首页> 外文期刊>Virology >The Trichoplusia ni single nucleopolyhedrovirus tn79 gene encodes a functional sulfhydryl oxidase enzyme that is able to support the replication of Autographa califomica multiple nucleopolyhedrovirus lacking the sulfhydryl oxidase ac92 gene
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The Trichoplusia ni single nucleopolyhedrovirus tn79 gene encodes a functional sulfhydryl oxidase enzyme that is able to support the replication of Autographa califomica multiple nucleopolyhedrovirus lacking the sulfhydryl oxidase ac92 gene

机译:Trichoplusia ni单核多角体病毒tn79基因编码一种功能性巯基氧化酶,该酶能够支持缺少巯基氧化酶ac92基因的Autographa califomica多核多角体病毒的复制。

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摘要

The Autographa califomica multiple nucleopolyhedrovirus ac92 is a conserved baculovirus gene with homology to flavin adenine dinucleotide-linked sulfhydryl oxidases. Its product, Ac92, is a functional sulfhydryl oxidase. Deletion of ac92 results in almost negligible levels of budded virus (BV) production, defects in occlusion-derived virus (ODV) co-envelopment and their inefficient incorporation into occlusion bodies. To determine the role of sulfhydryl oxidation in the production of BV, envelopment of nucleocapsids, and nucleocapsid incorporation into occlusion bodies, the Trichoplusia ni single nucleopolyhedrovirus ortholog, tn79, was substituted for ac92. Tn79 was found to be an active sulfhydryl oxidase that substituted for Ac92, resulting in the production of infectious BV, albeit about 10-fold less than an ac92-containing virus. Tn79 rescued defects in ODV morphogenesis caused by a lack of ac92. Active Tn79 sulfhydryl oxidase activity is required for efficient BV production, ODV envelopment, and their subsequent incorporation into occlusion bodies in the absence of ac92.
机译:加利福尼亚Autographa多核多角体病毒ac92是一种保守的杆状病毒基因,与黄素腺嘌呤二核苷酸连接的巯基氧化酶具有同源性。它的产物Ac92是功能性巯基氧化酶。删除ac92会导致芽接病毒(BV)产生的水平几乎可以忽略不计,闭塞衍生病毒(ODV)共同包封的缺陷以及将其无效地掺入闭塞体中的情况。为了确定巯基氧化在BV产生,核衣壳包封和核衣壳掺入闭塞体中的作用,用Trichoplusia ni ni单核多角体病毒直系同源物tn79代替了ac92。发现Tn79是一种能取代Ac92的活性巯基氧化酶,可产生传染性BV,尽管比含ac92的病毒少10倍。 Tn79挽救了由于缺乏ac92导致的ODV形态发生中的缺陷。有效的BV产生,ODV包封以及随后在不存在ac92的情况下将其掺入闭塞体中需要有效的Tn79巯基氧化酶活性。

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