• Current Research on Agriculture and Life Sciences
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• 제14권
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• pp.101-110
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• 1996

Jar fermentor 배양에서 S. chibaensis J-59로 부터 포도당 이성화효소의 최적 생산조건을 확립하기 위하여 반응표면분석을 이용하였다. 실험계획은 중심계획합성법을 이용하였고, 3가지 실험요인으로는 공기주입량(vvm), 교반속도(rpm), 포도당의 농도(%)로 선별하였다. 요인실험의 결과로 회귀계수를 산출한 후 반응표면 회귀식을 구하였다. 효소 생산량의 변화에 대한 회귀식의 결정계수(R2)는 0.9776이였고, 분산분석의 F-ratio가 12.487이었으며, 이때 유의성(Prob>F)은 5% 이내로 인정되었다. 능선분석 결과, 효소생산 최대값은 공기주입량 2.227vvm, 교반속도 587.5rpm, glucose 농도 0.586%로 나타났으며 이때 반응표면 회귀식에 의해 추정하는 예상 효소활성은 7.67 단위로 나타났다. Jar fermentor 배양에서의 최적화 회귀식에 따라 1% birchwood xylan, 1.5% CSL, 0.1% $MgSO_4{\cdot}7H_2O$, 0.012% $CoCl_2{\cdot}6H_2O$, (pH 7.0)로 구성된 배지에 초기 pH를 7.0으로 조정하여 배양 종료까지 7.0을 유지하면서 공기주입량을 2.2vvm, 교반속도를 580rpm, glucose 농도를 0.586%로 하여 $30^{\circ}C$에서 42 시간 배양하였을때, 실제 효소생산량은 7.43 단위로 상기 분석법에서 예상한 효소 생산량의 97%에 달하였고, 플라스크배양의 효소생산량 (2.78 GIU/ml)보다 약 2.7배 가량 효소생산이 증가되었다.

• 한국응용과학기술학회지
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• 제36권3호
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• pp.748-757
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• 2019

본 연구는 계란 생산성, 계란품질 및 악취저감에 관한 Bacillus subtillus, Streptomyces galilaeus 및 Sphingobacteriaceae로 구성된 복합생균제(PM, probiotic mixture)의 효과를 조사하였다. 산란계 Hy-Line Brown 240수를 4처리구로 구분하여 6주 동안 사육하였다. 처리구는 복합생균제를 함유하지 않은 대조구(CON, control), 일반생균제(CP3, commercial probiotics 0.3%), 복합생균제 3(PM3, 복합생균제 0.3%), 복합생균제 5(PM5, 복합생균제 0.5%)로 구분하였다. 산란율, 계란 호우유니트, 난각두께, 난각강도, 난황색 및 농후난백 높이는 PM3, PM5가 CON 및 CP3에 비해서 높았다. 계분으로부터 암모니아, E. coli, 총호기성균, Coliform, Salmonella 균수는 CON>CP3>PM3>PM5 순서로 증가하였다. 본 결과는 B. subtillus, S. galilaeus 및 Sphingobacteriaceae로 구성된 복합생균제 0.3%가 산란율, 계란품질 개선 및 분에서 암모니아 발생을 낮추어 양계장 악취저감 효과를 갖는다는 점을 보여준다.

• Journal of Microbiology and Biotechnology
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• 제18권4호
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• pp.658-662
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• 2008

Effects of pH shock on the secretion system of S. coelicolor A3(2) have been investigated at a transcriptional level by using DNA microarrays. Actinorhodin secretion was observed to be highly enhanced when an acidic-pH shock was applied to surface grown cultures of S. coelicolor A3(2). In this culture, a gene of actVA-orf1 encoding a putative efflux pump or transporter protein for actinorhodin was strongly upregulated. A major number of efflux pumps for other metabolites and a major number of secretion proteins for protein secretion were also observed to be upregulated with pH shock. The secretion of actinorhodin was observed to be remarkably enhanced in liquid culture as well.

