Characterization of a novel mosquitocidal strain of Bacillus thuringiensis serovar aizawai which harbors a rolling-circle replication plasmid, pBt1-3

被引:0
|
作者
Liu, Qin [1 ]
Roh, Jong Yul [2 ]
Wang, Yong [3 ]
Choi, Jae Young [4 ]
Tao, Xue Ying [1 ]
Jin, Byung Rae [5 ]
Je, Yeon Ho [1 ]
机构
[1] Seoul Natl Univ, Coll Agr & Life Sci, Dept Agr Biotechnol, Seoul 151742, South Korea
[2] Korea Natl Inst Hlth, Div Med Entomol, Chungbuk 363951, South Korea
[3] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Peoples R China
[4] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 151742, South Korea
[5] Dong A Univ, Coll Nat Resources & Life Sci, Pusan 604714, South Korea
关键词
Bacillus thuringiensis; Aizawai; cry2A; Cryptic plasmid; pBt1-3; RCR group VI; NUCLEOTIDE-SEQUENCE; CRYSTAL PROTEINS; CAPTURE SYSTEM; CLONING; INSECT; PESTS;
D O I
10.1016/j.aspen.2013.03.004
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Bacillus thuringiensis 1-3, isolated from a Korean soil sample, was determined to belong to ssp. aizawai (H7) type by an H antiserum agglutination test, and produced bipyramidal-shaped crystal proteins with a molecular weight of 130 kDa. PCR analysis with specific cry gene primers showed that B. thuringiensis 1-3 contained cry1Aa, cry1Ab, cry1C, cry1D and cry2A genes, differing from that of serovar of aizawai (reference strain) which contains cry1Aa, cry1Ab, cry1C and cry1D genes. In contrast to the reference strain, B. thuringiensis aizawai showed insecticidal activity against Plutella xylostella larvae, the B. thuringiensis 1-3 showed insecticidal activity against not only P. xylostella, but also Aedes aegypti, owing to its Cry2A crystal protein. In this study, we modified the plasmid capture system (PCS) through in vitro transposition to clone small cryptic plasmids from B. thuringiensis 1-3. Fifty-three clones were acquired, and their sizes were approximately 10 kb. Based on the sequence analysis, they were classified into four groups, showing similarities with four known B. thuringiensis plasmids, pGI3, pBMB175, pGI1 and pGI2, respectively. One of the pGI3-like clones, pBt1-3, was fully sequenced, and its putative open reading frames (ORFs), Rep-protein, double-strand origin of replication (dso), single-strand origin of replication (sso), have been identified. The structure of pBt1-3 showed high similarity with pGI3, which is of the rolling-circle replication (RCR) group VI family. (c) Korean Society of Applied Entomology, Taiwan Entomological Society and Malaysian Plant Protection Society, 2013. Published by Elsevier B.V. All rights reserved.
引用
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页码:257 / 261
页数:5
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