4.4 Article

Cloning and characterization of β-agarase AgaYT from Flammeovirga yaeyamensis strain YT

期刊

JOURNAL OF BIOSCIENCE AND BIOENGINEERING
卷 112, 期 3, 页码 225-232

出版社

SOC BIOSCIENCE BIOENGINEERING JAPAN
DOI: 10.1016/j.jbiosc.2011.05.016

关键词

Flammeovirga yaeyamensis; Agarase; Thin-layer chromatography; Glycosyl hydrolase catalytic module; Degenerate primer

资金

  1. National Science Council of Taiwan [97-2622-B-017-001-CC1]
  2. Ministry of Education of Taiwan [98D1024]

向作者/读者索取更多资源

A bacterium with potent agar-degrading capability was isolated from the surface of a red algae, Gracilaria tenuistipitata. Based on phenotypic characteristics, 16S rDNA gene sequence and a phylogenetic analysis, this bacterium was identified and named as Flammeovirga yaeyamensis strain YT. PCR using homology-based degenerate primers was employed to clone any agarase gene belonging to GH16 family encoded in F. yaeyamensis strain YT. The resolved 1512 nucleotides revealed that the cloned gene, namely AgaYT, encodes a protein of 503 amino acids comprising a signal peptide, a glycosyl hydrolase catalytic module and a C-terminal domain with an unknown function. The recombinant protein r-AgaYT is an endo-type beta-agarase hydrolyzing agarose to yield neoagarobiose and neoagarotetraose as the main hydrolytic products. The specific activity of r-AgaYT was determined about 178.6 U mg(-1) at 40 degrees C and pH 8.0. (C) 2011, The Society for Biotechnology, Japan. All rights reserved.

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