• 제목/요약/키워드: crystal proteins

검색결과 132건 처리시간 0.028초

Expression and Characterization of Recombinant Cry1Ac Crystal Proteins with Foreign Proteins in Bacillus thuringiensis subsp. kurstaki Cry ̄B

  • Roh, Jong-Yul
    • 한국잠사학회:학술대회논문집
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    • 한국잠사학회 2003년도 제46회 춘계 학술연구 발표회
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    • pp.31-32
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    • 2003
  • Bacillus thuringiensis produces insecticidal parasporal inclusions (crystal protein) used as a major ingredient of most microbial insecticides. Although many B. thuringiensis strains and their crystal proteins have been isolated and characterized, such findings have limitation of usefulness. For enhanced toxicity, fast effects, and the delay of resistance development, research on genetic manipulation of crystal genes and proteins by genetic engineering should be continued. (omitted)

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Expression and Morphology of Crystal Proteins in Bacillus thuringiensis subsp. kurstaki Cry-B

  • Park, Hyeon-U;Kim, Ho-San;Kim, Yeong-Hun;Jin, Byeong-Rae;Gang, Seok-Gwon
    • 한국잠사곤충학회지
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    • 제36권2호
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    • pp.157-161
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    • 1994
  • B. thuringiensis subsp. kurstaki Cry-B에서 cryIA(b) 유전자 promoter 조적을 받는 cryIA(c) 유전자와 그 자신의 promoter 조절을 받는 cryIIA 유전자의 발현 여부와 내독소 단백질의 형태를 관찰하기 위하여, 이들 두 내독소 단백질 유전자를 B.thuringiensis - E. coli shuttle vector를 이용하여 발현벡터 pKC1A와 pKC2A를 각각 제작하였다. 발현벡터 pKC1A와 pKC2A를 B. thuringiensis subsp. kurstaki Cry-B 균주에 형질전환시키고, 이들 형질전환체로부터 각각 bipyramid형과 cuboid형의 정상적인 내독소 단백질이 발현되었음을 확인하였다.

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Developing 500 MHz NB 19F-13C Double Resonance Solid-State NMR Probe for in-situ Analysis of Liquid Crystal Display Panels

  • Choi, Sung-Sub;Jung, Ji-Ho;Park, Yu-Geun;Park, Tae-Joon;Park, Gregory Hyung-Jin;Kim, Yong-Ae
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1577-1580
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    • 2012
  • The orientational and dynamic behavior of liquid crystal molecules on the alignment layer surfaces of liquid crystal display (LCD) devices is crucial to their performance, but there are only a few methods of experimentally elucidating the interactions between the liquid crystals and the alignment layers. Inspired by the natural and technical similarities between membrane proteins in lipid bilayers and liquid crystals in LCDs, we employed solid-state NMR methodologies originally developed for the study of membrane proteins in lipid bilayers for the in-situ analysis of liquid crystal display panels. In this article, we present a home-built 500 MHz narrowbore (NB) The orientational and dynamic behavior of liquid crystal molecules on the alignment layer surfaces of liquid crystal display (LCD) devices is crucial to their performance, but there are only a few methods of experimentally elucidating the interactions between the liquid crystals and the alignment layers. Inspired by the natural and technical similarities between membrane proteins in lipid bilayers and liquid crystals in LCDs, we employed solid-state NMR methodologies originally developed for the study of membrane proteins in lipid bilayers for the in-situ analysis of liquid crystal display panels. In this article, we present a home-built 500 MHz narrowbore (NB) $^{19}F-^{13}C$ double resonance solid-state NMR probe with a flat-square coil and the first application of this probe for the in-situ analysis of LCD panel samples. double resonance solid-state NMR probe with a flat-square coil and the first application of this probe for the in-situ analysis of LCD panel samples.

Biochemical and Structural Analysis of Hormone-sensitive Lipase Homolog EstE7: Insight into the Stabilized Dimerization of HSL-Homolog Proteins

  • Nam, Ki-Hyun;Park, Sung-Ha;Lee, Won-Ho;Hwang, Kwang-Yeon
    • Bulletin of the Korean Chemical Society
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    • 제31권9호
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    • pp.2627-2632
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    • 2010
  • Hormone sensitive lipase (HSL) plays a major role in energy homeostasis and lipid metabolism. Several crystal structures of HSL-homolog proteins have been identified, which has led to a better understanding of its molecular function. HSL-homolog proteins exit as both monomer and dimer, but the biochemical and structural basis for such oligomeric states has not been successfully elucidated. Therefore, we determined the crystal structure of HSL-homolog protein EstE7 from a metagenome library at $2.2\;{\AA}$ resolution and characterized the oligomeric states of EstE7 both structurally and biochemically. EstE7 protein prefers the dimeric state in solution, which is supported by its higher enzymatic activity in the dimeric state. In the crystal form, EstE7 protein shows two-types of dimeric interface. Specifically, dimerization via the external ${beta}8$-strand occurred through tight association between two pseudosymmetric folds via salt bridges, hydrogen bonds and van der Waals interactions. This dimer formation was similar to that of other HSL-homolog protein structures such as AFEST, BEFA, and EstE1. We anticipate that our results will provide insight into the oligomeric state of HSL-homolog proteins.

