Zhenpeng Zhang, Chaoya Wu, Shuai Shao, Wei Liu, En-Tao Wang, Yan Li. Diversity of protease-producing bacteria in the Bohai Bay sediment and their extracellular enzymatic properties[J]. Acta Oceanologica Sinica. doi: 10.1007/s13131-020-1589-x
Citation:
Zhenpeng Zhang, Chaoya Wu, Shuai Shao, Wei Liu, En-Tao Wang, Yan Li. Diversity of protease-producing bacteria in the Bohai Bay sediment and their extracellular enzymatic properties[J]. Acta Oceanologica Sinica. doi: 10.1007/s13131-020-1589-x
Zhenpeng Zhang, Chaoya Wu, Shuai Shao, Wei Liu, En-Tao Wang, Yan Li. Diversity of protease-producing bacteria in the Bohai Bay sediment and their extracellular enzymatic properties[J]. Acta Oceanologica Sinica. doi: 10.1007/s13131-020-1589-x
Citation:
Zhenpeng Zhang, Chaoya Wu, Shuai Shao, Wei Liu, En-Tao Wang, Yan Li. Diversity of protease-producing bacteria in the Bohai Bay sediment and their extracellular enzymatic properties[J]. Acta Oceanologica Sinica. doi: 10.1007/s13131-020-1589-x
Key Laboratory of Coastal Biology and Utilization, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China
2.
Life Science College, Yantai University, Yantai 264005, China
3.
Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Mexico City D.F. 11340, México
4.
University of Chinese Academy of Sciences (UCAS), Beijing 100049, China
Funds:
The National Natural Science Foundation of China under contract Nos 31600009 and 31800099; the Key Research and Development Program of Hebei Province under contract No. 19273802D; the STS Program of Chinese Academy of Sciences and Fujian Province under contract No. 2017T3019; the Yantai Science and Technology Project under contract No. 2018ZHGY074; the Joint Fund of Jilin Province and Chinese Academy of Sciences for High-tech Industrialization under contract No. 2019SYHZ0036; En-Tao Wang was supported by the projects under contract Nos SIP 20150597 and 20160883 authorized by IPN, Mexico.
Protease-producing bacteria play key roles in the degradation of organic nitrogen materials in marine sediments. However, their diversity, production of proteases and other extracellular enzymes, even in situ ecological functions remain largely unknown. In this study, we investigated the diversity of cultivable extracellular protease-producing bacteria in the sediments of the Bohai Bay. A total of 109 bacterial isolates were obtained from the sediments of 7 stations. The abundance of cultivable protease-producing bacteria was about 104 CFU/g of sediment in all the samples. Phylogenetic analysis based on 16S rRNA gene sequences classified all the isolates into 14 genera from phyla Proteobacteria, Firmicutes, Bacteroidetes and Actinobacteria, with Pseudoalteromonas (63/109, 57.8%), Bacillus (9/109, 8.2%), Sulfitobacter (8/109, 7.3%) and Salegentibacter (6/109, 5.5%) as the dominant taxa. Enzymatic inhibition tests indicated that all the tested isolates produced serine and/or metalloprotease, with only a small proportion producing cysteine and/or aspartic proteases. Several extracellular enzyme activities, including alginase, lipase, amylase and cellulose, and nitrate reduction were also detected for strains with higher protease activities. According the results, the protease-producing bacteria could also be participate in many biogeochemical processes in marine sediments. Our study broadened understanding and knowledge on the potential ecological functions of protease-producing bacteria in marine sediments.
Figure 1. Map of the Bohai Bay in the Bohai Sea of China showing the sampling sites (●). The map was created using DIVA-GIS software (http//www.diva-gis.org), and the sampling sites were added according to GPS records.
Figure 2. Phylogenetic tree of the protease-producing bacteria isolated from the Bohai Bay based on 16S rRNA gene sequences. Taxa and GenBank accession numbers in boldface were generated in this study. The tree was constructed by neighbor-joining method using MEGA version 6.0. Only bootstrap values greater than 50% are presented in the nodes. The scale bar represents 2% nucleotide substitution.