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香梨果萼黑斑病菌Alternaria alternata遗传转化体系的建立及GFP标记菌株的获得
Development of efficient genetic transformation system in Alternaria alternata and its application for strain labeled with GFP

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文摘 为建立香梨果萼黑斑病菌链格孢(Alternaria alternata)的原生质体遗传转化体系,本实验以香梨果萼黑斑病菌强致病性菌株LI1为供试材料,研究菌龄、酶系统、酶解时间等对链格孢菌原生质体制备的影响。链格孢菌菌丝在CM液体培养基中培养20 h,以0.7 mol·L~(-1) NaCl为稳渗剂,1%裂解酶+1%崩溃酶+1%蜗牛酶的酶液组合下,28 ℃酶解4 h,原生质体制备效率最高。通过PEG / CaCl_2介导法将含有潮霉素B抗性基因和绿色荧光蛋白基因的质粒转入链格孢菌LI1,转化子生长表型及外源基因的PCR鉴定结果表明抗性基因已成功整合到香梨果萼黑斑病菌中。成功建立了香梨果萼黑斑病菌链格孢菌的原生质体遗传转化体系,并成功获得GFP标记菌株,为病原菌侵染定殖过程及致病机制研究奠定了基础。
其他语种文摘 In this study, we aimed to develop an efficient protoplast transformation system in Alternaria alternata. Several main parameters for isolation of protoplasts, such as the mycelial age, enzyme system, and digesting time, were analyzed and optimized for the strain LI1 of A. alternata with strong pathogenicity. The combined conditions for highest efficiency of protoplast isolation for LI1 strain were as below: the mycelia cultured in CM liquid medium for 20 hours, 0.7 mol·L~(-1) NaCl as the osmotic stabilizer, enzyme mixture including 1% Driselase, 1% Lysing enzyme and 1% Snailase for 4 hours of incubation with the mycelia at 28 ℃ at 110 r·min~(-1). Moreover, the regeneration of protoplasts was tested with transformation of the plasmid pCT74 DNA containing GFP reporter and the Hyg B resistant genes into LI1 by using PEG / CaCl_2-mediated method. The following confirmation of transformants by PCR and growth phenotypes indicated that the GFP gene was successfully integrated into the LI1 strain genome. In summary, we successfully developed the protoplast transformation system and generated the GFP transgenic strain of A. alternata, which would benefited for understanding of the infection, host colonization, and pathogenic mechanism of this fungus.
来源 植物病理学报 ,2022,52(1):97-103 【核心库】
DOI 10.13926/j.cnki.apps.000491
关键词 香梨果萼黑斑病 ; 链格孢 ; 原生质体 ; 遗传转化
地址

1. 新疆农业科学院植物保护研究所, 农业部西北荒漠作物有害生物综合治理重点实验室, 乌鲁木齐, 830091  

2. 新疆农业大学林学与园艺学院, 乌鲁木齐, 830052  

3. 新疆农业科学院微生物应用研究所, 乌鲁木齐, 830091  

4. 库尔勒市香梨研究中心, 库尔勒, 841000

语种 中文
文献类型 研究性论文
ISSN 0412-0914
学科 植物保护
基金 新疆维吾尔自治区自然科学基金
文献收藏号 CSCD:7233873

参考文献 共 23 共2页

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引证文献 2

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2 赵楠 深色有隔内生真菌S12菌株遗传转化体系的建立及GFP标记菌株的获得 西北农林科技大学学报. 自然科学版,2024,52(4):127-135,145
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