Exploring regulation genes involved in the expression of L-amino acid oxidase in Pseudoalteromonas sp. Rf-1

PLoS One. 2015 Mar 27;10(3):e0122741. doi: 10.1371/journal.pone.0122741. eCollection 2015.

Abstract

Bacterial L-amino acid oxidase (LAAO) is believed to play important biological and ecological roles in marine niches, thus attracting increasing attention to understand the regulation mechanisms underlying its production. In this study, we investigated genes involved in LAAO production in marine bacterium Pseudoalteromonas sp. Rf-1 using transposon mutagenesis. Of more than 4,000 mutants screened, 15 mutants showed significant changes in LAAO activity. Desired transposon insertion was confirmed in 12 mutants, in which disrupted genes and corresponding functionswere identified. Analysis of LAAO activity and lao gene expression revealed that GntR family transcriptional regulator, methylase, non-ribosomal peptide synthetase, TonB-dependent heme-receptor family, Na+/H+ antiporter and related arsenite permease, N-acetyltransferase GCN5, Ketol-acid reductoisomerase and SAM-dependent methytransferase, and their coding genes may be involved in either upregulation or downregulation pathway at transcriptional, posttranscriptional, translational and/or posttranslational level. The nhaD and sdmT genes were separately complemented into the corresponding mutants with abolished LAAO-activity. The complementation of either gene can restore LAAO activity and lao gene expression, demonstrating their regulatory role in LAAO biosynthesis. This study provides, for the first time, insights into the molecular mechanisms regulating LAAO production in Pseudoalteromonas sp. Rf-1, which is important to better understand biological and ecological roles of LAAO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / biosynthesis*
  • Bacterial Proteins / genetics
  • Gene Expression Regulation, Enzymologic*
  • L-Amino Acid Oxidase / genetics*
  • L-Amino Acid Oxidase / metabolism
  • Mutagenesis
  • Pseudoalteromonas / enzymology*

Substances

  • Bacterial Proteins
  • L-Amino Acid Oxidase

Grants and funding

This work was supported by Regional Demonstration of Marine Economy Innovative Development Project, China (No. 12PYY001SF08) (http://www.soa.gov.cn/), Natural Science Foundation of Zhejiang Province, China (No. Y5100153) (http://www.zjnsf.gov.cn/index.aspx) and Graduate Students’ Science and Technology Innovation Program (Youth Talent Plan) of Zhejiang Province, China (No. 2014R403103) (http://www.zjkjt.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.