• Applied Biological Chemistry
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• 제35권3호
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• pp.191-195
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• 1992

강낭콩 잎에서 에틸랜에 의하여 유도되는 분자량 30KD인 염기성 키틴분해효소를 정제하고 그 항균활성을 연구하였다. 이 단백질은 chitinase 활성과 lysozyme 활성을 가졌으며, Aspergillus fumigatus, Botrytis cinerea, Fusarium oxysporum, Rhizoctonia solani의 균사 생장을 억제하였다. 그러나 함께 실험한 2종류의 미생물 chitinase, 달걀 lysozyme, 파파야 protease는 이들에 대한 항균작용을 갖지 않았다. 이상의 결과는 lysozyme 활성을 가진 식물 chitinase가 병원균의 균사생장을 억제하여 자신을 방어할 수 있음을 시사한다.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2003년도 생물공학의 동향(XII)
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• pp.422-427
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• 2003

Streptomyces setonii (ATCC 39116) is a Gram-positive thermophilic soil actinomycetes capable of degrading single aromatic compounds including phenol and benzoate via ortho-cleavage pathway. we isolated approximately 6.3-kb S. setonii DNA fragment containing a thermophilic catechol 1,2-dioxygenase(C12O) gene. Here we further revealed that the 6.3-kb S. setonii DNA fragment was organized into two putative divergently-transcribed clusters with 6 complete and one incomplete open reading frames (ORFs). The first cluster with 3 ORFs showed significant homologies to previously known benA, benB, and benC, implying a part of benzoate catabolic operon. The second cluster revealed an ortho-cleavage catechol catabolic operon with three translationally-coupled ORFs (catR, catB, catA). Each of these individually-cloned ORFs was expressed in E. coli and identified as a distinct protein band with a theoretical molecular weight in SDS-PAGE. The expression of the cloned S. setonii catechol operon was induced in a heterologous S. lividans by specific single aromatic compounds including catechol, phenol, and 4-chlorophenol. The simitar induction pattern was also observed using a luciferase gene-fused reporter system, implying that S. setonii employs an inducer-specific regulatory mechanism for aromatic compound metabolism.

• Journal of Microbiology and Biotechnology
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• 제12권4호
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• pp.706-709
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• 2002

Bacterial bioluminescence has been known to be a highly valuable reporter system for its potential application as an effective and simple environmental monitoring method for toxic compounds. In this short report, we constructed a streptomycetes-Escherichia coli shuttle vector-containing bioluminescence system and evaluated its potential application for toxic compounds monitoring. The luxAB biolurninescence genes from Vibrio harveyi were cloned into a streptornycetes-E. coli shuttle vector (named pESK004) and functionally expressed in Streptomyces lividans. The recombinant S. lividans containing pESK004 exhibited an optimal biolurninescence at the optical density ($OD_{600\;nm}$) of 0.4-0.5 and aldehyde concentration of 0.005%. When the recombinant bioluminescence streptomycetes was exposed to a toxic compound such as heavy metals, chlorinated phenols, or pesticides, the bioluminescence was decreased proportionally to the concentration of toxic compound in the assay mixture. The $EC_{50}$ (effective concentration to decrease 50% of the bioluminescence prior to exposure) values in the recombinant biolurninescence streptomycetes for mercury, 2,4-dichlorophenol, and malathion were measured at 2.2 ppm, 144.0 ppm, and 82.4 ppm, respectively. The degree of sensitivity and specificity pattern toward these toxic compounds characterized in this recombinant bioluminescence streptomycetes were unique when compared with previously reported bacterial bioluminescence systems, and this revealed that a recombinant bioluminescence streptomycetes might provide an alternative or complementary system for potential environmental monitoring.

