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RELATIONSHIPS BETWEEN TOBACCO MOSAIC VIRUS BIOSYNTHESIS AND THE NITROGEN METABOLISM OF THE HOST

机译:烟草花叶病毒生物合成与寄主氮代谢的关系

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摘要

1. Comparisons of the nitrogen content of TMV-infected and uninfected tobacco leaf discs at various times after inoculation show that virus synthesis is associated with a net increase in protein content. This excess protein is due to: (a) TMV, (b) an excess in insoluble protein which develops soon after inoculation and ends about 100 hours before cessation of TMV synthesis, and (c) an excess in soluble non-virus protein, which is variable in size and which only occurs during the time of virus synthesis. A deficiency in non-protein nitrogen occurs during the time when virus appears. 2. Isotope experiments with N15-labelled nutrient show that: (a) The bulk of TMV nitrogen is derived from the free ammonia of the host tissue. (b) Amino acid residues of TMV protein are not derived from the corresponding free amino acids in the host. (c) The appearance of TMV is preceded by the synthesis of an insoluble precursor of the virus which is then converted into TMV or some soluble intermediate protein. This effect is associated with a cell particulate which represents a small fraction of the total insoluble protein. (d) Infected tissue synthesizes de novo small amounts of soluble non-virus protein, which may represent intermediates in TMV synthesis. (e) Infected tissue fails to synthesize a rapidly turned-over soluble protein which is synthesized in comparable uninfected tissue. (f) TMV synthesis is preceded by a temporary enhancement of the metabolic stability of an insoluble protein component. 3. The results lead to the conclusion that TMV formation is due to diversion of some part of the host's protein-synthesizing apparatus from its normal course.
机译:1.接种后不同时间对TMV感染和未感染的烟叶圆盘的氮含量进行比较,结果表明病毒合成与蛋白质含量的净增加有关。这种过量的蛋白质是由于:(a)TMV,(b)过量的不溶性蛋白质,其在接种后很快形成并在TMV合成停止前约100小时结束,以及(c)过量的可溶性非病毒蛋白质,其大小可变,仅在病毒合成期间发生。病毒出现时,非蛋白质氮缺乏。 2.用N15标记的营养物进行的同位素实验表明:(a)大部分TMV氮均来自宿主组织的游离氨。 (b)TMV蛋白的氨基酸残基不是源自宿主中相应的游离氨基酸。 (c)在出现TMV之前,先合成病毒的不溶性前体,然后将其转化为TMV或某些可溶性中间蛋白。这种作用与细胞颗粒有关,细胞颗粒占总不溶蛋白的一小部分。 (d)感染的组织从头合成少量可溶性非病毒蛋白,这可能代表TMV合成的中间体。 (e)感染的组织不能合成在相当的未感染组织中合成的快速翻转的可溶性蛋白。 (f)在TMV合成之前,暂时增强不溶性蛋白质组分的代谢稳定性。 3.结果得出结论,TMV的形成是由于宿主蛋白质合成装置的某些部分偏离了其正常进程。

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