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靓丽乳菇菌丝高效扩增培养的方法
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作者 孙举志 陈菲菲 +2 位作者 李红英 向全 杨永康 《中国食用菌》 2022年第9期40-43,47,共5页
菌根类食用菌的菌丝生长缓慢,生物量低,难以培养,对人工合成菌根苗以及仿野生人工栽培造成了困难。将分离得到的靓丽乳菇菌丝经组织破碎仪破碎后再接种至固体培养基上培养的方法,相比传统截取尖端菌丝转接培养的方法,具有培养周期短、... 菌根类食用菌的菌丝生长缓慢,生物量低,难以培养,对人工合成菌根苗以及仿野生人工栽培造成了困难。将分离得到的靓丽乳菇菌丝经组织破碎仪破碎后再接种至固体培养基上培养的方法,相比传统截取尖端菌丝转接培养的方法,具有培养周期短、生长速度快、生物量大等优点。传统培养方法下,菌落直径为6.60 cm,菌丝干质量为0.05 g,生长时间为63 d,生长速度为0.10 cm·d^(-1),基质菌丝发达,气生菌丝弱。经组织破碎再培养,其菌落直径达7.55 cm,菌丝干质量达0.27 g,生长时间为29 d,生长速度达0.26 cm·d^(-1),基质菌丝和气生菌丝都很发达。与传统方法相比较,菌丝生长速度提高160%,干质量增加440%,生长时间缩短54%。该方法培养靓丽乳菇菌丝具有稳定、快捷、高效的优点,为菌根苗前期的菌丝纯培养以及其他外生菌根类真菌的研究提供了借鉴和参考。 展开更多
关键词 靓丽乳菇 菌根真菌 菌丝扩增
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Selection of a DNA barcode for Nectriaceae from fungal whole-genomes 被引量:6
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作者 ZENG ZhaoQing ZHAO Peng +2 位作者 LUO Jing ZHUANG WenYing YU ZhiHe 《Science China(Life Sciences)》 SCIE CAS 2012年第1期80-88,共9页
A DNA barcode is a short segment of sequence that is able to distinguish species. A barcode must ideally contain enough variation to distinguish every individual species and be easily obtained. Fungi of Nectriaceae ar... A DNA barcode is a short segment of sequence that is able to distinguish species. A barcode must ideally contain enough variation to distinguish every individual species and be easily obtained. Fungi of Nectriaceae are economically important and show high species diversity. To establish a standard DNA barcode for this group of fungi, the genomes of Neurospora crassa and 30 other filamentous fungi were compared. The expect value was treated as a criterion to recognize homologous sequences. Four candidate markers, Hsp90, AAC, CDC48, and EF3, were tested for their feasibility as barcodes in the identification of 34 well-established species belonging to 13 genera of Nectriaceae. Two hundred and fifteen sequences were analyzed. Intraand inter-specific variations and the success rate of PCR amplification and sequencing were considered as important criteria for estimation of the candidate markers. Ultimately, the partial EF3 gene met the requirements for a good DNA barcode: No overlap was found between the intra-and inter-specific pairwise distances. The smallest inter-specific distance of EF3 gene was 3.19%, while the largest intra-specific distance was 1.79%. In addition, there was a high success rate in PCR and sequencing for this gene (96.3%). CDC48 showed sufficiently high sequence variation among species, but the PCR and sequencing success rate was 84% using a single pair of primers. Although the Hsp90 and AAC genes had higher PCR and sequencing success rates (96.3% and 97.5%, respectively), overlapping occurred between the intraand inter-specific variations, which could lead to misidentification. Therefore, we propose the EF3 gene as a possible DNA barcode for the nectriaceous fungi. 展开更多
关键词 barcoding gap expect value fungal genomes homologous sequence PCR and sequencing success rate sequence variation
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