Bacillus thuringiensis를 이용한 버섯 파리(Lycoriella sp.)의 생물적 방제에 관한 연구 (A stydy on The Biological Control of Sciarid Fly(Lycoriella sp.) Using Bacillus thuringiensis)

  • 최광호;박현철;박현우;진병래;강석권;손흥대
    • 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.

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Isolation and Characterization of Strain of Bacillus thuringiensis subsp. kenyae Containing Two Novel cry1-Type Toxin Genes

  • Choi, Jae-Young;Li, Ming Shun;Shim, Hee-Jin;Roh, Jong-Yul;Woo, Soo-Song;Jin, Byung-Rae;Boo, Kyung-Saeng;Je, Yeon-Ho
    • Journal of Microbiology and Biotechnology
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    • 제17권9호
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    • pp.1498-1503
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    • 2007
  • To identify novel crystal proteins, Bacillus thuringiensis 2385-1 was isolated from Korean soil samples and characterized. The H-serotype of 2385-1 was identical to that of subsp. kenyae (H4a4c), and its crystal toxin was bipyramidal-shaped. However, 2385-1 showed a much higher toxicity towards Plutella xylostella and Spodoptera exigua larvae than subsp. kenyae. In addition, the crystal protein profile and plasmid DNA pattern of 2385-1 differed from those of subsp. kenyae. To verify the crystal protein gene types of 2385-1, a PCR-RFLP analysis was performed, and the results revealed that 2385-1 contained two novel cry1-type crystal protein genes, cryl-5 and cry1-12, in addition to the crylJal gene. The deduced amino acid sequences of cryl-5 and cry1-12 showed a 97.9% and 75.7% sequence similarity with the CrylAb and CrylJa crystal proteins, respectively. Among the novel crystal proteins, Cry1-5 showed a high toxicity towards P. xylostella and S. exigua larvae. In conclusion, B. thuringiensis 2385-1 is a new isolate in terms of its gene types, and should be a promising source for an insecticide to control lepidopteran larvae.

Bacillus thuringiensis 생장과 살충성 결정단백질 생성에 대한 탄소원의 영향 (Growth and Production of Insecticidal Crystal Proteins of Bacillus thuringiensis as Affected by Carbon Sources)

  • 김무기;안병구
    • Applied Biological Chemistry
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    • 제39권3호
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    • pp.177-182
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    • 1996
  • 액체배양 실험으로 14가지 탄수화물을 사용하여 B. thuringiensis의 생장, 포자형성 및 살충성 결정단백질 생성에 대한 탄소원의 영향을 조사하였다. 최대 세포밀도는 B. thuringiensis 균주에 따라 접종 $16.7{\sim}22$시간 후에 모든 탄소원배지에서 $10^7{\sim}10^8\;cells/ml$ 수준으로 나타났고, 접종 $16.7{\sim}24.7$시간 후에 포자가 나타나기 시작하여 포자형성율이 80%에 이르는 시간은 균주에 따라 $28{\sim}51.3$ 시간이 소요되었다. 배양에 따른 배지의 pH변화는 없었고, 단백질 총량은 sucrose를 사용한 배지에서 가장 높았고, 전분을 첨가했을때 가장 낮았다. Glucose, lactose, maltose 또는 sucorse를 탄소원으로 사용한 배지에서 살충성 결정단백질 생성량이 많았고, 단백질 총량과 살충성 결정단백질량은 비례관계에 있었다. B.t. kurstaki와 B.t. israelensis에서 생성되는 서로 다른 종류의 살충성 결정 단백질의 양은 사용한 모든 탄소원의 경우 그 개별적 증감의 경향이 같았다.

