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系统部件转移通过扩展模块化工具包至不同细菌。

Systematic Part Transfer by Extending a Modular Toolkit to Diverse Bacteria.

机构信息

Life Sciences and Bioengineering Center, Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts 01605, United States.

出版信息

ACS Synth Biol. 2023 Jul 21;12(7):2061-2072. doi: 10.1021/acssynbio.3c00104. Epub 2023 Jun 9.

Abstract

It is impractical to develop a new parts collection for every potential host organism. It is well-established that gene expression parts, like genes, are qualitatively transferable, but there is little quantitative information defining transferability. Here, we systematically quantified the behavior of a parts set across multiple hosts. To do this, we developed a broad host range (BHR) plasmid system compatible with the large, modular CIDAR parts collection for , which we named openCIDAR. This enabled testing of a library of DNA constructs across the Pseudomonadota─, , , and . Part performance was evaluated with a standardized characterization procedure that quantified expression in terms of molecules of equivalent fluorescein (MEFL), an objective unit of measure. The results showed that the CIDAR parts enable graded gene expression across all organisms─meaning that the same parts can be used to program , , , and . Most parts had a similar expression trend across hosts, although each organism had a different average gene expression level. The variability is enough that to achieve the same MEFL in a different organism, a lookup table is required to translate a design from one host to another. To identify truly divergent parts, we applied linear regression to a combinatorial set of promoters and ribosome binding sites, finding that the promoter J23100 behaves very differently in than in the other hosts. Thus, it is now possible to evaluate any CIDAR compatible part in three other hosts of interest, and the diversity of these hosts implies that the collection will also be compatible with many other Proteobacteria (Pseudomonadota). Furthermore, this work defines an approach to generalize modular synthetic biology parts sets beyond a single host, implying that only a few parts sets may be needed to span the tree of life. This will accelerate current efforts to engineer diverse species for environmental, biotechnological, and health applications.

摘要

开发针对每个潜在宿主生物的全新元件集是不切实际的。基因表达元件与基因一样,在质量上是可转移的,这已得到充分证实,但关于可转移的定量信息却很少。在这里,我们系统地量化了一套元件在多个宿主中的表现。为此,我们开发了一个广泛宿主范围(BHR)质粒系统,与大型模块化 CIDAR 元件集兼容,我们将其命名为 openCIDAR。这使得我们可以在 Pseudomonadota 属的多个物种中测试 DNA 文库—— 、 、 、 。使用标准化的特征描述程序对元件性能进行评估,该程序根据等效荧光素分子(MEFL)来量化表达水平,这是一种客观的度量单位。结果表明,CIDAR 元件可在所有生物中实现基因表达的梯度变化——这意味着相同的元件可用于编程 、 、 、 。尽管每个生物的平均基因表达水平不同,但大多数元件在宿主间具有相似的表达趋势。这种可变性足以说明,为了在不同的生物中达到相同的 MEFL,需要一个查找表来将设计从一个宿主转换到另一个宿主。为了识别真正的差异元件,我们对一组组合启动子和核糖体结合位点进行了线性回归分析,发现启动子 J23100 在 中的表现与其他宿主非常不同。因此,现在可以在另外三个感兴趣的宿主中评估任何与 CIDAR 兼容的元件,而这些宿主的多样性意味着该元件集也将与许多其他 Proteobacteria(Pseudomonadota)兼容。此外,这项工作定义了一种将模块化合成生物学元件集推广到单个宿主之外的方法,这意味着可能只需要几个元件集就可以涵盖生命之树。这将加速当前为环境、生物技术和健康应用而对不同物种进行工程设计的努力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0616/10367128/5c85aac2b022/sb3c00104_0001.jpg

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