生物技术
生物技術
생물기술
BIOTECHNOLOGY
2010年
2期
25-27
,共3页
真菌遗传%伞菌%物种%菌株%DNA指纹%遗传多样性%系统发育关系%种质鉴定
真菌遺傳%傘菌%物種%菌株%DNA指紋%遺傳多樣性%繫統髮育關繫%種質鑒定
진균유전%산균%물충%균주%DNA지문%유전다양성%계통발육관계%충질감정
Lentinula edodes%Pleurotus ostreatus%DNA fingerprinting%basidiocarps%mycelia%genetic identification
目的:伞菌物种以子实体形态特征为分类依据,研究以菌丝体代替子实体进行种质资源鉴定的遗传证据.方法:以常见的食用伞菌香菇、平菇子实体的不同部位组织及其分离菌丝体为供试材料,制备了12个随机引物介导的RAPD-PCR指纹,把DNA指纹图谱转化为简易的序列数据,经生物信息处理软件比较分析.结果:香菇不同菌株子实体DNA相似性系数在0.886~0.986之间,平菇不同菌株子实体DNA相似系数在0.779-0.976之间.对于供试的单个子实体而言,香菇和平菇子实体的菌盖、菌褶、菌柄及其组织分离菌丝体,与以此为菌种栽培得到的子实体相比较,所获得的有限DNA指纹图谱全部相同.结论:揭示了香菇和平菇不同菌株的遗传多样性,初步反映了伞菌不同发育阶段在分子水平上的遗传变异和亲缘关系,争论了以菌丝体代替子实体使厢RAPD手段进行种质资源鉴定与系统发育分析引出的真菌遗传问题.
目的:傘菌物種以子實體形態特徵為分類依據,研究以菌絲體代替子實體進行種質資源鑒定的遺傳證據.方法:以常見的食用傘菌香菇、平菇子實體的不同部位組織及其分離菌絲體為供試材料,製備瞭12箇隨機引物介導的RAPD-PCR指紋,把DNA指紋圖譜轉化為簡易的序列數據,經生物信息處理軟件比較分析.結果:香菇不同菌株子實體DNA相似性繫數在0.886~0.986之間,平菇不同菌株子實體DNA相似繫數在0.779-0.976之間.對于供試的單箇子實體而言,香菇和平菇子實體的菌蓋、菌褶、菌柄及其組織分離菌絲體,與以此為菌種栽培得到的子實體相比較,所穫得的有限DNA指紋圖譜全部相同.結論:揭示瞭香菇和平菇不同菌株的遺傳多樣性,初步反映瞭傘菌不同髮育階段在分子水平上的遺傳變異和親緣關繫,爭論瞭以菌絲體代替子實體使廂RAPD手段進行種質資源鑒定與繫統髮育分析引齣的真菌遺傳問題.
목적:산균물충이자실체형태특정위분류의거,연구이균사체대체자실체진행충질자원감정적유전증거.방법:이상견적식용산균향고、평고자실체적불동부위조직급기분리균사체위공시재료,제비료12개수궤인물개도적RAPD-PCR지문,파DNA지문도보전화위간역적서렬수거,경생물신식처리연건비교분석.결과:향고불동균주자실체DNA상사성계수재0.886~0.986지간,평고불동균주자실체DNA상사계수재0.779-0.976지간.대우공시적단개자실체이언,향고화평고자실체적균개、균습、균병급기조직분리균사체,여이차위균충재배득도적자실체상비교,소획득적유한DNA지문도보전부상동.결론:게시료향고화평고불동균주적유전다양성,초보반영료산균불동발육계단재분자수평상적유전변이화친연관계,쟁론료이균사체대체자실체사상RAPD수단진행충질자원감정여계통발육분석인출적진균유전문제.
Objective:DNA homogeneity in the edible fungi was studied to identify genetic relationship between basidioearps and their my-celia from gill fungi.Method :The DNA fingerprintings were compared mulually among different tissues of basidiocarps and their mycelial isolates of Lentinula edodes and Pleurotus ostreatus mushrooms in the studies.Result:The results showed that them were same DNA finger-printing patterns among pileus(including lamellae), lamellae, and stipe from one Lentinula edodes or Pleurotus ostreatus basidiocarp, and between the mycelial isolates and their original carpophores.However, there were a little DNA variation among basidiocarps of different source, and their similarity coefficients varied from 0.886 to 0.986 for Lentinula edodes mushrooms tested, and from 0.779 to 0.976 for Pleurotus ostreatus mushrooms tested with different colors and source.Conclusion:The RAPD(Random Amplified Polymorphic DNA) -PCR analyses using 12 arbitrary decamer nucleotide primers demonstrated that there exists DNA homogeneity in the edible fungi Lentinula edodes and Pleurotus ostreatus mushrooms, which provides the genetic basis for mycelial isolates identification by DNA fingerprinting com-parison between isolates and their original carpophores.The results also indicated that Lentinula edodes mushrooms tested and their myceli-al spawn kept the constant DNA fingerprinting patterns in the ins and outs of cultivation.