Sun Yunjun, Wei Wei, Ding Xuezhi, Xia Liqiu, Yuan Zhiming
Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, People's Republic of China.
Arch Microbiol. 2007 Oct;188(4):327-32. doi: 10.1007/s00203-007-0252-7. Epub 2007 May 22.
The association of 20 kb heterologous DNA fragments with the parasporal crystals from native and recombinant Bacillus thuringiensis strains was analyzed, respectively. The cry2Aa10 gene cloned in plasmid pHC39 was transformed into B. thuringiensis subsp. kurstaki strains Cry B and HD73, producing recombinant strains Cry B(pHC39) and HD73(pHC39). SDS-PAGE and scanning electron microscopy analyses demonstrated that the recombinant Cry B(pHC39) produced cuboidal crystals of Cry2Aa10 protoxin, while recombinant HD73(pHC39) produced both bipyramidal crystals of Cry1Ac1 protoxin and cuboidal crystals of Cry2Aa10 protoxin. Bioassay results proved that recombinant HD73(pHC39) showed higher insecticidal activity to Helicoverpa armigera than Cry B(pHC39). It was found that 20 kb DNA fragments were present in bipyramidal and cuboidal crystals from both native and recombinant strains, and the 20 kb heterologous DNAs contained chromosome-specific and resident large plasmid-borne DNA fragments, suggesting the 20 kb heterologous DNA fragment embodied in crystals came randomly from the bacterial chromosomal and plasmid genome. This was the first investigation devoted exclusively on the origin of 20 kb DNA fragments in the parasporal crystals of B. thuringiensis. The data provides a basis for further investigation of the origin of 20 kb DNAs in the crystals and the interaction of DNA and protoxins.
分别分析了来自天然和重组苏云金芽孢杆菌菌株的伴孢晶体与20 kb异源DNA片段的关联。将克隆于质粒pHC39中的cry2Aa10基因转化到苏云金芽孢杆菌库斯塔克亚种菌株Cry B和HD73中,产生重组菌株Cry B(pHC39)和HD73(pHC39)。SDS-PAGE和扫描电子显微镜分析表明,重组菌株Cry B(pHC39)产生Cry2Aa10原毒素的立方晶体,而重组菌株HD73(pHC39)既产生Cry1Ac1原毒素的双锥晶体,也产生Cry2Aa10原毒素的立方晶体。生物测定结果证明,重组菌株HD73(pHC39)对棉铃虫的杀虫活性高于Cry B(pHC39)。研究发现,天然菌株和重组菌株的双锥晶体和立方晶体中均存在20 kb DNA片段,且这20 kb异源DNA包含染色体特异性和位于大质粒上的DNA片段,表明晶体中所含的20 kb异源DNA片段随机来自细菌染色体和质粒基因组。这是首次专门针对苏云金芽孢杆菌伴孢晶体中20 kb DNA片段来源的研究。这些数据为进一步研究晶体中20 kb DNA的来源以及DNA与原毒素的相互作用提供了依据。