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六盘山药用桑黄分离鉴定与培养研究OA

Study on Isolation,Identification and Cultivation of Sanghuangporus sanghuang from Liupanshan

中文摘要英文摘要

[目的]依托六盘山优质山地生态资源,开展野生桑黄种质资源挖掘,系统研究目标菌株生物学特性,筛选菌丝生长最适培养条件.[方法]以六盘山国家级自然保护区采集的野生桑黄子实体为试验材料,采用组织分离法纯化获得菌株S-1;利用ITS序列开展分子系统鉴定,通过单因素试验明确菌丝最适培养条件,同步优化母种、原种、栽培种三级培养基配方.[结果]经形态特征观察结合ITS序列分子鉴定,判定分离菌株S-1为火木层孔菌(Phellinus igniarius);该菌株菌丝体生长的最适碳源、氮源、无机盐分别为蔗糖、酵母浸粉、硫酸铁,最适培养温度25℃;最优母种培养基为麦粒基质,最优原种培养基为杂木屑基质,最优栽培种培养基为木屑麦麸复合基质.[结论]分离纯化得到六盘山野生火木层孔菌菌株S-1,明确了该菌株菌丝生长最优培养条件与三级菌种配套培养基配方,可为六盘山野生桑黄人工驯化、规模化栽培及种质资源开发提供菌种依据与标准化培养技术参考.

[Objective]Relying on the high-quality mountain ecological resources of Liupanshan,this study excavated Sanghuang spp.germplasm resources,systematically investigated the biological characteristics of the target strain,and screend the optimal culture conditions for mycelial growth.[Method]Using Sanghuang spp.fruiting bodies collected from Liupanshan National Nature Reserve as experimental materials,strain S-1 was obtained and purified via tissue isolation;molecular phylogenetic identification was performed based on ITS sequences,the optimal culture conditions for mycelia were determined through single-factor experiments,and the formulas of three-stage culture media for mother culture,original culture and cultivation culture were optimized synchronously.[Result]Combining morphological observation and molecular identification based on ITS sequences,the isolated strain S-1 was identified as Phellinus igniarius.The optimal carbon source,nitrogen source and inorganic salt for mycelial growth of this strain were sucrose,yeast extract powder and ferric sulfate respectively,and the optimal culture temperature was 25℃.The optimal medium for mother culture was wheat grain substrate,the optimal medium for original culture was miscellaneous sawdust substrate,and the optimal medium for cultivation culture was sawdust and wheat bran composite substrate.[Conclusion]The wild Phellinus igniarius strain S-1 was isolated and purified from Liupanshan,and the optimal culture conditions for mycelial growth and the matching three-stage medium formula of this strain were clarified.This study can provide bacterial strain basis and standardized culture technical reference for artificial domestication,large-scale cultivation and germplasm resource development of Sanghuang spp.in Liupanshan.

李颖;王正安;贾宝光;朱金霞

宁夏农林科学院固原分院,宁夏 固原 756000宁夏农林科学院固原分院,宁夏 固原 756000宁夏农林科学院固原分院,宁夏 固原 756000宁夏农林科学院农业生物技术研究中心,宁夏 银川 750002

农业科技

野生桑黄分离鉴定培养六盘山

LiupanshanSanghuang spp.Isolation and identificationCulture

《宁夏农林科技》 2026 (7)

66-73,8

宁夏重点研发项目(2022BBF03027)、宁夏农林科学院对外科技合作项目(DW-X-2022001)、宁夏农林科学院对外合作专项(DW-X-2020007-5)、宁夏科技基础条件建设专项(2022DPC05001).

10.3969/j.issn.1002-204x.2026.07.009

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