1.Characterization of a Septobasidium sp. Associated with Felt Disease of Schisandra chinensis.
In Young CHOI ; Wang Hyu LEE ; Jong Jin LEE ; Mi Jeong PARK ; Jeong Ae KO ; Jeong Ran CHOI ; Hyeon Dong SHIN
Mycobiology 2016;44(1):58-62
Extensive disease surveys performed during the summers of 2013 and 2014 in Schisandra chinensis orchards resulted in the finding of a Septobasidium sp. associated with felt disease. The fungus was characterized to be symbiotic with a scale insect (Pseudaulacaspis cockerelli). Morphological and molecular characteristics of the Septobasidium isolates were investigated. The isolates were morphologically and phylogenetically close to S. bogoriense. We tentatively describe this isolate as a Septobasidium sp., mainly because of the limited amount of information available on the internal transcribed spacer region of the ribosomal DNA of Septobasidium spp.
DNA, Ribosomal
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Fungi
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Hemiptera
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Schisandra*
2.Mycoflora and Enzymatic Characterization of Fungal Isolates in Commercial Meju, Starter for a Korean Traditional Fermented Soybean Product.
Jin Ho BAEK ; Kum Kang SO ; Yo Han KO ; Jung Mi KIM ; Dae Hyuk KIM
Mycobiology 2014;42(3):291-295
Mycoflora was assessed in the commercial meju from four well-separated geographic origins. A total of 112 fungal isolates were identified by phenotypic characteristics and molecular taxonomy using sequencing the internal transcribed spacer of the rDNA and revealed 19 species from 13 genera. Enzymatic characteristics of protease and amylase, and mycotoxin production were analyzed.
Amylases
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Classification
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DNA, Ribosomal
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Soybeans*
3.Phylogenetic Relationships of the Polyporaceae Based on Gene Sequences of Nuclear Small Subunit Ribosomal RNAs.
Seon Young KIM ; Hack Sung JUNG
Mycobiology 2001;29(2):73-79
The Polyporaceae is a chaotic mass of genera having poroid hymenophores in the Aphyllophorales. To classify the Polyporaceae into more natural groups, phylogenetic analyses were performed using nuclear small subunit ribosomal DNA sequences. Thirty-six species from the families of the Polyporaceae, the Hymenochaetaceae, the Ganodermataceae, the Corticiaceae, the Bondarzewiaceae, the Meruliaceae, the Steccherinaceae and the Lentinaceae were phylogenetically compared. By performing maximum parsimony analysis, seven phylogenetically meaningful groups were identified and discussed. The hyphal system, presence or absence of clamps, and the type of rot were found as important characters in defining the groups. Each group was phylogenetically significant enough to be a core member of each family when the Polyporaceae was split into smaller and more natural families.
DNA, Ribosomal
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Humans
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Phylogeny
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Polyporaceae*
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Polyporales
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RNA, Ribosomal*
4.Molecular Characterization of Fusarium solani and its Formae Speciales Based on Sequences Analysis of the Internal Transcribed Spacer (ITS) Region of Ribosomal DNA.
Young Mi LEE ; Yong Keel CHOI ; Byung Re MIN
Mycobiology 2000;28(2):82-88
The sequences of the internal transcribed spacer (ITS) and 5.8s ribosomal RNA gene (rDNA) from Fusarium solani and its four formae speciales belonging to section Martiella was determined to investigate intraspecific divergence of the ITS regions. The length of the 5.8S, a coding region, was equally 158 bp at all isolates, whereas the variable range of ITS region was shown at 147~152 bp (ITS1) and 148~174 bp (ITS2). According to the maximum-matching method, the matching percentage was 94~100 at 5.8s rDNA, 77~97 at ITS1, and 67~97 at ITS2, respectively. In dendrogram based on the alignment of the ITS sequence data, F.solani f. sp. piperis was distinguished from other isolates belonging to the same species and nucleotide identity was considerably low (41.5%).
Clinical Coding
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DNA, Ribosomal*
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Fusarium*
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RNA, Ribosomal, 5.8S
5.Intrageneric Relationships of Trichoderma Based on Internal Transcribed Spacers and 5.8S rDNA Nucleotide Sequences.
Gi Young KIM ; Goang Jae LEE ; Myung Gyu HA ; Tae Ho LEE ; Jae Dong LEE
Mycobiology 2000;28(1):11-16
The nucleotide sequences of the internal transcribed spacer (ITS) regions of the ribosomal DNA including the 5.8S ribosomal RNA gene (rDNA) have been determined for 11 species in order to analyze their intrageneric relationships. The total length of these sequences ranged from 530 nucleotides for Trichoderma reesei KCTC 1286 to 553 nucleotide for Trichoderma koningii IAM 12534. Generally speaking, the length of ITS1 region was about 30 nucleotides longer than that of the ITS2 region. Also, the sequences of 5.8S rDNA were more conserved in length and variation than those of ITS regions. Although the variable ITS sequences were often ambiguously aligned, the conserved sites were also found. Thus, a neighbor-joining tree was constructed using the full sequence data of the ITS regions and the 5.8S rDNA. The Trichoderma genus used to be grouped on the basis of the morphological features and especially the shape of phialides needs to be reexamined. The phylogenetic tree displayed the presence of monophylogeny in the species of Trichoderma. Therefore, it was difficult to distinguish the intrageneric relationships in the Trichoderma genus.