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Structural Basis of the Disease-related Proteins: Target Oriented Structural Proteomics

  • Jinho Moon;Heo, Yong-Suk;Kim, Young-Kwan;Kim, Hye-Yeon;Park, Min-Hye;Hwang, Kwang-Yeon
    • 한국결정학회:학술대회논문집
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    • 한국결정학회 2003년도 춘계학술연구발표회
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    • pp.15-15
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    • 2003
  • To discover new drugs more quickly and more efficiently, pharmaceutical companies and biotechnology firms are increasingly turning to the genomics and the structural proteomics technologies. Structural-proteomics can provide a foundation for this through the determination and analysis for protein structure on a genomics scale. Among many structures determined by CGI, we will present with the representative examples drawn from our work on novel structures or complex structures of the disease-related proteins. The alpha subunit of Hypoxia-inducible factor (HIF) is targeted for degradation under normoxic conditions by an ubiquitin-ligase complex that recognizes a hydroxylated proline residue in HIF. Hydroxylation is catalysed by HIF prolyl 4-hydroxylases (HIFPH) which are fe(II) and 2-oxoglutarate (2-OG) dependent oxygenases. Here, we discuss the first crystal structure of the catalytic domain of HIFPH in complexes, with the Fe(II)/2-OG at 1.8Å. These structures suggest that the Ll region (residues 236-253), which is also conserved in mammals, form a 'lid' that closes over the active site. The structural and mutagenesis analyses allow us to provide a focus for understanding cellular responses to hypoxia and a target for the therapeutic manipulation.

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Structural Basis of the Disease-related Proteins: Target Oriented Structural Proteomics

  • Hwang, Kwang-Yeon;Lee, Tae-Gyu;Kim, Jin-Hwan;Jeon, Young-Ho;Seonggu Ro;Cho, Joong-Myung
    • 한국생물물리학회:학술대회논문집
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    • 한국생물물리학회 2003년도 정기총회 및 학술발표회
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    • pp.28-28
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    • 2003
  • To discover new drugs more quickly and more efficiently, pharmaceutical companies and biotechnology firms are increasingly turning to the genomics and the structural proteomics technologies. Structural-proteomics can provide a foundation for this through the determination and analysis for protein structure on a genomics scale. Among many structures determined by CGI, we will present with the representative examples drawn from our work on novel structures or complex structures of the disease-related proteins. The alpha subunit of Hypoxia-inducible factor (HIF) is targeted for degradation under normoxic conditions by an ubiquitin-ligase complex that recognizes a hydroxylated proline residue in HIF, Hydroxylation is catalysed by HIF prolyl 4-hydroxylases (HIFPH) which are Fe(II) and 2-oxoglutarate (2-OG) dependent oxygenases. Here, we discuss the first crystal structure of the catalytic domain of HIFPH in complexes, with the Fe(II)/2-OG at 1.8 ${\AA}$. These structures suggest that the L1 region (residues 236-253), which is also conserved in mammals, form a ‘lid’ that closes over the active site. The structural and mutagenesis analyses allow us to provide a focus for understanding cellular responses to hypoxia and a target for the therapeutic manipulation.

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형질전환체, Bacillus thuringiensis PT0529내에서 세가지 내독소 단백질 유전자들의 발현 특성 (Expression and Characterization of Three Types of $\delta$-Endotoxin Genes in Transformant, Bacillus thruingiensis PT0529)

  • 박현우;제연호
    • 한국잠사곤충학회지
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    • 제37권2호
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    • pp.176-180
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    • 1995
  • 나비목과 파리목 곤충에 독성을 보이는 B. thuringiensis NT0423을 수용체로 하여 형질전환된 B. thuringiensis PT0529에서 원래 수용체가 생성하는 내독소 단백질과 도입된 CryIVD 및 CytA 단백질들간의 발현 특성을 분석하기 위하여, B. thuringiensis PT0529에서 내독소 단백질들간의 발현을 성장 과정에 따라 투과 전자 현미경 관찰 및 단백질 전기영동으로 분석하였다. 그 결과, B. thuringiensis PT0529에서 내독소 단백질의 발현은 원래의 수용체 내독소 단백질보다 도입된 CryIVD와 CytA가 먼저 합성되었으며, 그 발현량에 있어서도 높게 나타났다. 또한, B. thuringiensis PT0529에서 세가지 내독소 단백질은 그들 자신의 고유 형태로 잘 발현되었으나, 수용체인 B. thuringiensis NT0423의 내독소 단백질은 그 크기에 있어서 다소 작게 관찰되었다. 따라서 형질전환체 내에서 도입된 내독소 단백질 유전자의 발현은 수용체의 내독소 단백질 유전자 발현에 영향을 받지 않는 반면 외부 유전자의 도입으로 인하여 수용체가 생성하는 내독소 단백질은 그 발현에 있어서 간섭을 받는 것으로 나타났다.

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