• The Korean Journal of Mycology
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• v.23 no.4 s.75
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• pp.318-324
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• 1995

The evolutionary relationships of the genus Trichoderma and related taxa were assessed using partial sequencing of 18S ribosomal RNA. Phylogenetic tree divided into three major groups; 1. Saccharomyces cerevisiae-Geotrichum klebahnii-Alternaria mali group; 2. Neurospora crassa-Aspergillus-Penicillium-Chrysosporium pannorum-Scopulariopsis sp. group; 3. Trichoderma group. The genus Trichoderma seemed to be phylogenetically separated from Saccharomyces cerevisiae, Aspergillus and Penicillium groups, and have passed through it's own evolutionary pathway.

• Archives of Pharmacal Research
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• v.8 no.3
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• pp.149-157
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• 1985

The HCL hydrolyzate of the non-histone protein fractionated from the rat liver nuclei which have been incubated inthe presence of S-adenosyl-L-[methyl-$^{14}C$ ]-methionine shows at least four unidentified radioactive peaks on a basic amino acid analysis chromatogram. One of these unknown compounds (designated as compound 3) is also formed by the rat liver homogenated with the exogenous addition of an appropriate protein substrate. Since boiled rat liver homogenate or fresh homogenate in the absence of an exogenous protein substrate failed to form compound 3, its formation can be considered to be enzyme-catalyzed. The enzyme which yields compound 3 shows a preference of protein substrate in the order of reductively methylated hemoglobin > native > histone type II-A. The rat enzyme is nuclear in location associated with chromatin, and exhibits the highest activity in the liver among various rat organs. A compound 3-forming enzyme is also present in Neurospora crassa, since endogenous formation of the compound 3 can be demonstrated with the crude extract of this mold. The chemical identity of compound 3 is not yet known. However, it resisted to the following treatments; 6 N HCL and 0.1 N Na NaOH hydrolysis at $110^{\circ}C$, OR L-amino acid oxidase.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.10 no.6
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• pp.1287-1291
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• 2009

The genes of cyanide hydratase(CHT), a kind of nitrilases whichhydrolyze cyanide to formamide were extracted from N. crassa and A. nidulans, the two fungal strains. The recombinant forms of the CHT originated from N. crassa and A. nidulans were prepared with N-terminal hexahistidine purificationtags or no tags, and expressed in E. coli. The enzymes were purified using immobilized metal affinity chromatography. They were compared according to their pH activity profiles, and kinetic parameters. The N. crassa CHT has the wider pH range of activity above 50% and three-fold higher turnover rate (6.6 ${\times}$ $10^8$ $min^{-1}$) than the A. nidulans, meanwhile the CHT of A. nidulans has the higher $K_m$ value. Expression of CHT in both N. crassa and A. nidulans were induced by the presence of KCN, regardless of any presence of nitrogen sources. Max. 82% of KCN was degraded in 60 min for biological degradation tests.

• Journal of Environmental Science International
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• v.17 no.11
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• pp.1221-1226
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• 2008

A variety of fungal species are known to degrade cyanide through the action of cyanide hydratase, a specialized nitrilases which hydrolyze cyanide to formamide. This work is a report on two unknown and un-characterized members from Neurospora crassa and Aspergillus nidulans. Recombinant forms of three cyanide hydratases (CHT) originated from N. crassa, Gibberella zeae, and A. nidulans were prepared after their genes were cloned with N-terminal hexahistidine purification tags, expressed in E. coli and purified using immobilized metal affinity chromatography. These enzymes were compared according to their pH activity profiles, and kinetic parameters. Although all three were similar, the N. crassa CHT has the widest pH range of activity above 50% and highest turnover rate ($6.6{\times}10^8min^{-1}$) among them. The CHT of A. nidulans has the highest Km value of the three nitrilases evaluated in here. Expression of CHT in both N. crassa and A. nidulans were induced by the presence of KCN, regardless of any presence of nitrogen sources. These data can be used to determine optimal procedures for the enzyme uses in the remediation of cyanide-containing wastes.

• The Microorganisms and Industry
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• v.19 no.1
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• pp.2-7
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• 1993

polyamine을 생합성하는 율속단계효소인 ornithine decarboxylase(ODC)는 미생물에서 많이 연구되어 왔으며 실제적으로 이 효소에 대한 연구는 세균에서 그 효시를 이루었다(1-5,19,35). 최근 들어서는 Escherichia coli(1-22), Saccharomyces cerevisiae (35-40), Neurospora crassa, Physarum polycephalum에서 보다 상세한 연구가 이루어졌는데, 본 고에서는 Escherichia coli, Saccharomyces cerveisiae에 관하여 좀 더 자세히 살펴보고자 한다. Polyamines의 연구나 ODC효소에 대한 연구는 미생물이 많이 이용되었는데, 이는 비교적 쉽게 세포배양이 되기도 하지만, ODC가 결손된 변이주를 만들기가 비교적 용이한 이유도 있었다.

• The Plant Pathology Journal
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• v.29 no.3
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• pp.234-241
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• 2013

Polygalacturonase (PG) gene is a typical gene family present in eukaryotes. Forty-nine PGs were mined from the genomes of Neurospora crassa and five Aspergillus species. The PGs were classified into 3 clades such as clade 1 for rhamno-PGs, clade 2 for exo-PGs and clade 3 for exo- and endo-PGs, which were further grouped into 13 sub-clades based on the polypeptide sequence similarity. In gene structure analysis, a total of 124 introns were present in 44 genes and five genes lacked introns to give an average of 2.5 introns per gene. Intron phase distribution was 64.5% for phase 0, 21.8% for phase 1, and 13.7% for phase 2, respectively. The introns varied in their sequences and their lengths ranged from 20 bp to 424 bp with an average of 65.9 bp, which is approximately half the size of introns in other fungal genes. There were 29 homologous intron blocks and 26 of those were sub-clade specific. Intron losses were counted in 18 introns in which no obvious phase preference for intron loss was observed. Eighteen introns were placed at novel positions, which is considerably higher than those of plant PGs. In an evolutionary sense both intron loss and gain must have taken place for shaping the current PGs in these fungi. Together with the small intron size, low conservation of homologous intron blocks and higher number of novel introns, PGs of fungal species seem to have recently undergone highly dynamic evolution.

