Cloning of a new Bacillus thuringiensis cry1I-type crystal protein gene

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dc.contributor.authorSoo Keun Choi-
dc.contributor.authorByung Sik Shin-
dc.contributor.authorEun Mee Kong-
dc.contributor.authorHyune Mo Rho-
dc.contributor.authorSeung Hwan Park-
dc.date.accessioned2017-04-19T08:57:08Z-
dc.date.available2017-04-19T08:57:08Z-
dc.date.issued2000-
dc.identifier.issn0343-8651-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/5121-
dc.description.abstractA new cry1I-type gene, cry1Id1, was cloned from a B. thuringiensis isolate, and its nucleotide sequence was determined. The deduced amino acid sequence of Cry1Id1 is 89.7%, 87.2%, and 83.4% identical to the Cry1Ia, Cry1Ib, and Cry1Ic proteins, respectively. The upstream sequence of the cry1Id1 structural gene was not functional as promoter in B. subtilis. The Cry1Id1 protein, purified from recombinant E. coli cells, had a toxicity comparable to that of Cry1Ia against Plutella xylostella, but it was significantly less active than Cry1Ia against Bombyx mori. Cry1Id1 was not active against the coleopteran insect, Agelastica coerulea.-
dc.publisherSpringer-
dc.titleCloning of a new Bacillus thuringiensis cry1I-type crystal protein gene-
dc.title.alternativeCloning of a new Bacillus thuringiensis cry1I-type crystal protein gene-
dc.typeArticle-
dc.citation.titleCurrent Microbiology-
dc.citation.number1-
dc.citation.endPage69-
dc.citation.startPage65-
dc.citation.volume41-
dc.contributor.affiliatedAuthorSoo Keun Choi-
dc.contributor.affiliatedAuthorSeung Hwan Park-
dc.contributor.alternativeName최수근-
dc.contributor.alternativeName신병식-
dc.contributor.alternativeName공은미-
dc.contributor.alternativeName노현모-
dc.contributor.alternativeName박승환-
dc.identifier.bibliographicCitationCurrent Microbiology, vol. 41, no. 1, pp. 65-69-
dc.identifier.doi10.1007/s002840010093-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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