Characterization of a novel antibacterial N-acyl amino acid synthase from soil metagenome

• Published in: Journal of biotechnology Vol. 294; pp. 19 - 25
• Main Authors: Lee, Chang-Muk, Kim, Su-Yeon, Yoon, Sang-Hong, Kim, Jung-Bong, Yeo, Yoon-Soo, Sim, Joon-Soo, Hahn, Bum-Soo, Kim, Dong-Gwan
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 20.03.2019
• Subjects: Antibacterial agent; Lipoamino acid; Metagenome; N-acyl amino acid synthase; Lipoamino acid; Antibacterial agent; N-acyl amino acid synthase; Metagenome
• ISSN: 0168-1656; 1873-4863
• DOI: 10.1016/j.jbiotec.2019.01.017

•Finding N-acyl amino acid synthase (NAS) from soil metagenome clones.•Heterologous expression of the nasYPL gene conferred antibacterial activities.•nasYPL has antibacterial fractions identified N-acyl tyrosine, N-acyl phenylalanine, and N-acyl leucine.•Expression of nasYPL by host-specific manner may provide antibacterial characteristics. In an effort to isolate novel natural antibiotics, we searched for antibacterial long-chain N-acyl amino acid synthase (NAS) genes from 70,000 soil metagenome clones by Bacillus subtilis-overlaying screening. In an antibacterial cosmid clone, YS92B, a single gene nasYPL was responsible for the production of the Nas. nasYPL was 903 bp long, and the deduced amino acid sequence showed the highest 71% identity with a hypothetical protein from Massilia niastensis. Phylogenetic analysis demonstrated that NasYPL belongs to Group 1 Nas. Heterologous expression of the same nasYPL gene in Escherichia coli and two Pseudomonas strains (P. putida and P. koreensis) conferred antibacterial activities against Listeria monocytogenes, Staphylococcus epidermidis, and Bacillus subtilis. Mass spectral analysis of the antibacterial fractions identified 7 peaks corresponding to long-chain N-acyl tyrosine, 5 peaks to N-acyl phenylalanine, and 3 peaks to N-acyl leucine (or isoleucine) derivatives linked with 7 fatty acids, indicating enzymatic products derived by NasYPL. Therefore, NasYPL expression by host-specific manner may provide applicable antibacterial characteristics to biotechnologically important Pseudomonas strains.