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Generation of a Highly Attenuated Strain of Pseudomonas Aeruginosa for Commercial Production of Alginate.

Meagan E. Valentine,Brandon D. Kirby, Thomas R. Withers,Shannon L. Johnson,Timothy E. Long,Youai Hao,Joseph S. Lam, Richard M. Niles,Hongwei D. Yu

Microbial Biotechnology(2019)

Progenesis Technol LLC | Los Alamos Natl Lab | Marshall Univ | Univ Guelph

Cited 40|Views43
Abstract
Summary Alginate is an important polysaccharide that is commonly used as a gelling agent in foods, cosmetics and healthcare products. Currently, all alginate used commercially is extracted from brown seaweed. However, with environmental changes such as increasing ocean temperature and the increasing number of biotechnological uses of alginates with specific properties, there is an emerging need for more reliable and customizable sources of alginate. An alternative to seaweed for alginate production is Pseudomonas aeruginosa, a common Gram‐negative bacterium that can form alginate‐containing biofilms. However, P. aeruginosa is an opportunistic pathogen that can cause life‐threatening infections in immunocompromised patients. Therefore, we sought to engineer a non‐pathogenic P. aeruginosa strain that is safe for commercial production of alginate. Using a homologous recombination strategy, we sequentially deleted five key pathogenicity genes from the P. aeruginosa chromosome, resulting in the marker‐free strain PGN5. Intraperitoneal injection of mice with PGN5 resulted in 0% mortality, while injection with wild‐type P. aeruginosa resulted in 95% mortality, providing evidence that the systemic virulence of PGN5 is highly attenuated. Importantly, PGN5 produces large amounts of alginate in response to overexpression of MucE, an activator of alginate biosynthesis. The alginate produced by PGN5 is structurally identical to alginate produced by wild‐type P. aeruginosa, indicating that the alginate biosynthetic pathway remains functional in this modified strain. The genetic versatility of P. aeruginosa will allow us to further engineer PGN5 to produce alginates with specific chemical compositions and physical properties to meet different industrial and biomedical needs.
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要点】:该研究通过基因工程手段创建了一种非致病性的大肠杆菌株PGN5,用于商业生产结构与天然相同的高安全性藻酸盐,其通过体内注射实验证明了该菌株的高度减毒特性,并展示了其能响应基因过表达产生大量藻酸盐的能力。

方法】:采用同源重组策略,连续删除了五个关键的致病基因。

实验】:通过小鼠腹腔注射实验,比较了PGN5和野生型P. aeruginosa的致死率;通过过表达MucE基因实现了PGN5产生大量藻酸盐,并确认了其结构与野生型一致。使用的数据集未在摘要中提及。