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生物膜光刻技术通过光遗传学黏附蛋白表达实现高分辨率细胞图案化。

Biofilm Lithography enables high-resolution cell patterning via optogenetic adhesin expression.

机构信息

Department of Bioengineering, Stanford University, Stanford, CA 94305.

Department of Bioengineering, Stanford University, Stanford, CA 94305

出版信息

Proc Natl Acad Sci U S A. 2018 Apr 3;115(14):3698-3703. doi: 10.1073/pnas.1720676115. Epub 2018 Mar 19.

Abstract

Bacterial biofilms represent a promising opportunity for engineering of microbial communities. However, our ability to control spatial structure in biofilms remains limited. Here we engineer with a light-activated transcriptional promoter (pDawn) to optically regulate expression of an adhesin gene (Ag43). When illuminated with patterned blue light, long-term viable biofilms with spatial resolution down to 25 μm can be formed on a variety of substrates and inside enclosed culture chambers without the need for surface pretreatment. A biophysical model suggests that the patterning mechanism involves stimulation of transiently surface-adsorbed cells, lending evidence to a previously proposed role of adhesin expression during natural biofilm maturation. Overall, this tool-termed "Biofilm Lithography"-has distinct advantages over existing cell-depositing/patterning methods and provides the ability to grow structured biofilms, with applications toward an improved understanding of natural biofilm communities, as well as the engineering of living biomaterials and bottom-up approaches to microbial consortia design.

摘要

细菌生物膜为微生物群落的工程设计提供了一个很有前景的机会。然而,我们控制生物膜空间结构的能力仍然有限。在这里,我们利用光激活转录启动子 (pDawn) 来光学调控黏附素基因 (Ag43) 的表达。当用图案化的蓝光照射时,无需表面预处理,就可以在各种基底上和封闭的培养室内形成具有空间分辨率低至 25μm 的长期存活生物膜。生物物理模型表明,图案形成机制涉及对瞬态表面吸附细胞的刺激,这为黏附素表达在自然生物膜成熟过程中的先前提出的作用提供了证据。总的来说,这种被称为“生物膜光刻”的工具相对于现有的细胞沉积/图案化方法具有明显的优势,并提供了生长结构生物膜的能力,可应用于更好地理解自然生物膜群落,以及设计活体生物材料和自下而上的微生物联合体的工程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d044/5889658/c48e10aad752/pnas.1720676115fig01.jpg

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