• 한국응용곤충학회지
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• 제47권2호
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• pp.175-184
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• 2008

국내의 난방제 해충에 선택적으로 생물활성을 나타내는 균주를 선발하기 위하여 작물재배 지역의 토양으로부터 채취한 115개의 토양샘플 중 46개의 Bacillus thuringiensis 균주를 분리하였다. 이러한 B. thuringiensis균주를 사용하여 난방제 농업해충에 생물활성을 검정한 결과 배추좀나방(Plutella xylostella)에 CAB119을 포함한 35균주, 파밤나방(Spodoptera litura)에는 CAB128, CAB141균주가, 담배거세미나방(Spodoptera exigua)은 CAB133과 CAB159균주가 효과를 나타냈으며 CAB162균주는 3종류의 모든 해충에 높은 활성을 보였다. 분리된 B. thuringiensis CAB133 균주는 H serotype에 의한 혈청학적 동정과 SDS-PAGE를 통한 독소 단백질 패턴에서 B. thuringiensis subsp. kurstaki (3abc)로 동정되었다. 담배거세미나방 2령 유충에 대한 활성검정의 결과 B. thuringiensis subsp. kurstaki (3abc) CAB133, CAB162의 두 균주에 대한 $LD_{50}$ 값은 각각 0.089, $3.144{\mu}g/ml$로 높은 활성을 나타났다. 담배거세미나방의 령기에 따른 생물실험에서 CAB133 균주 $1.5{\times}10^6(cfu/ml)$에서 1령의 경우 3일, 2령은 5일에 100%의 사충율을 보였다. 담배거세미나방의 경우 B. thuringiensis를 섭식 후 먹기를 중단하여 성장이 멈추면서 $5{\times}7$일 후에 사망하였다. 그러므로 B. thuringiensis의 결정성독소단백질$(1.267{\mu}g/ml)$를 섭식하고 성장하지 못하는 담배거세미나방 유충의 무게는 대조군보다 5일후 약 30배정도 차이로 나타나서 사망하였다.

• 한국미생물·생명공학회지
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• 제19권3호
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• pp.303-307
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• 1991

B.thuringiensis subsp. darmstadiensis 73E10-2의 내독소에 존재하는 hemolysin이 Sephadex G-100 gel filtration과 DEAE-cellulose ion exchange column chromatography에 의해 정제되었으며, 그 순도는 SDS-PAGE와 Ouchterlony test로 확인하였다. 그 결과 정제된 hemolysin의 분자량은 64KDa 의 단백질 이었으며, in vivo 상태에서는 전혀 모기유충에 독작용을 나타내지 않았다는 점이 28KDa 단백질의 차이가 있었다. 또한 정제된 hemolysin과 B.thuringiensis subsp. israelensis의 내독소를 효소항체법으로 검토해 본 결과 양단백질 사이에는 면역학적으로 전혀 상관이 없었다.

• 한국미생물·생명공학회지
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• 제14권4호
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• pp.325-328
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• 1986

The lethality to Pieris raepi larvae and the safety tests to mice of the endotoxin crystals and the pesticide of B thuringiensis serovar kurstaki were carried out. The LD50 of the endotoxin (3.9$\times$10$^9$ spores/$m{\ell}$) appeared to be 1$\mu$g and that of the pesticide (2.6$\times$10$^9$ spores/$m{\ell}$) was about 9 $\mu$g. When the endotoxin solution and the pesticide were injected to the mice's intraperitoneal cavities, 10 to 20% of the mite were dead. Also in the case of intracerebral injection 20% of the mice were dead at the doses of 7.8$\times$10$^3$ spores and 100% of the mice were dead at the concentration of 7.8$\times$10$^8$ spores. but the mice in the oral, subcutaneous and inhalation treatment groups were safe and healthy. When the pesticide applied to the cabbage field for raepi larvae, 52 to 65% of the larvae in the field were killed in 4 days postapplication.

