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康氏木霉纤维素酶CBHI基因克隆及在大肠杆菌中的表达 被引量:7
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作者 黄时海 康超 +7 位作者 黄飞 曹喜秀 何鑫平 汪晟 吴孔阳 曹普美 梁智群 李湘萍 《中国酿造》 CAS 北大核心 2011年第2期76-80,共5页
将康氏木霉(Trichoderma koningii)总RNA反转录成cDNA第一链,并以之为模板进行RT-PCR,合成约1.5kb的纤维二糖水解酶Ⅰ(cbh I)基因。cbhI基因经测序确认后克隆到表达载体pET-30a(+)上,PCR和双酶切鉴定筛选阳性重组子;将阳性质粒转化大肠... 将康氏木霉(Trichoderma koningii)总RNA反转录成cDNA第一链,并以之为模板进行RT-PCR,合成约1.5kb的纤维二糖水解酶Ⅰ(cbh I)基因。cbhI基因经测序确认后克隆到表达载体pET-30a(+)上,PCR和双酶切鉴定筛选阳性重组子;将阳性质粒转化大肠杆菌BL21(DE3)plysS,并用0.4mmol/L的IPTG诱导表达重组蛋白。实验结果:cbh I基因在BL21(DE3)plysS中胞内融合表达,重组蛋白pNPC酶活为15.6U/L,最适反应温度为45℃,最适pH值为5.0,Mn2+对酶活力有明显的促进作用,SDS-PAGE表明重组蛋白分子量约为70kDa。 展开更多
关键词 康氏木霉 纤维二糖水解酶I cbhI基因 克隆表达
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Designing a SCAR molecular marker for monitoring Trichoderma cf. harzianum in experimental communities
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作者 Gabriel PéREZ Valentina VERDEJO +2 位作者 Clarissa GONDIM-PORTO Julieta ORLANDO Margarita CARú 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2014年第11期966-978,共13页
Several species of the fungal genus Trichoderma establish biological interactions with various micro- and macro-organisms. Some of these interactions are relevant in ecological terms and in biotechnological applicatio... Several species of the fungal genus Trichoderma establish biological interactions with various micro- and macro-organisms. Some of these interactions are relevant in ecological terms and in biotechnological applications, such as biocontrol, where Trichoderma could be considered as an invasive species that colonizes a recipient community. The success of this invasion depends on multiple factors, which can be assayed using experimental communities as study models. Therefore, the aim of this work is to develop a species-specific sequence-characterized amplified region (SCAR) marker to monitor the colonization and growth of T. cf. harzianum when it invades experi- mental communities. For this study, 16 randomly amplified polymorphic DNA (RAPD) primers of 10-mer were used to generate polymorphic patterns, one of which generated a band present only in strains of T. cf. harzianum. This band was cloned, sequenced, and five primers of 20-23 mer were designed. Primer pairs 2F2/2R2 and 2F2/2R3 successfully and specifically amplified fragments of 278 and 448 bp from the T. cf. harzianum BpT10a strain DNA, respectively. Both primer pairs were also tested against the DNA from 14 strains of T. cf. harzianum and several strains of different fungal genera as specificity controls. Only the DNA from the strains of T. cf. hat-zianum was successfully amplified. Moreover, primer pair 2F2/2R2 was assessed by quantitative real-time polymerase chain reaction (PCR) using fungal DNA mixtures and DNA extracted from fungal experimental communities as templates. T. cf. harzianum was detectable even when as few as 100 copies of the SCAR marker were available or even when its population represented only 0.1% of the whole community. 展开更多
关键词 tnchoderma cf. harzianum Sequence-characterized amplified region (SCAR) Molecular marker Experimental fungal communities
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