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用于跨拟杆菌属物种异源蛋白分泌的分子工具包。

A molecular toolkit for heterologous protein secretion across Bacteroides species.

机构信息

Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, IL, USA.

Chan Zuckerberg Biohub, Chicago, IL, USA.

出版信息

Nat Commun. 2024 Nov 11;15(1):9741. doi: 10.1038/s41467-024-53845-7.

Abstract

Bacteroides species are abundant, prevalent, and stable members of the human gut microbiota, making them a promising chassis for developing long-term interventions for chronic diseases. Engineering Bacteroides as in situ bio-factories, however, requires efficient protein secretion tools, which are currently lacking. Here, we systematically investigate methods to enable heterologous protein secretion in Bacteroides. We identify a collection of secretion carriers that can export functional proteins across multiple Bacteroides species at high titers. To understand the mechanistic drivers of Bacteroides secretion, we characterize signal peptide sequence features, post-secretion extracellular fate, and the size limit of protein cargo. To increase titers and enable flexible control of protein secretion, we develop a strong, self-contained, inducible expression circuit. Finally, we validate the functionality of our secretion carriers in vivo in a mouse model. This toolkit promises to enable expanded development of long-term living therapeutic interventions for chronic gastrointestinal disease.

摘要

拟杆菌是人类肠道微生物群中丰富、普遍且稳定的成员,因此它们是开发慢性疾病长期干预措施的有前途的底盘。然而,将拟杆菌工程化为原位生物工厂需要有效的蛋白质分泌工具,而目前这些工具还很缺乏。在这里,我们系统地研究了在拟杆菌中实现异源蛋白质分泌的方法。我们鉴定了一组分泌载体,这些载体可以在多种拟杆菌物种中以高滴度水平分泌功能蛋白。为了了解拟杆菌分泌的机制驱动因素,我们对信号肽序列特征、分泌后细胞外命运以及蛋白质货物的大小限制进行了表征。为了提高产量并实现蛋白质分泌的灵活控制,我们开发了一个强大、自包含、可诱导的表达回路。最后,我们在小鼠模型中验证了我们的分泌载体的功能。该工具包有望为慢性胃肠道疾病的长期治疗干预措施的开发提供更大的发展空间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0add/11554821/0c81f79d2596/41467_2024_53845_Fig1_HTML.jpg

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