• 한국미생물·생명공학회지
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• 제20권5호
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• pp.583-587
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• 1992

본 연구는 농용항생제인 kasugamycin의 생산을 위하여 S.kasugaensis의 배양조건 및 배지조성을 고찰하였다. Kasugamycin 발효시 최적 탄소원 및 질소원은 각각 soybean oil과 soybean flour였다. 배지 최적온도는 28'C, 최적 pH는 6.6이었다. 본 배양의 최적 접종 상태는 64-68시간 배양한 전배양액으로 접종하였으며, 발효중 물의 첨가는 생산성의 증가를 나타냈으나 소포제로서 silicone coil 첨가는 별 영향을 관찰할 수가 없었다.

• Journal of Microbiology and Biotechnology
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• 제14권1호
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• pp.212-215
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• 2004

In order to develop a biocontrol agent that can effectively control Fusarium wilt on Cymbidium genus, the effectiveness of antagonistic microbes against the cause pathogen was screened. The selected microbe showed a broad spectrum of antifungal activity, and the culture broth of this microbe had better preventive effect on Fusarium wilt than the commercial chemical agent in the pot assay. This isolated strain, GBA-12, was identified as Streptomyces kasugaensis, and the antifungal substance was purified from a broth culture of GBA-12. This purified substance was identified as a polyene macrolide (YS-822A) that was newly discovered from Streptomyces kasugaensis, and it exhibited antifungal activity against several phytopathogenic fungi.

• 한국미생물·생명공학회지
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• 제17권2호
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• pp.131-135
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• 1989

Effects of the inoculum size of testing organism and pH of the plate and the concentration of agar were investigated for the selection of high kasugamycin producing mutants of Streptomyces kasugaensis ATCC 15114. For the detection of high kasugamycin-producing mutants, both concentrations of agar and test organism were optimized at the concentrations of 2% and 0.35 (A$_{550}$), respectively. The pH 7 was optimum for both growing the testing organism, Pseudomonas fluorescens IFO 12180, and for obtaining more promising mutant strains of S. kasugaensis. Under these conditions, mutants had been isolated which, tested later in liquid cultures, gave higher kasugamycin yields than that of the parent strain.

• 한국식물병리학회:학술대회논문집
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• 한국식물병리학회 2002년도 총회 및 추계학술발표회
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• pp.56.1-56
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• 2002

• 환경위생공학
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• 제23권4호
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• pp.23-29
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• 2008

This study was performed to develop mutant strain using a combination of UV irradiation procedures with protoplast mutagenesis in order to achieve an effective kasugamycin production from Streptomyceskasugaensis. Whenlessthan 1.0g/lof Linoleic acid was used, the cell growth was not inhibited. On the other hand, the cell growth was greatly inhibited when more than 1.6 g/l of linoleic acid was used. Among the various mutant strains, SK-12 was obtained in medium containing 1.6g/l of linoleic acid, showing the highest rate of both cell growth and kasugamycin production. In order to compare kasugamycin production with the SK-12 and the parent strain using soybean oil, cultures were performed in a flask. The production of kasugamycin was increased with the increase time. The maximum kasugamycin concentration was 1.2g/l after 6 days of culture. The product yield from soybean oil was 0.05g/l/g consumed carbon source, which was roughly 5.0 fold higher than the parent strain. These results show that it was effective method for obtaining a mutant resistant to linoleic acid for the effective production of kasugamycin from soybean oil.

• Journal of Microbiology and Biotechnology
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• 제15권3호
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• pp.491-496
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• 2005

The biosynthetic gene cluster for the aminoglycoside antibiotic kasugamycin was isolated and characterized from the kasugamycin producing strain, Streptomyces kasugaensis KACC 20262. By screening a fosmid library using kasA, the gene encoding aminotransferase, we isolated a 22 kb DNA fragment. The fragment contained seventeen complete open reading frames (ORFs); one of these ORFs, kasD, was identified as the gene for dNDP-glucose 4,6-dehydratase, which catalyzes the conversion of dNDP-glucose to 4-keto-6-deoxy-dNDP-glucose. The enzyme showed a broad spectrum of substrate specificity. In addition, ksR was overexpressed in E. coli BL21 and proved to be a self-resistance gene against kasugamycin. These findings suggest that the isolated gene cluster is highly likely responsible for the biosynthesis of kasugamycin.

• 청정기술
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• 제4권1호
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• pp.45-59
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• 1998

방선균인 Streptomyces kasugaensis에 의해서 생산되는 이차대사산물인 kasugamycin 생산성 증대 및 단위 생산량 당 오염물질 배출량 저감을 위한 연속 고정화 배양을 수행하였다. 세포 고정화에 적합한 포자 수확을 위한 포자형성 촉진 배지 개발은 물론 고정화 담체로 사용한 셀라이트에 수확된 포자를 고정화시키는 방법을 확립하였다. 연속 고정화 배양 시 고정화세포의 유출을 방지함으로써 안정된 연속배양을 가능토록 하기위한 decantor 형태의 고정화세포 분리기가 장착된 반응기를 사용하였다. 희석 속도 및 공급액 중의 기질 농도(당 농도, 인 농도)를 변화시키며 생합성된 kasugamycin 생산성 및 화학적산소요구량(COD)을 측정하였으며 이들을 현탁세포를 이용한 회분식 발효에서의 kasugamycin 생산성 및 발효 폐액 중의 COD 값과 비교하였다. 고정화 세포를 이용한 연속배양에서의 kasugamycin 생산성이 현탁세포를 이용한 회분식 발효에 비해 2.5배 높았으며, 동시에 단위 생산량 당 COD가 2.3배 저감되는 것으로 나타났다. 이것으로부터 연속 고정화 배양이 현탁 회분식 배양에 비해 kasugamycin 생산성 및 오염물질 배출 측면에서 유리한 청정 공정임을 확인할 수 있었다.