High-Level Extracellular Production of a Trisaccharide-Producing Alginate Lyase AlyC7 in Escherichia coli and Its Agricultural Application

Author:

Wang Xiao-Han1234,Zhang Yu-Qiang1,Zhang Xin-Ru1,Zhang Xiao-Dong1,Sun Xiao-Meng2,Wang Xiao-Fei1,Sun Xiao-Hui1,Song Xiao-Yan13,Zhang Yu-Zhong123ORCID,Wang Ning13,Chen Xiu-Lan13ORCID,Xu Fei13ORCID

Affiliation:

1. State Key Laboratory of Microbial Technology, Marine Biotechnology Research Center, Shandong University, Qingdao 266237, China

2. Frontiers Science Center for Deep Ocean Multispheres and Earth System, College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China

3. Joint Research Center for Marine Microbial Science and Technology, Shandong University and Ocean University of China, Qingdao 266237, China

4. Shandong Key Laboratory of Marine Ecological Restoration, Shandong Marine Resource and Environment Research Institute, Yantai 264006, China

Abstract

Alginate oligosaccharides (AOS), products of alginate degradation by endotype alginate lyases, possess favorable biological activities and have broad applications. Although many have been reported, alginate lyases with homogeneous AOS products and secretory production by an engineered host are scarce. Herein, the alginate lyase AlyC7 from Vibrio sp. C42 was characterized as a trisaccharide-producing lyase exhibiting high activity and broad substrate specificity. With PelB as the signal peptide and 500 mM glycine as the additive, the extracellular production of AlyC7 in Escherichia coli reached 1122.8 U/mL after 27 h cultivation in Luria-Bertani medium. The yield of trisaccharides from sodium alginate degradation by the produced AlyC7 reached 758.6 mg/g, with a purity of 85.1%. The prepared AOS at 20 μg/mL increased the root length of lettuce, tomato, wheat, and maize by 27.5%, 25.7%, 9.7%, and 11.1%, respectively. This study establishes a robust foundation for the industrial and agricultural applications of AlyC7.

Funder

Marine S&T Fund of Shandong Province for Qingdao Marine Science and Technology Center

National Science Foundation of China

SKLMT Frontiers and Challenges Project

Publisher

MDPI AG

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