Ham Sion, Cho Do-Hyun, Oh Suk Jin, Hwang Jeong Hyeon, Kim Hyun Jin, Shin Nara, Ahn Jungoh, Choi Kwon-Young, Bhatia Shashi Kant, Yang Yung-Hun
Department of Biological Engineering, College of Engineering, Konkuk University, the Republic of Korea.
Biotechnology Process Engineering Center, Korea Research Institute Bioscience Biotechnology (KRIBB), the Republic of Korea.
J Biotechnol. 2023 Mar 20;366:1-9. doi: 10.1016/j.jbiotec.2023.02.008. Epub 2023 Feb 26.
Indigo dye is an organic compound with a distinctive blue color. Most of the indigo currently used in industry is produced via chemical synthesis, which generates a large amount of wastewater. Therefore, several studies have recently been conducted to find ways to produce indigo eco-friendly using microorganisms. Here, we produced indigo using recombinant Escherichia coli with both an indigo-producing plasmid and a cyclopropane fatty acid (CFA)-regulating plasmid. The CFA-regulating plasmid contains the cfa gene, and its expression increases the CFA composition of the phospholipid fatty acids of the cell membrane. Overexpression of cfa showed cytotoxicity resistance of indole, an intermediate product formed during the indigo production process. This had a positive effect on indigo production and cfa originated from Pseudomonas sp. B 14-6 was used. Optimal conditions for indigo production were determined by adjusting the expression strain, culture temperature, shaking speed, and isopropyl β-D-1-thiogalactopyranoside concentration. Treatment with Tween 80 at a particular concentration to increase the permeability of the cell membrane had a positive effect on indigo production. The strain with the CFA plasmid produced 4.1 mM of indigo after 24 h of culture and produced 1.5-fold higher indigo than the control strain without the CFA plasmid that produced 2.7 mM.
靛蓝染料是一种具有独特蓝色的有机化合物。目前工业上使用的大多数靛蓝是通过化学合成生产的,这会产生大量废水。因此,最近进行了几项研究,以寻找利用微生物生态友好地生产靛蓝的方法。在这里,我们使用携带靛蓝生产质粒和环丙烷脂肪酸(CFA)调节质粒的重组大肠杆菌生产靛蓝。CFA调节质粒包含cfa基因,其表达会增加细胞膜磷脂脂肪酸的CFA组成。cfa的过表达显示出对靛蓝生产过程中形成的中间产物吲哚的细胞毒性抗性。这对靛蓝生产有积极影响,并且使用了源自假单胞菌属B 14 - 6的cfa。通过调整表达菌株、培养温度、振荡速度和异丙基β - D - 1 -硫代半乳糖苷浓度来确定靛蓝生产的最佳条件。用特定浓度的吐温80处理以增加细胞膜的通透性对靛蓝生产有积极影响。携带CFA质粒的菌株在培养24小时后产生了4.1 mM的靛蓝,比不携带CFA质粒的对照菌株产生的2.7 mM靛蓝高出1.5倍。