首页> 外文期刊>Biotechnology Journal: Healthcare,Nutrition,Technology >The Immunosuppressant Brasilicardin: Determination of the Biosynthetic Gene Cluster in the Heterologous Host Amycolatopsis japonicum
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The Immunosuppressant Brasilicardin: Determination of the Biosynthetic Gene Cluster in the Heterologous Host Amycolatopsis japonicum

机译:免疫抑制剂Brasilicardin:确定异源宿主Amycolatopsis的生物合成基因簇的测定

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摘要

Nocardia terpenica IFM 0406 is the producer of the immunosuppressants brasilicardins A-D. Brasilicardin is a promising compound because of its unique mode of action and its higher potency and reduced toxicity compared to today's standard drugs. However, production of brasilicardin is so far hampered as Nocardia terpenica IFM 0406 synthesizes brasilicardin in only low amounts and represents a human pathogen (biosafety level 2 BSL2). In order to achieve a safe and high yield production of brasilicardin A (BraA), the authors heterologously express the brasilicardin gene cluster in the nocardioform actinomycete Amycolatopsis japonicum (A. japonicum::bcaAB01), which is fast growing, genetically accessible and closely related to N. terpenica IFM 0406. In A. japonicum::bcaAB01, four brasilicardin congeners, intermediates of the BraA biosynthesis, are produced. Investigation of the genes flanking the previously defined brasilicardin biosynthetic gene cluster revealed two novel genes (bra0, bra12), which are involved in brasilicardin biosynthesis: bra12 encodes a transcriptional activator of the brasilicardin gene cluster. bra0 codes for a dioxygenase involved in methoxylation of brasilicardin. Based on this finding the authors are able to revise the proposed brasilicardin biosynthesis.
机译:Nocardia Terpenica IFM 0406是免疫抑制剂Brasilicardins A-D的生产者。巴西霉素是一个有希望的化合物,因为它与今天的标准药物相比其独特的作用和其较高效力和毒性降低。然而,由于Nocardia Terpenica IFM 0406仅用低量合成糖尿杆菌并代表一种人病原体(生物安全级2 BSL2),因此兔子的生产却受到阻碍。为了达到巴西霉素A(Braa)的安全和高产率,作者异乎寻常地表达Nocardioform放线菌杏仁糖尿病的肉豆蔻蛋白基因簇(A.paponicum :: bcaab01),其快速生长,转基因和密切相关对于N.Terpenica IFM 0406.在A. japonicum :: bcaab01中,产生四种肉豆蔻酰胺,生物合成的中间体。侧翼的侧翼所述基因的研究揭示了两种新基因(Bra0,Bra12),其参与BrasilicardIn生物合成:Bra12编码了糖尿病基因簇的转录活化剂。用于甲氧化素的二恶英酶的BRA0代码。基于这一发现,作者能够修改拟议的Brasilicardin生物合成。

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