• 한국잠사곤충학회지
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• 제34권2호
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• pp.1-5
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• 1992

전국에서 수집한 토양시료로부터 약 200 여종의 미생물을 분리해내고 이들 균주의 배양 산물액을 대상으로 chitinase 억제능을 조사하였다. 그 결과 누에의 중장 소화관에서 추출한 chitinase crude enzyme과 시판의 정제된 chitinase에 대하여 공통으로 효소의 활성을 억제하는 2개의 균주 S-11과 S-25를 선발하는데 성공하였다. 이들 균주의 배양 산물액을 토사기의 누에에 주사한 결과 대부분의 누에가 용화탈피에 실패하였다.

• 한국토양비료학회지
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• 제45권4호
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• pp.593-601
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• 2012

Heavy metals and metalloids removal can be considered as one of the most important world challenges because of their toxicity and direct impact on human health. Many processes have been introduced but biological processes of remediation seem to offer the most suitable solution in terms of efficiency and low cost. Actinobacteria constitute one of the major microbial populations in soil, and this can be attributed to their adaptive morphological structure as well as their exceptional metabolic power. Among microbes, actinobacteria are morphologic intermediate between fungi and bacteria. Studies on microbial diversities in metal contaminated lands have shown that actinobacteria may constitute a dominantly active microbiota in addition to ${\alpha}$ Proteobacteria. Furthermore, isolation studies have shown metal removal mechanisms which are reminiscent of notable multiresistant strains, such as Cupriavidus metallidurans. Apart from members of genus Streptomyces, which produce more than 90% of commercialized antibiotics, and the nitrogen fixing Frankia, little attention has been given to other members of this phylum. This is because of difficult culture condition requirements and maintenance. In this review, we focused on specific isolation of actinobacteria and their potential applications in metal bioremediation and plant growth promotion.

• 한국미생물·생명공학회지
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• 제23권1호
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• pp.36-42
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• 1995

Actinomycetes occur in a wide range of environments and many more actinomycetes remain to be detected in the natural environment. In isolation stages, selection of the environment as a source of useful isolates is important. Two hundred and eighteen strains were isolated on Bennet's agar and 346 strains were on humic acid-vitamin agar from five each paddy field, field, forest, grass land, riverside soil samples. These isolates were identified to the genus level based on morphological and physiological characteristics. Among them, 386 strains were Streptomyces, 49 strain were Nocardia, 35 strains were Microbispora and Micromonospora each, 15 strains were Nocardiopsis, 13 strains were Actinomadura, 10 strains were Streptosporangium, and the others were isolated rarely. According to soil type, Nocardia, Micromonospora, Microbispora and Streptosporangium were dominant in paddy field, Microbispora Nocardia, Nocardioides and Micromonospora were dominant in field, Nocardia, Micromonospora, Microbispora and Actinomadura were dominant in grass land, Nocardia, Micromonospora and Microbispora were dominant in forest, Nocardia, Microbispora and Micromonospora were dominant in riverside. Generally, Nocardia, Micromonospora, Microbispora and Actinomadura were isolated in all kinds of soils, Streptosporangium were paddy field, Dactylosporangium were forest, Nocardiopsis were field, forest and riverside.

• Journal of Microbiology and Biotechnology
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• 제14권5호
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• pp.1067-1070
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• 2004

In the course of screening for specific inhibitors against the mycelial form of Candida albicans from natural resources, we have isolated and identified A6792-1 from Streptomyces sp. A6792 by using several chromatographies. By spectral analyses, this compound was determined as 7-oxostaurosporine, having a structure of staurosporine aglycon noiety. 7-Oxostaurosporine exhibited a selective growth inhibitory activity against the mycelial form of Candida spp. up to $100\mu\textrm{g}/disc$ in bioassay. It also exhibited a specific antifungal activity against the mycelial form of Candida spp. including C. krusei, C. albicans, C. tropicalis, and C. lusitaniae with MICs ranging from 3.1 to $25\mu\textrm{g}/ml$ 7-Oxostaurosporine demonstrated no in vivo toxicity in SPF ICR mice. Therefore, this compound may have a considerable potential as an antifungal agent based on the preferential inhibition against growth of the mycelial form of Candida spp., dimorphic fungi.