Enhanced Astaxanthin Production in Escherichia coli via Morphology and Oxidative Stress Engineering.
Qian LuJian-Zhong LiuPublished in: Journal of agricultural and food chemistry (2019)
Astaxanthin is a carotenoid of high commercial value because of its excellent antioxidative, anti-inflammatory, and anticancer properties. Here, we developed a novel strategy for improving the production of astaxanthin via morphology and oxidative stress engineering. First, we identified the morphology-/membrane- and oxidative stress-related genes, which should be knocked down, using the CRISPRi system. Deleting the morphology-/membrane-related genes (lpp and bamB) and the oxidative stress-related genes (uspE and yggE) generated longer and larger cells with higher reactive oxygen species (ROS) levels, thus enhancing the production of astaxanthin and decreasing cell growth. To not only improve cell growth but also obtain longer and larger cells with higher ROS levels, a complementary expression system using a temperature-sensitive plasmid was established. Complementarily expressing the morphology-/membrane-related genes (lpp and bamB) and the oxidative stress-related genes (uspE and yggE) further improved the production of astaxanthin to 11.92 mg/g dry cell weight in shake flask cultures.
Keyphrases
- oxidative stress
- induced apoptosis
- dna damage
- reactive oxygen species
- escherichia coli
- diabetic rats
- ischemia reperfusion injury
- endoplasmic reticulum stress
- anti inflammatory
- cell death
- cell cycle arrest
- signaling pathway
- body mass index
- single cell
- mesenchymal stem cells
- weight loss
- cell proliferation
- pseudomonas aeruginosa
- long non coding rna
- stem cells
- cystic fibrosis
- multidrug resistant
- cell therapy
- bone marrow