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重组杆状病毒在昆虫细胞中表达的细菌晶体蛋白的杀虫活性。

Insecticidal activity of a bacterial crystal protein expressed by a recombinant baculovirus in insect cells.

机构信息

Department of Virology, Agricultural University Wageningen, P.O. Box 8045, 6700 EM Wageningen, and Center for Plant Breeding Research, P.O. Box 16, 6700 AA Wageningen, The Netherlands.

出版信息

Appl Environ Microbiol. 1990 Sep;56(9):2764-70. doi: 10.1128/aem.56.9.2764-2770.1990.

Abstract

Baculoviruses are insect pathogens with a relatively slow speed of action, and this has limited their use as control agents of insect pests. Introduction into baculoviruses of genes which code for proteins interfering specifically with insect metabolism or metamorphosis, such as toxins, hormones, and enzymes, may enhance the pathogenicity of these viruses. The complete insecticidal crystal protein gene cryIA(b) of Bacillus thuringiensis subsp. aizawai 7.21 was engineered into the nuclear polyhedrosis virus of Autographa californica (AcNPV) in place of the polyhedrin gene. In infected Spodoptera frugiperda cells, the cryIA(b) gene was expressed at a high level without interference with AcNPV production. The crystal protein was found in the cytoplasm of S. frugiperda cells, mainly as large crystals with an ultrastructure similar to that of B. thuringiensis crystals. Infected-cell extracts inhibited feeding of the large cabbage white Pieris brassicae. The toxicity of the crystal protein expressed by AcNPV recombinants was comparable with that of the crystal protein expressed by a corresponding Escherichia coli recombinant.

摘要

杆状病毒是一种作用相对缓慢的昆虫病原体,这限制了它们作为昆虫害虫防治剂的使用。将编码特异性干扰昆虫代谢或变态的蛋白质(如毒素、激素和酶)的基因引入杆状病毒中,可能会增强这些病毒的致病性。苏云金芽孢杆菌亚种 aizawai 7.21 的完整杀虫晶体蛋白基因 cryIA(b)被工程改造到加利福尼亚粘虫核多角体病毒(AcNPV)中,取代了多角体蛋白基因。在感染的夜蛾细胞中,cryIA(b)基因在不干扰 AcNPV 产生的情况下高水平表达。晶体蛋白存在于 S. frugiperda 细胞的细胞质中,主要呈大晶体状,其超微结构与苏云金芽孢杆菌晶体相似。感染细胞提取物抑制了大菜粉蝶的摄食。由 AcNPV 重组体表达的晶体蛋白的毒性与相应的大肠杆菌重组体表达的晶体蛋白的毒性相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c15/184840/89cabf66aec2/aem00090-0186-a.jpg

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