Hay Iain D, Du Jinping, Burr Natalie, Rehm Bernd H A
Polybatics Ltd., Palmerston North, New Zealand.
Polybatics Ltd., Palmerston North, New Zealand Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Appl Environ Microbiol. 2015 Jan;81(1):282-91. doi: 10.1128/AEM.02595-14. Epub 2014 Oct 24.
Proof of concept for the in vivo bacterial production of a polyester resin displaying various customizable affinity protein binding domains is provided. This was achieved by engineering various protein binding domains into a bacterial polyester-synthesizing enzyme. Affinity binding domains based on various structural folds and derived from molecular libraries were used to demonstrate the potential of this technique. Designed ankyrin repeat proteins (DARPins), engineered OB-fold domains (OBodies), and VHH domains from camelid antibodies (nanobodies) were employed. The respective resins were produced in a single bacterial fermentation step, and a simple purification protocol was developed. Purified resins were suitable for most lab-scale affinity chromatography purposes. All of the affinity domains tested produced polyester beads with specific affinity for the target protein. The binding capacity of these affinity resins ranged from 90 to 600 nmol of protein per wet gram of polyester affinity resin, enabling purification of a recombinant protein target from a complex bacterial cell lysate up to a purity level of 96% in one step. The polyester resin was efficiently produced by conventional lab-scale shake flask fermentation, resulting in bacteria accumulating up to 55% of their cellular dry weight as polyester. A further proof of concept demonstrating the practicality of this technique was obtained through the intracellular coproduction of a specific affinity resin and its target. This enables in vivo binding and purification of the coproduced "target protein." Overall, this study provides evidence for the use of molecular engineering of polyester synthases toward the microbial production of specific bioseparation resins implementing previously selected binding domains.
本文提供了在体内细菌生产展示各种可定制亲和蛋白结合域的聚酯树脂的概念验证。这是通过将各种蛋白结合域工程化到细菌聚酯合成酶中来实现的。基于各种结构折叠并源自分子文库的亲和结合域被用于证明该技术的潜力。使用了设计的锚蛋白重复蛋白(DARPins)、工程化的OB折叠域(OBodies)以及骆驼科抗体的VHH域(纳米抗体)。各自的树脂在单个细菌发酵步骤中产生,并开发了一种简单的纯化方案。纯化后的树脂适用于大多数实验室规模的亲和色谱目的。所有测试的亲和域都产生了对目标蛋白具有特异性亲和力的聚酯珠。这些亲和树脂的结合能力为每湿克聚酯亲和树脂90至600 nmol蛋白质,能够从复杂的细菌细胞裂解物中一步纯化重组蛋白靶标,纯度高达96%。聚酯树脂通过传统的实验室规模摇瓶发酵有效生产,导致细菌积累的聚酯占其细胞干重的55%。通过细胞内共生产特定的亲和树脂及其靶标,获得了进一步证明该技术实用性的概念验证。这使得能够在体内结合和纯化共生产的“靶标蛋白”。总体而言,本研究为利用聚酯合酶的分子工程实现微生物生产实施先前选定结合域的特定生物分离树脂提供了证据。