研究报告

桃红侧耳原生质体细胞融合选育高产菌丝蛋白菌株

  • 魏荷芬 ,
  • 潘晶 ,
  • 张健 ,
  • 温庆仕 ,
  • 刘庆国 ,
  • 唐成伦 ,
  • 周萍
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  • 1(南京高新工大生物技术研究院有限公司, 江苏 南京, 211800)
    2(江苏科技大学, 江苏 镇江, 212100)
    3(江苏集萃工业生物技术研究所有限公司, 江苏 南京, 211800)
    4(南京生命原健康科技有限公司, 江苏 南京, 211800)
第一作者:硕士,助理研究员(张健研究员和刘庆国副研究员为共同通信作者,E-mail:zjok0511@just.edu.cn;liuqg1987@126.com)

收稿日期: 2024-02-19

  修回日期: 2024-03-14

  网络出版日期: 2025-02-21

基金资助

江苏省青年科学基金项目(BK20210145)

A high-yield mycelial protein strain was selected by fusion of plasma cells of Pleurotus djamor

  • WEI Hefen ,
  • PAN Jing ,
  • ZHANG Jian ,
  • WEN Qingshi ,
  • LIU Qingguo ,
  • TANG Chenglun ,
  • ZHOU Ping
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  • 1(Nanjing Hi Tech University Biotechnology Research Institute Co. Ltd., Nanjing 211800, China)
    2(Jiangsu University of Science and Technology, Zhenjiang 212100, China)
    3(Jiangsu Institute of Industrial Biotechnology, JITRI Co. Ltd., Nanjing 211800, China)
    4(Nanjing Life Health Technology Co. Ltd., Nanjing 211800, China)

Received date: 2024-02-19

  Revised date: 2024-03-14

  Online published: 2025-02-21

摘要

随着人口的快速增长,全球范围内对优质蛋白质的需求日益增强,通过食用菌育种技术培育高产、高蛋白的优质菌株,将菌丝体蛋白用作新的蛋白质来源,可以缓解蛋白质短缺的问题。该研究以桃红侧耳GXGD-13-1为原始菌株,通过原生质体细胞融合技术,提高桃红侧耳菌丝体的蛋白质产量。菌丝体的细胞壁在组合酶M2中酶解3 h,释放的原生质体利用250 g/L的聚乙二醇为融合剂进行聚集融合,最终融合率达到53%,有效克服了桃红侧耳四极性的交配系统亲和率低的育种壁垒。融合再生后的菌株经过选育高产菌丝蛋白菌株的初筛和复筛,得到融合菌株R-1,经凯氏定氮仪测定,计算其菌丝体蛋白质产量比原始菌株GXGD-13-1提高约23%。该文的实验工作,证明了原生质体细胞融合育种技术对选育高产菌丝体蛋白质菌株的有效性,为满足不断增长的蛋白质需求提供新的有效途径。

本文引用格式

魏荷芬 , 潘晶 , 张健 , 温庆仕 , 刘庆国 , 唐成伦 , 周萍 . 桃红侧耳原生质体细胞融合选育高产菌丝蛋白菌株[J]. 食品与发酵工业, 2025 , 51(3) : 147 -153 . DOI: 10.13995/j.cnki.11-1802/ts.038896

Abstract

With the rapid growth of population, the global demand for high-quality protein is increasing day by day.To alleviate the problem of protein shortage, mycelium can be used as a new source of protein through the cultivation of high-quality strains of edible fungi breeding.In this study, Pleurotus djamor GXGD-13-1 was used as the original strain, protoplasmic cell fusion technique was used to increase its protein yield.First mycelium cell walls were enzymolysised in M2 composite for 3 hours, then released protoplast was fused with polyethylene glycol (PEG) in which 250 g/L of PEG was used as the fusion agent.A high fusion rate of 53% was achieved after the process, removing the breeding barrier of low compatibility of the tetrpolarity mating system.Primary screening and re-screening of fusion strain R-1 were carried out to select a high mycelial protein yield, 23% higher than that of the original strain GXGD-13-1.The work in this paper proved the efficiency of protoplasmic somatic cell fusion breeding technology in the selection of high-yield mycelium protein strains and provided an alternative way to meet the increasing demand for protein.

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