• Proceedings of the Korean Vacuum Society Conference
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• 2013.02a
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• pp.519-519
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• 2013

본 연구에서는, 전기적 충격이 없고 넓은 면적을 동시에 처리할 수 있는 형태의 유전체 장벽 방전(DBD: Dielectric Barrier Discharge)을 이용한 대기압 저온 플라즈마 장치를 제작하고 이를 이용하여 빵 곰팡이(Neurospora crassa) 살균에 대한 기본 분석을 하였다. 실험에 사용한 저온 대기압 면방전 플라즈마의 파워는 사인파 교류전압을 인가하여, 방전전압은 1.4~2.3 kV, 방전전류는 20~30 mA의 값을 가지며, 전압과 전류의 위상차는 약 80도의 기울기 차이가 난다. 이때의 출력은 약 4 W를 가지며, 공랭식 쿨러를 이용하여 유전체의 열을 배출하였다. 시료대의 온도 측정결과 방전과 동시에 쿨러를 작동할 경우 최대 10분에서 37도를 넘지 않았다. 장치에서 발생하는 플라즈마에 의한 O3의 양은 플라즈마 발생부로부터 10 mm 이내에서 약 25~30 ppm 이 측정되었으며, NO나 NO2 는 거의 검지되지 않았다. 증류수(Deionized water)속에 담긴 빵 곰팡이(Neurospora crassa) 포자를 면방전 플라즈마 발생장치로 처리하였을 때, 포자의 발아율은 처리시간 및 출력파워가 증가함에 따라 급격히 감소하였으나 VM (Vogel's Minimal) 배양액에 넣고 플라즈마 처리를 한 경우에는, 증류수의 결과와 달리 살균효과가 미비함을 보였다. MTT 측정법 또한 같은 경향성을 보였으며, 이를 통해 포자를 둘러싸고 있는 환경이 플라즈마의 살균효과에 영향을 미치는 것으로 보인다. 본 실험을 통해, 유전체 장벽을 이용한 면방전 플라즈마 발생장치가 플라즈마 제트(jet)와 달리 직접적인 플라즈마 접촉 없이도 미생물 살균이 가능하다는 것을 보았으며, 처리대상의 생체용액과 같은 주변 환경에 영향을 받음을 알 수 있었다. 또한 면방전 플라즈마 장치로부터 발생하는 O3과 같은 활성종들이 빵 곰팡이의 비활성화에도 역할을 할 수 있음을 알 수 있었다.

• Korean Journal of Microbiology
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• v.35 no.3
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• pp.192-196
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• 1999

CHEF-PFGE(Contour-Clarnped Homogeneous Electric field- Pulsed Field Gel Electrophoresis) was used to identify electrophoretic karyotype for eight strains belonging to the Fzisoriuni section Liseolo. Chromosome numbers were nine to thirteen bands, ranging in size Cram 0.75 to 6.45 Mb. The total genome size was eslimated to range from 38.19 Mb to 43.12 Mb and numerous chromosome-length polymorphisms (CLPs) were observed. For the chromosome localizalion of the gene, 1GS sequence(2.6 Kb) of rDNA from F: moniliforme, chs-2 gene(2.8 Kb) and 4 - 3 gene(3.8 Kb) from Neuuospora cmssa were wed as probes.

• Journal of Conservation Science
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• v.7 no.1
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• pp.31-41
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• 1998

Two isolation methods using the open plate and air sampler were applied to examine microbial distribution as an environmental factor for conservation of cultural properties in the War Memorial in Korea. The numbers of fungi were the abundant in the air of entrance and inside of the exhibition room where visitors were crowded, compared with inside of repository rooms. Fungal and bacterial distributions in the exhibition room during exhibition period were higher than during nonexhibition period, These results are due to the inflow of air current carrying microoganisms to the exibition rooms from outside with visitors. Fungi isolated from the War Memorial were identified as 19 species and one thermophilic fungus, Neurospora crassa. The majority of the isolated fungi are seemed to cause damage to cellulose materials in the Memorial.

• Journal of Microbiology
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• v.44 no.5
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• pp.556-561
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• 2006

A differential display for the expression profiles of wild-type Cryphonectria parasitica and its virally-infected isogenic hypovirulent strain revealed several transcripts of interest, which evidenced significant matches with fungal genes of known function. Among which, we have further analyzed an amplified PCR product with significant sequence similarity to the known fungal stress-responsive thioredoxin gene from Neurospora crassa. The product of the cloned thioredoxin gene, CpTrx1, consists of 117 amino acids, with a predicted molecular mass of 13.0 kDa and a pI of 5.4. Sequence comparisons demonstrated that the deduced protein sequence of the CpTrx1 gene evidenced a high degree of homology to all known thioredoxins, with the highest degree of homology with trx1, a thioredoxin gene from Saccharomyces cerevisiae, and evidenced a preservation of the conserved hall markresidues (Trp-Cys-Gly-Pro-Cys) at the active site of thioredoxin. The E. coli-generated CpTRX1 manifested thioredoxin activity, according to the insulin reduction assay, which indicates that the cloned gene does indeed encode for the C. parasitica thioredoxin.