摘要
采用培养特征观察,竹红菌甲素测定和分子生物学等技术和方法,研究了不同培养基上竹黄菌的生物量,产竹红菌素甲素和形成子座情况,结果表明,葡萄糖20g,琼脂20g,竹汁1000mL(竹枝200g煮沸取滤液),pH自然的培养基中并插入灭菌的竹枝,接入竹黄菌种,7d后,该培养基上菌丝生物量和其竹红菌素量均为最高,且约6个月室内室温(0~20℃)培养获得了类天然竹黄状的培养物,该培养物经过了竹红菌甲素测定及分子鉴定分析多途径的综合验证。通过本实验,竹黄无性型菌的人工培养取得一定进展。
The biomass,hypocrellin A and forming fruit body of Shiraia bambusicola on the different medias were explored. Through the method of culture characters,hypocrellin A determination and molecular biology,the results showed that mycielia biomass and hypocrellin A were the best on the medium consisting of glucose 20g, agar 20g, bamboo filter liquor(bamboo pole 200g boiled) 1000mL, and inserted sterile bumboo poles ; And on above medium,S, bambusicola-like fruit bodies were obtained when the strain were inoculated and cultivated under the room temperature (0-20℃) lasting six months. S. bambusicola-like fruit bodies were confirmed by hypocrellin A determination and molecular identification. The experiments showed that the fruit body of S. bambusicola on artificial culture made progress.
出处
《食品工业科技》
CAS
CSCD
北大核心
2012年第14期239-241,249,共4页
Science and Technology of Food Industry
基金
国家自然科学基金项目(30960004)
贵州省自然科学基金项目[黔科合字(2008)2266号]
贵州大学引进人才科研项目[贵大人基合字(2007)035号]
关键词
竹黄菌
竹黄子实体
人工培养
竹红菌素
分子鉴定
Shiraia bambusicola
fruitbody
artificial culture
hypocrellin a
molecular identification