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在 90 天内制造 10 个分子的压力测试:对生物学工程方法的外部评估。

A Pressure Test to Make 10 Molecules in 90 Days: External Evaluation of Methods to Engineer Biology.

机构信息

The Foundry , 75 Ames Street , Cambridge , Massachusetts 02142 , United States.

Broad Institute of MIT and Harvard , Cambridge , Massachusetts 02142 , United States.

出版信息

J Am Chem Soc. 2018 Mar 28;140(12):4302-4316. doi: 10.1021/jacs.7b13292. Epub 2018 Mar 16.

Abstract

Centralized facilities for genetic engineering, or "biofoundries", offer the potential to design organisms to address emerging needs in medicine, agriculture, industry, and defense. The field has seen rapid advances in technology, but it is difficult to gauge current capabilities or identify gaps across projects. To this end, our foundry was assessed via a timed "pressure test", in which 3 months were given to build organisms to produce 10 molecules unknown to us in advance. By applying a diversity of new approaches, we produced the desired molecule or a closely related one for six out of 10 targets during the performance period and made advances toward production of the others as well. Specifically, we increased the titers of 1-hexadecanol, pyrrolnitrin, and pacidamycin D, found novel routes to the enediyne warhead underlying powerful antimicrobials, established a cell-free system for monoterpene production, produced an intermediate toward vincristine biosynthesis, and encoded 7802 individually retrievable pathways to 540 bisindoles in a DNA pool. Pathways to tetrahydrofuran and barbamide were designed and constructed, but toxicity or analytical tools inhibited further progress. In sum, we constructed 1.2 Mb DNA, built 215 strains spanning five species ( Saccharomyces cerevisiae, Escherichia coli, Streptomyces albidoflavus, Streptomyces coelicolor, and Streptomyces albovinaceus), established two cell-free systems, and performed 690 assays developed in-house for the molecules.

摘要

集中式基因工程设施,或“生物工厂”,有潜力设计出能够满足医学、农业、工业和国防领域新出现需求的生物体。该领域的技术进步迅速,但很难评估当前的能力或确定各个项目之间的差距。为此,我们的工厂接受了一项限时“压力测试”,在 3 个月的时间内,我们要构建能够生产 10 种我们事先不知道的分子的生物体。通过应用多种新方法,我们在 10 个目标中有 6 个目标在规定的时间内生产出了所需的分子或与其密切相关的分子,并为其他目标的生产也取得了进展。具体来说,我们提高了 1-十六醇、吡咯并[1,2-a]嘧啶和 pacidamycin D 的产量,找到了新型途径来合成具有强大抗菌活性的烯二炔弹头,建立了萜烯生产的无细胞体系,生产了长春新碱生物合成的中间体,并在 DNA 池中编码了 7802 条可单独检索的途径到 540 条双吲哚。设计并构建了四氢呋喃和 barbamide 的途径,但毒性或分析工具抑制了进一步的进展。总之,我们构建了 1.2Mb 的 DNA,构建了跨越五个物种(酿酒酵母、大肠杆菌、白色链霉菌、变铅青链霉菌和白色链霉菌)的 215 个菌株,建立了两个无细胞体系,并进行了 690 次我们内部开发的分子检测。

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