首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >SEROLOGICAL STUDIES ON THE FORMATION OF PROTEIN PARASPORAL INCLUSIONS IN BACILLUS THURINGIENSIS
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SEROLOGICAL STUDIES ON THE FORMATION OF PROTEIN PARASPORAL INCLUSIONS IN BACILLUS THURINGIENSIS

机译:苏云金杆菌蛋白质B草夹杂物形成的血清学研究

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摘要

A strain of Bacillus thuringiensis has been isolated, and methods have been developed for separation of the crystalline, parasporal inclusions in a pure form. Normal sporulation with concomitant crystal formation takes place when cells are incubated under suitable conditions in a nutrient free medium. Serological techniques have been used to study the origin and development of the crystals. Rabbit antisera have been prepared to a vegetative cell extract, suspensions of crystals, and a solution of crystal protein (obtained by alkali treatment of crystals). Tests have been carried out mainly by the Ouchterlony gel plate technique. Crystal protein solutions were found to be more active than suspensions of intact crystals both in reaction with, and in neutralization of, the crystal antibodies. Antisera to the vegetative cell extract gave no reaction with crystal protein. Ultrasonic extracts of cells taken before or during crystal formation gave no reaction with the crystal antibodies. Tests with alkali extracts of disrupted cells showed that the crystal antigen is absent in vegetative cells but arises during sporulation. The appearance of the antigen can be correlated with the formation and growth of the crystals as followed by examination of disrupted cell preparations under the electron microscope. It can be concluded that the crystalline protein inclusions do not arise from precursors in the same antigenic state.
机译:已经分离了苏云金芽孢杆菌的菌株,并且已经开发出用于分离纯形式的晶状,孢子旁夹杂物的方法。当细胞在合适的条件下在无营养的培养基中孵育时,会发生伴随结晶形成的正常孢子形成。血清学技术已被用于研究晶体的起源和发展。兔抗血清已制备为营养细胞提取物,晶体悬浮液和晶体蛋白溶液(通过对晶体进行碱处理而获得)。主要通过Ouchterlony凝胶板技术进行了测试。发现晶体蛋白溶液在与晶体抗体反应和中和中都比完整晶体的悬浮液更有活性。营养细胞提取物的抗血清未与晶体蛋白反应。在晶体形成之前或期间获取的细胞超声提取物未与晶体抗体反应。用破坏细胞的碱提取物进行的测试表明,营养细胞中不存在晶体抗原,但在孢子形成过程中会出现。抗原的出现可以与晶体的形成和生长相关,随后在电子显微镜下检查破坏的细胞制备物。可以得出结论,结晶蛋白内含物不是来自处于相同抗原状态的前体。

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