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作 者:王志新[1] 蔡宇杰[1] 廖祥儒[1] 钱丽园[1] 张大兵[2]
机构地区:[1]江南大学工业生物技术教育部重点实验室 [2]江苏汉邦科技有限公司,江苏淮安223001
出 处:《食品与发酵工业》2009年第8期5-10,共6页Food and Fermentation Industries
基 金:长江学者和创新团队发展计划资助(No.:IRT0532)
摘 要:从朽木上筛选到一株产漆酶的白腐真菌SYBC-L1,该菌株在PDA-Guaiacol培养基上显红色,通过18S rDNA序列测定和进化树聚类分析,表明其属于密孔菌属,命名为Pycnoporus sp. SYBC-L1。以水葫芦为基本培养基质,以漆酶活力为指标,对其产酶培养基进行了初步优化,得其适宜的培养基为:水葫芦12.5%,可溶性淀粉与豆粕质量比1∶1,起始含水量65%,Cu2+浓度1.5mmol/L,没食子酸20μmol/L,30℃,培养9d,漆酶活力可达19.17U/g,为优化前的8.75倍。Pycnoporus sp. SYBC-L1漆酶提取的适宜条件为:20mmol/L,pH6.0的磷酸盐-柠檬酸缓冲液,浸提3h。A new laccase - producing fungus SYBC-L1 was isolated from a rotten wood. The strain appeared red color around the margin of colonies on PDA-Guaiacol plate. According to the 18S rDNA sequence analysis, the strain SYBC -L1 was proved to belong to genus Pycnoporus and identified as Pycnoporus sp. SYBC -L1. The laccase producing factors of Pycnoporus sp. SYBC-L1 was optimized by using solid - state fermentation. The results showed the optimal medium was as follows: hyacinth 12.5% , soluble starch and soybean meal with a ratio of 1:1, water content 65% , Cu2. 1.5 mmol/L and gallic acid 20 μmol/L. After 9 days of cultivation at 30 ℃ , the maximum laccase activity was determined to be 19.17 U/g, which was 8.75 folds than that in basal medium. The laccase of Pycnoporus sp. SYBC-L1 was extracted with citrate/Na2HPO4 buffer (20 mmol/L, pH 6.0) for 3 h.
关 键 词:Pycnoporus sp.SYBC—L1 18S rDNA 漆酶 水葫芦 固态发酵
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