Bei1,2, XIE Rui1,2   

  1. 1. School of Medicine, Shandong Xiehe University, Jinan 250109, China; 2. Key Laboratory of Pathogenic
    Fungi and Mycotoxins of Fujian Province, Fuzhou 350002, China; 3. School of Life Sciences, Jiangsu Normal
    University, Xuzhou 221116, China
  • Online:2026-10-18 Published:2026-10-20

摘要: 黄曲霉产生的次级代谢产物黄曲霉毒素AFB1具有强致癌性,对人体健康和农业经济造成严重危害。黄曲霉中cit1基因编码柠檬酸合酶(CIT),该酶催化乙酰辅酶A和草酰乙酸生成柠檬酸从而开始三羧酸(TCA)循环,参与真核生物生长发育、细胞凋亡和癌细胞增殖过程的调控。了解Cit1蛋白在黄曲霉中的调控机制,为黄曲霉的生物防控提供新视角。本研究通过生物信息学手段分析,确定Cit1蛋白在曲霉属物种间高度保守。通过同源重组手段构建cit1基因缺失菌株,经表型实验、qRT-PCR实验初步探究cit1基因缺失对黄曲霉生长发育及致病性的影响。结果显示,Δcit1菌株的菌落直径显著减小且孢子数量和孢子梗形态相较野生型出现明显差异,该缺陷菌株丧失菌核形成能力,Δcit1菌株在YES培养基中的AFB1合成量减少。同时,cit1菌株在玉米种子上的致病性显著减弱。总之,cit1是黄曲霉菌核形成的关键基因,参与黄曲霉生长发育、毒素合成、致病性等生物过程。

关键词: 黄曲霉, 黄曲霉毒素, cit1基因, 柠檬酸合酶

Abstract: Aflatoxin B1 (AFB1), a highly carcinogenic secondary metabolite produced byAspergillus flavus, poses a serious threat to human health and agricultural economic development. CIT, a citrate synthase encoded by thecit1gene inA. flavus, catalyzes the condensation of acetyl-CoA and oxaloacetate to form citrate in the first step of the tricarboxylic acid (TCA) cycle, which is involved in the regulation of eukaryotic development, cell apoptosis, and cancer cell proliferation. To provide new insights for effective prevention and control ofA. flavus,the functions of Cit1 were explored in this study. Bioinformatics analysis indicated thatA. flavusCit1 displayed high similarity to orthologs from otherAspergillusspecies. The deletion ofcit1was constructed using homologous recombination methodology. Phenotypic assays and qRT-PCR analysis indicated that the deletion ofcit1affectedA. flavusdevelopment and pathogenicity. The colony diameter of the Δcit1strain was significantly reduced, and the conidial number and morphology in Δcit1differed from those of the wild type (WT) strain. Sclerotial formation was disrupted in Δcit1. Moreover, AFB1 production in Δcit1was decreased. Pathogenicity toward maize kernels in Δcit1was sharply attenuated compared with that of WT. Collectively, thecit1gene was crucial for sclerotial formation, and was also involved in various biological processes includingA. flavusvegetative growth, aflatoxin biosynthesis, and pathogenicity.

Key words: Aspergillus flavus, aflatoxin;cit1gene, citrate synthase

中图分类号: