Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseскороОткрытый API экосистемы
Латиница
Статья

Expression of a foreign gene by cysteine proteinase null recombinant baculovirus

Olga LihoradovaInstitute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent, 100170, UzbekistanI. D. OgayInstitute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent, 100170, UzbekistanM. M. PodpisnovaInstitute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent, 100170, UzbekistanJeffrey M. SlackGreat Lakes Forestry Center, Canadian Forestry Service Natural Resources Canada, Sault Ste. Marie, P6A 2E5, CanadaShakhnoza S. AzimovaInstitute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent, 100170, Uzbekistan
Molecular Biologyjournal2008en
ABI

Аннотация

The baculovirus expression vector systems (BEVS) are broadly used for producing foreign proteins in lepidopteran larvae. Most commercial BEVS are engineered to insert foreign genes into the polyhedrin (polh) locus and lack the polh gene. These viruses cannot produce occlusion bodies and are inconvenient for per os inoculation of larvae. Current knowledge in baculovirus genomics makes it possible to engineer BEVS into other parts of the virus genome. In our work, we have expressed recombinant M-HBsAg (middle surface antigen of human hepatitis B) in the baculovirus construct, rBmNPV-Deltav-cath-M-HBsAg, inserting foreign gene into the v-cath locus of the Bombyx mori nucleopolyhedrovirus (BmNPV) such that the v-cath gene is deleted and the native polh gene is retained. Silkworm larvae were infected per os and M-HBsAg was observed to be abundantly produced at a very late stage of infection.

Темы

Идентификаторы

Цитирования и источники

Показатели — AkademScholar · Скоро