利用组合策略挖掘声纳米结构生物合成基因簇。

Wei Liu, Tingting Liu, Shenxi Huang, Fei Yan, Jian-Zhong Liu
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摘要

微生物产生的气体囊泡(GVs)是一种基因工程的、充满空气的蛋白质纳米结构,在超声成像和超声介导的药物传递中有着广泛的应用。然而,由于受到形状和大小的限制,它们中的大多数难以被临床超声仪成像,这限制了它们在生物医学上的应用。本研究利用大肠杆菌中巨芽孢杆菌的辅助基因簇和Serratia sp. ATCC 39006的结构基因簇的杂交基因簇,合成了一个宽度约为70 nm,长度约为100 nm的新型基因编码气体囊泡,并将其命名为ARGS1B。这种新型的gv可以在细菌中稳定地产生,并且可以通过临床超声仪在体内和体外成像。此外,通过点饱和突变可以很容易地设计出不同粒径的纳米结构,扩大了gv的来源,并为gv的生物合成机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Excavation of acoustic nanostructures biosynthesis gene clusters by combinatorial strategy.

Gas vesicles (GVs) produced by microorganisms are genetically engineered, air-filled protein nanostructures that have widespread applications in ultrasound imaging and ultrasound-mediated drug delivery. However, constrained by the shape and size, most of them are difficult to be imaged by clinical ultrasound machines, which limits their biomedical applications. Here, we constructed a hybrid gene cluster of the structural gene cluster from Serratia sp. ATCC 39006 and the accessory gene cluster from Bacillus megaterium in Escherichia coli to synthesize a novel gene-encoded gas vesicle with a width of approximately 70 nm and a length of about 100 nm, using a synthetic biology strategy, termed as ARGS1B. This new type of GVs can be stably produced in bacteria and is able to be imaged by clinical ultrasound machines in vivo and in vitro. Furthermore, the novel nanostructure can be easily engineered for different particle sizes through point saturation mutation, expanding the sources of GVs and providing new insights into the biosynthesis mechanism of GVs.

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