Base Sequence*
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DNA, Ribosomal*
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Nucleotides
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Phylogeny
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RNA, Ribosomal, 5.8S
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Trichoderma*
6.rDNA ITS sequence analysis of wild Gentiana from Gansu province.
Lisha LIU ; Xiangmei WANG ; Xin WANG ; Lan WANG
China Journal of Chinese Materia Medica 2010;35(5):565-568
OBJECTIVETo find the patterns of the rDNA ITS sequence variation in Gentiana, and establish the molecular biological method for the identification of the four kinds wild Gentiana from different regions in Gansu.
METHODThe ITS gene fragments were PCR amplified and sequenced. The rDNA ITS regions were analyzed by means of the software of Clustal X, MEGA3.
RESULTThe Complete ITS sequence of G. macrophylla, G. straminea, G. dahurica and G. officinale was 800 bp. The sequences of ITS1, ITS2 and 5.8S were 290, 340, 170 bp, respectively. Phylogenetic tree based on ITS1 and ITS2 sequences data was constrcuted by Neighbor-joining method.
CONCLUSIONITS sequence could be as the evidence for the molecular authentication of Gentiana.
DNA, Plant ; chemistry ; DNA, Ribosomal ; chemistry ; DNA, Ribosomal Spacer ; chemistry ; Gentiana ; genetics ; Phylogeny
7.First Report of Stem Rot on Asiatic Dayflower (Commelina communis L.) Caused by Sclerotium rolfsii in Korea.
Okhee CHOI ; Jin Hyeuk KWON ; Yongsik MIN ; Jinwoo KIM
Mycobiology 2011;39(1):57-58
Stem rot was found for the first time on the Asiatic dayflower plant (Commelina communis L.) in Korea. A detailed description of this Korean specimen is given, along with its rDNA internal transcribed spacer sequence. The fungus was identified as Sclerotium rolfsii Saccardo based on mycological characteristics and molecular data.
Commelina
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DNA, Ribosomal
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Fungi
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Korea
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Plants
8.First Report of Botrytis cinerea as a Postharvest Pathogen of Blueberry in Korea.
Jin Hyeuk KWON ; Mi Geon CHEON ; Okhee CHOI ; Jinwoo KIM
Mycobiology 2011;39(1):52-53
Gray mold of blueberry caused by Botrytis sp. is reported for the first time in Korea. A detailed description of the fungus is given, along with its rDNA internal transcribed spacer sequence. The fungus was identified as Botrytis cinerea based on mycological characteristics and molecular data.
Blueberry Plant
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Botrytis
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DNA, Ribosomal
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Fungi
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Korea
9.PCR-Based Sensitive Detection of Wood-Decaying Fungus Phellinus linteus by Specific Primer from rDNA ITS Regions.
Dong Suk PARK ; Hee Wan KANG ; Ki Tae KIM ; Soo Muk CHO ; Young Jin PARK ; Hye Sun SHIN ; Byoung Moo LEE ; Seung Joo GO
Mycobiology 2001;29(1):7-10
Based on the rDNA ITS sequences data, specific primer set for PCR detection of wood-decaying fungus Phellinus linteus was designed. The length of PCR products using designed primer set(SHF and SHR) was about 540 bp. Among 11 species, 17 isolates of Phellinus spp. including Phellinus linteus, P. pomaceus, P. spiculosus, P. baumi, P. pini, P. igniarius, P. gilvus, P. biscuspidatus, P. weirii, P. johnsonianus, P. robutus, and P. igniarius, seven isolates of Phellinus linteus showed about 540 bp-sized single band. This molecular technique could offer a useful tool for detecting and identifying Phellinus linteus.
DNA, Ribosomal*
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Fungi*
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Polymerase Chain Reaction
10.First Report of Rhizopus oryzae as a Postharvest Pathogen of Apple in Korea.
Jin Hyeuk KWON ; Jinwoo KIM ; Won Il KIM
Mycobiology 2011;39(2):140-142
Soft rot in apple caused by Rhizopus oryzae was found for the first time in Korea. A detailed description of the specimen is given along with its internal transcribed spacer rDNA sequence. The fungus was identified as Rhizopus oryzae based on the mycological characteristics, molecular data, and pathogenicity testing.
DNA, Ribosomal
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Fungi
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Korea
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Oryza
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Rhizopus