食用菌学报
食用菌學報
식용균학보
ACTA EDULIS FUNGI
2014年
2期
25-31
,共7页
邓优锦%王庆福%陈介斌%苏婉真%谢宝贵
鄧優錦%王慶福%陳介斌%囌婉真%謝寶貴
산우금%왕경복%진개빈%소완진%사보귀
香灰菌%RAPD%SRAP%ISSR
香灰菌%RAPD%SRAP%ISSR
향회균%RAPD%SRAP%ISSR
Xiang-hui-jun%RAPD%SRAP%ISSR
香灰菌(xiang-hui-jun)是银耳(Tremella fuciformis)的伴生菌,对银耳的生长、发育具有至关重要的作用。采用 RAPD、SRAP 和 ISSR 三种分子标记对具有拮抗关系的18个香灰菌菌株进行遗传差异性分析。结果表明:8对 RAPD 引物共扩增出59个位点片段,多态性条带总共为49条,占总片段条数的比率为83%;7对 SRAP 引物共扩增出49个位点片段,多态性条带总共为47条,占总片段条数的比率为96%;6对 ISSR 引物共扩增出60个位点片段,多态性条带总共为50条,占总片段条数的比率为83%。聚类分析表明,当以相异系数0.48为阈值时,可将这些香灰菌株分成7个类群:Hp.sp0006、TR 柏溪、瓦坑野生、TR 枫树和 TR8801枫树分别自成一个类群,Hp.sp0052和69为一个类群,其余11个(Hp.sp0004、Hp.sp0010、T0050、T0048、T0036、TR23、TR5、TR95、71、TR03和 TR86)菌株归为一个类群。
香灰菌(xiang-hui-jun)是銀耳(Tremella fuciformis)的伴生菌,對銀耳的生長、髮育具有至關重要的作用。採用 RAPD、SRAP 和 ISSR 三種分子標記對具有拮抗關繫的18箇香灰菌菌株進行遺傳差異性分析。結果錶明:8對 RAPD 引物共擴增齣59箇位點片段,多態性條帶總共為49條,佔總片段條數的比率為83%;7對 SRAP 引物共擴增齣49箇位點片段,多態性條帶總共為47條,佔總片段條數的比率為96%;6對 ISSR 引物共擴增齣60箇位點片段,多態性條帶總共為50條,佔總片段條數的比率為83%。聚類分析錶明,噹以相異繫數0.48為閾值時,可將這些香灰菌株分成7箇類群:Hp.sp0006、TR 柏溪、瓦坑野生、TR 楓樹和 TR8801楓樹分彆自成一箇類群,Hp.sp0052和69為一箇類群,其餘11箇(Hp.sp0004、Hp.sp0010、T0050、T0048、T0036、TR23、TR5、TR95、71、TR03和 TR86)菌株歸為一箇類群。
향회균(xiang-hui-jun)시은이(Tremella fuciformis)적반생균,대은이적생장、발육구유지관중요적작용。채용 RAPD、SRAP 화 ISSR 삼충분자표기대구유길항관계적18개향회균균주진행유전차이성분석。결과표명:8대 RAPD 인물공확증출59개위점편단,다태성조대총공위49조,점총편단조수적비솔위83%;7대 SRAP 인물공확증출49개위점편단,다태성조대총공위47조,점총편단조수적비솔위96%;6대 ISSR 인물공확증출60개위점편단,다태성조대총공위50조,점총편단조수적비솔위83%。취류분석표명,당이상이계수0.48위역치시,가장저사향회균주분성7개류군:Hp.sp0006、TR 백계、와갱야생、TR 풍수화 TR8801풍수분별자성일개류군,Hp.sp0052화69위일개류군,기여11개(Hp.sp0004、Hp.sp0010、T0050、T0048、T0036、TR23、TR5、TR95、71、TR03화 TR86)균주귀위일개류군。
Genetic diversity among 18 antagonistic strains of Xiang-hui-jun,the cohabitant fungus of Tremella fuciformis that plays a vital role in the growth and development of the mushroom,was analyzed using randomly amplified polymorphic DNA (RAPD),sequence-related amplified polymorphism(SRAP)and inter-simple sequence repeat (ISSR)markers.Eight RAPD primers generated 59 DNA bands from the 18 strains of which 49 (83%)were polymorphic,seven SRAP primers generated 49 DNA bands of which 47 (96%)were polymorphic,while six ISSR primers generated 60 DNA bands of which 50 (83%)were polymorphic.A dendrogram based on RAPD、ISSR and RAPD analyses was constructed using the unweighted pair-group method with arithmetic means,and the 18 strains were delineated into seven groups at a dissimilarity coefficient level of 0.48 as follows:strains Hp.sp0006,TR Boxi,Wakeng wild,TR Fengshu and TR8801 Fengshu each constituted individual groups (Groups 1-5),Group 6 comprised strains Hp.sp0052 and 69,and the remaining 11 strains (Hp.sp0004,Hp.sp0010,T0050,T0048,T0036,TR23,TR5,TR95,71,TR03 and TR86)clustered together to form Group 7.