• International Journal of Industrial Entomology and Biomaterials
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• 제9권2호
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• pp.183-186
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• 2004

Recently, we have developed an easy, simple and convenient circular DNA cloning system named plasmid capture system (PCS). To investigate usefulness of PCS in cloning of plasmids from Bacillus thuringiensis strains, PCS donors, pPCS-S and pPCS-L were applied to clone plasmids of B. thuringiensis subsp. israelensis by in vitro transposition using 4{TnsABC^*}$ transposase. In result, 3 small plasmids were cloned, and these were consistent with pTX14-1, pTX14-2 and pTX14-3 reported previously from B. thuringiensis subsp. israelensis. Therefore, the PCS can be successfully applied to clone small plasmids from B. thuringiensis strains.

• 생명과학회지
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• 제6권4호
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• pp.293-298
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• 1996

Thirteen subspecies of Bacillus thuringiensis including B. t. israelensis, B. t. morrisoni PG-14 and B.t. darmstadoemsos known to be toxic to dipteran insects were treated on the mushroom (Flammulina velutipes) compost to estimate the biological control effect of a sciarid fly, Lycoriella sp. According to the results, it was found that there were no significant effects of the tested strains of B, thuringiensis on the control of Lycoriella sp. For further confirmation, larval gut juice of Lycoriella sp. and trypsin were respectively treated into the parasporal crystal proteins of three subspecies of B. t. israelensis, B. t. morrisoni PG-14, and B. t. darmstadiensis. The proteins were separated by SDS-PAGE. According to the results, the major parasporal crystal proteins were respectively produced by B. t. morrisoni as the amount of 52 kd, B. y. israelensis as 37kd and B. t. darmstadiensis as 39kd, but the activity of these proteins could not be unfortunately confirmed in this study.

• Journal of Microbiology and Biotechnology
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• 제16권11호
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• pp.1713-1719
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• 2006

A method for the simple, rapid, specific, and accurate detection of Bacillus anthracis spores was developed by employing specific capture peptides conjugated with fluorescent quantum dots (QDs). It was possible to distinguish B. anthracis spores from the spores of B. thuringiensis and B. cereus using these peptide-QD conjugates by flow cytometric and confocal laser scanning microscopic analyses. For more convenient high-throughput detection of B. anthracis spores, spectrofluorometric analysis of spore-peptide-QD conjugates was performed. B. anthracis spores could be detected in less than 1 h using this method. In order to avoid any minor yet false-positive signal caused by the presence of B. thuringiensis spores, the B-Negative peptide, which can only bind to B. thuringiensis, conjugated with another type of QD that fluoresces at different wavelength was also developed. In the presence of mixed B. anthracis and B. thuringiensis spores, the BABA peptide conjugated with QD525 and the B-Negative peptide conjugated with QD585 were able to bind to the former and the latter, specifically and respectively, thus allowing the clear detection of B. anthracis spores against B. thuringiensis spores by using two QD-labeling systems. This capture peptide-conjugated QD system should be useful for the detection of B. anthracis spores.

• International Journal of Industrial Entomology and Biomaterials
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• 제8권1호
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• pp.61-66
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• 2004

Bacillus thuringiensis 656-3 which was isolated from a soil sample of mushroom house and showed high toxicity to mushroom flies, Lycoliella mali and Coboldia fuscipes, was surveyed for insecticidal effect in the oyster mushroom house.3. thutingiensis 656-3 was mass-cultured in the fermenter containing soybean cake(2%) and wheat bran (2%) as media source. Semi-for-mutation of B. thuringiensis 656-3 was performed with metamorphic starch only. When the formulation suspension containing $5{\times}{10^7}$ cfu was sprayed on the mushroom in mushroom house, the insecticidal effect of B. thuringiensis 656-3 to mushroom flies,1. mali and C. fuscipes, was maintained over 90% by the fifth day after starting spraying. The yield of oyster mushroom house with B. thuringiensis 656-3 was significantly increased compared to control. B. thuringiensis 656-3 represents a powerful biological insecticide for the control of mushroom flies.

