[Establishment and optimization of Agrobacterium tumefaciens-mediated genetic transformation system for Polyporus umbellatus].

Q3 Pharmacology, Toxicology and Pharmaceutics
Li Chi, Peng-Jie Han, Hong-Hong Jiao, Tian-Rui Liu, Jun-Hui Zhou, Yuan Yuan
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引用次数: 0

Abstract

The unstable quality of Polyporus umbellatus sclerotia during cultivation is the key factor affecting the quality and yield of P. umbellatus sclerotia. In order to provide technical support for obtaining superior P. umbellatus by molecular breeding, the genetic transformation system mediated by Agrobacterium tumefaciens was studied in this paper. A. tumefaciens-mediated method was used to investigate the effects of antibiotic concentration, strain type, A. tumefaciens concentration, receptor material, infection time, co-culture time, and screening conditions on the genetic transformation efficiency of P. umbellatus. The transformants were screened and detected by hygromycin resistance marker genes, polymerase chain reaction(PCR) of specific primers, and fluorescence detection methods. The results showed that the A. tumefaciens GV3101 strain could genetically transfer P. umbellatus mycelium cells, and the optimal conditions for infection were as follows: the A. tumefaciens concentration A_(600 nm)= 0.6, P. umbellatus mycelium cells as receptor material, infection time of 30 min, and co-culture time of 3 days. The two-step screening method involving hygromycin of 9 and 13 μg·mL~(-1 )was the best screening condition. The results of hygromycin resistance screening, PCR detection of specific primers, and fluorescence detection showed that the exogenous gene eGFP had been transferred into the P. umbellatus mycelium cells, integrated into the genome, and successfully expressed. Under optimal conditions, the conversion efficiency could be increased to 2.3%, and the genetic transformation period was shortened from more than 90 days to less than 60 days. This study established and optimized the genetic transformation system of P. umbellatus mycelium cells mediated by A. tumefaciens, laying a foundation for the analysis of the molecular mechanism of P. umbellatus during growth and molecular breeding.

[建立和优化农杆菌介导的伞形多孔菌遗传转化系统]。
伞形多孔菌(Polyporus umbellatus)硬菌丝在栽培过程中质量不稳定是影响伞形多孔菌硬菌丝质量和产量的关键因素。为了给通过分子育种获得优良的伞形多孔菌提供技术支持,本文研究了农杆菌介导的遗传转化系统。采用农杆菌介导法研究了抗生素浓度、菌株类型、农杆菌浓度、受体材料、感染时间、共培养时间和筛选条件对伞形花序遗传转化效率的影响。通过土霉素抗性标记基因、特异引物聚合酶链式反应(PCR)和荧光检测等方法对转化子进行筛选和检测。结果表明,A. tumefaciens GV3101菌株能对伞菌菌丝体细胞进行基因转移,其最佳感染条件为:A. tumefaciens浓度A_(600 nm)=0.6,伞菌菌丝体细胞为受体材料,感染时间为30分钟,共培养时间为3天。用 9 和 13 μg-mL~(-1 )的潮霉素进行两步筛选法是最佳的筛选条件。通过对潮霉素抗性筛选、特异引物 PCR 检测和荧光检测的结果表明,外源基因 eGFP 已转入伞菌菌丝细胞,整合到基因组中并成功表达。在最佳条件下,转化效率可提高到 2.3%,遗传转化周期从 90 多天缩短到 60 天以内。该研究建立并优化了由瘤单胞菌介导的伞形花序菌丝体细胞遗传转化体系,为分析伞形花序生长过程中的分子机理和分子育种奠定了基础。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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