期刊文献+

榆黄菇优良新菌株的选育 被引量:3

Breeding of A Novel Pleurotus citrinopileatus Strain
下载PDF
导出
摘要 为研究60Co-γ射线对榆黄菇菌丝遗传诱变的影响,采用不同的辐照剂量和不同的辐照剂量率对出发菌株榆黄菇818的尖端菌丝进行辐照处理。结果表明:在辐照剂量为600Gy、辐照剂量率为43.5Gy/h的条件下,菌丝再生后进行挑选,获得了生长优良的诱变菌株。将诱变菌株与出发菌株进行生长对比实验,诱变菌株菌丝生长速度平均提高21.1%;经拮抗实验、酯酶和过氧化物酶同工酶实验,证明诱变菌株遗传物质发生了变化,已不同于出发菌株,具有种的特异性;经连续转接6代进行固体培养,诱变菌株优良的生长性能得到了保持,具有遗传稳定性。 The effect of 60Co-γ irradiation with different doses and dose rates on mycelial growth of Pleurotus citrinopileatus was investigated in this study. Mutant strains of Pleurotus citrinopileatus with high growth rate were obtained through 60Co-γ irradiation at 600 Gy and 43.5 Gy/h dose rate. After the regeneration of mycelia, a novel strain having the highest growth rate was screened, which showed an average increase of 21.1% when compared with that of the parental strain. Results of antagonistic test, esterase isozyme and peroxidase isozyme eleetrophoresis revealed significant genetic differences between the mutant strain and its parent stain. After six generations of continuous cultivation, the mutant strain kept the good growth vigor, thereby displaying high genetic stability.
出处 《食品科学》 EI CAS CSCD 北大核心 2009年第21期301-304,共4页 Food Science
基金 山东省农业良种工程项目(鲁科农字[2005]99号) 山东省教育厅科技计划项目(J06N02) 鲁东大学人才基金项目(LY20063303) 鲁东大学创新团队建设项目
关键词 榆黄菇 诱变 选育 Pleurotus citrinopileatus mutagenesis breeding
  • 相关文献

参考文献8

二级参考文献46

共引文献78

同被引文献25

  • 1王香兰,刘淑芳,姜德凯,周学政,蔡德华,张秋胜.榆黄菇的三种高产栽培模式比较研究[J].中国食用菌,2009,28(3):67-68. 被引量:7
  • 2SONG Zhenqiao, LI Xingfeng, WANG Honggang, et al. Genetic diver-sity and population structure of Salvia miltiorrhiza Bge in China revealed by ISSR and SRAP[J]. Genetica, 2010, 138(2): 241-249. 被引量:1
  • 3NAGARAJU J, KATHIRVEL M, KUMAR RR, et al. Genetic analysis of traditional and evolved Basmati and non-Basmati rice varieties by using fluorescence-based ISSR-PCR and SSR markers[J] Pmceedinds of the National Academy of Sciences of the United States of America, 2002, 99(9): 5836-5841. 被引量:1
  • 4MAHMUDUL I N, BIAN Yinbing. ISSR as new markers for identifica-tion of homokaryotic protoclones ofAgaricus bisporus[J]. Curr Microbiol, 2010, 60(2): 92-98. 被引量:1
  • 5van ELSAS J D, DUARTE G F, KEIJZER-WOLTERS A, et al. Analy-sis of the dynamics of fungal communities in soil via fungal-specific PCR of soil DNA followed by denaturing gradient gel electrophoresis[J]. Journal of Microbiological Methods, 2000, 43(2): 133-151. 被引量:1
  • 6PILOTFI C A, SANDERSON F R, AITKEN E A B, et al. Morphologi-cal variation and host range of two Ganoderma species from Papua New Guinea[J]. Mycopathologia, 2004, 158(2): 251-265. 被引量:1
  • 7KOMON-ZELAZOWSKA M, BISSETr J, ZAFARI D, et al. Geneti-cally closely related but phenotypically divergent Trichoderma species cause green mold disease in oyster mushroom farms worldwide[J]. Appl Environ Microbiol, 2007, 73(22): 7415-7426. 被引量:1
  • 8QIN Lianhua, TAN Qi, CHEN Mingjie, et al. Use of intersimple se-quence repeatsmarkers to develop strain-specific SCARmarkers for Lentinula edodes[J]. FEMS Microbiol Lett, 2006, 257(1): 112-116. 被引量:1
  • 9宋小亚,肖扬,边银丙.ISSR标记在黑木耳单核体遗传分析中的应用[J].菌物学报,2007,26(4):528-533. 被引量:28
  • 10王波,彭卫红,甘炳成.金针菇33个菌株遗传多样性与组织分离菌株鉴定的酯酶同工酶分析[J].西南农业学报,2008,21(2):448-450. 被引量:22

引证文献3

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部