• 환경위생공학
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• 제12권2호
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• pp.59-64
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• 1997

For purification of a 70kDa toxic protein of mosquitocidal delta-endotoxin from B. thuringiensis strain H9B, immuno-affinity chromatography was performed. After separation of 70kDa toxic proteins from the delta-endotoxin of the strain H9B on SDS-PAGE, the 70kDa toxic protein was subcutaneously injected into rabbit for making a polyclonal antibody. A anti-70kDa toxic protein was purified by a column chromatography packed with protein A-sepharose 4B gels. The 70kDa toxic protein from delta-endotoxin of the strain H9B was also purified by an immuno-affinity chromatography packed with CNBr-activated sepharose 4B gels conjugated anti-70kDa toxic protein after elution with 1/10M citric acid-1/5M Na$_{2}$HPO$_{4}$ buffer(pH3.2) containing 0.5M NaCl. The 70kDa toxic protein was purified through only one step-separation system, was demonstrated by SDS-PAGE and immunoblot.

• 한국응용곤충학회지
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• 제48권4호
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• pp.509-517
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• 2009

국내에서 분리된 Bacillus thuringiensis subsp. aizawai CAB109균주가 난방제 해충으로 알려진 담배거세미나방과 파밤나방에 동시에 높은 독성을 보이는 것으로 나타났다. B.t. CAB109 균주의 활성을 평가하기 위해 혈청형이 aizawai이면서 미생물농약으로 시판중인 TB-WP제품 및 SC제품과의 살충활성을 비교한 결과, B.t. CAB109균주, TB-WP제품, SC제품은 담배거세미나방 2령충에 대한 반수치사농도($LC_{50}$)가 각각 $1.3{\times}10^5cfu/ml$, $2.3{\times}10^6cfu/ml$, $5.2{\times}10^5cfu/ml$으로 나타났고 파밤나방 2령충에 대한 반수치사농도는 $1.8{\times}10^4cfu/ml$, $1.3{\times}10^6cfu/ml$, $1.5{\times}10^6cfu/ml$으로 나타나 두 종 해충 모두에서 B.t. CAB109 균주가 독성이 더 높은 것을 볼 수 있었다. B.t. CAB109균주가 이미 알려져 있는 aizawai와 비교해 차이가 나는 새로운 유전자를 소유하는지 확인하기 위해 Plasmid DNA를 추출하여 전기영동 한 결과 B.t. subsp. aizawai HD-133과 다른 패턴을 보이는 것을 확인 할 수 있었고 Cry1-Cry5의 primer를 사용하여 PCR을 진행한 결과 B.t. subsp. aizawai CAB109균주는 Cry1Aa, 1Ab, 1C, 1D를 B.t. subsp. aizawai HD-133은 Cry1Aa, 1Ab를 가지고 있음을 확인 할 수 있었다.

• 한국미생물·생명공학회지
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• 제27권5호
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• pp.359-363
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• 1999

To prevent appearance of resistant mosquitoes against $\delta$-endotoxin of bacillus thuringiensis subsp. israelensis (Bti) in field, a mosquitocidal Bacillus thuringiensis strain 21-2(Bt21-2) producing a new type of $\delta$-endotoxin was isolated. The strain Bt 21-2 belongs to H serotype 43, B. thuringiensis subsp. guiyangiensis (Btg). The $\delta$-endotoxins from the strain Bt 21-2 and the strain Bti were a cuboid shape morphologically, but the $\delta$-endotoxin of the strain Bt 21-2 was composed of 150, 90 and 70kDa proteins on SDS-PAGE, and the antigenicity of $\delta$-endotoxin of the strain Bt 21-2 was different from that of the strain Bti on immunoblot. The $\delta$-endotoxin gene of the strain Bt 21-2 was not amplified with specific primers of $\delta$-endotoxin gene (cry4A and cry4B) of the strain Bti on PCR.