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基于核糖体大亚基rDNA序列鉴定药用蘑菇种类。

Identification of medicinal mushroom species based on nuclear large subunit rDNA sequences.

作者信息

Lee Ji Seon, Lim Mi Ok, Cho Kyoung Yeh, Cho Jung Hee, Chang Seung Yeup, Nam Doo Hyun

机构信息

Institute of Biotechnology, College of Pharmacy, Yeungnam University, Gyongsan 712-749, Republic of Korea.

出版信息

J Microbiol. 2006 Feb;44(1):29-34.

Abstract

The purpose of this study was to develop molecular identification method for medical mushrooms and their preparations based on the nucleotide sequences of nuclear large subunit (LSU) rDNA. Four specimens were collected of each of the three representative medicinal mushrooms used in Korea: Ganoderma lucidum, Coriolus versicolor, and Fomes fomentarius. Fungal material used in these experiments included two different mycelial cultures and two different fruiting bodies from wild or cultivated mushrooms. The genomic DNA of mushrooms were extracted and 3 nuclear LSU rDNA fragments were amplified: set 1 for the 1.1-kb DNA fragment in the upstream region, set 2 for the 1.2-kb fragment in the middle, and set 3 for the 1.3-kb fragment downstream. The amplified gene products of nuclear large subunit rDNA from 3 different mushrooms were cloned into E. coli vector and subjected to nucleotide sequence determination. The sequence thus determined revealed that the gene sequences of the same medicinal mushroom species were more than 99.48% homologous, and the consensus sequences of 3 different medicinal mushrooms were more than 97.80% homologous. Restriction analysis revealed no useful restriction sites for 6-bp recognition enzymes for distinguishing the 3 sequences from one another, but some distinctive restriction patterns were recognized by the 4-bp recognition enzymes AccII and HhaI. This analysis was also confirmed by PCR-RFLP experiments on medicinal mushrooms.

摘要

本研究的目的是基于核糖体大亚基(LSU)rDNA的核苷酸序列,开发用于药用蘑菇及其制剂的分子鉴定方法。采集了韩国使用的三种代表性药用蘑菇的标本各4份:灵芝、云芝和木蹄层孔菌。这些实验中使用的真菌材料包括两种不同的菌丝体培养物以及野生或栽培蘑菇的两种不同子实体。提取蘑菇的基因组DNA,并扩增3个核糖体大亚基rDNA片段:上游区域1.1kb DNA片段的第1组、中间1.2kb片段的第2组以及下游1.3kb片段的第3组。将来自3种不同蘑菇的核糖体大亚基rDNA的扩增基因产物克隆到大肠杆菌载体中,并进行核苷酸序列测定。所测定的序列表明,同一药用蘑菇物种的基因序列同源性超过99.48% , 3种不同药用蘑菇的共有序列同源性超过97.80%。限制性酶切分析显示,对于区分这3个序列的6bp识别酶没有有用的限制性酶切位点,但4bp识别酶AccII和HhaI识别出了一些独特限制性酶切模式。对药用蘑菇的PCR-RFLP实验也证实了这一分析结果。

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