Cargando…

Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis

Background: Alginate lyases belonging to polysaccharide lyase family-7 (PL-7) are the most well studied on their structures and functions among whole alginate lyases. However, all characterized PL-7 alginate lyases are from prokaryotic bacteria cells. Here we report the first identification of eukar...

Descripción completa

Detalles Bibliográficos
Autores principales: Inoue, Akira, Mashino, Chieco, Uji, Toshiki, Saga, Naotsune, Mikami, Koji, Ojima, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436490/
https://www.ncbi.nlm.nih.gov/pubmed/28553576
http://dx.doi.org/10.2174/2211550104666150915210434
_version_ 1783237415744307200
author Inoue, Akira
Mashino, Chieco
Uji, Toshiki
Saga, Naotsune
Mikami, Koji
Ojima, Takao
author_facet Inoue, Akira
Mashino, Chieco
Uji, Toshiki
Saga, Naotsune
Mikami, Koji
Ojima, Takao
author_sort Inoue, Akira
collection PubMed
description Background: Alginate lyases belonging to polysaccharide lyase family-7 (PL-7) are the most well studied on their structures and functions among whole alginate lyases. However, all characterized PL-7 alginate lyases are from prokaryotic bacteria cells. Here we report the first identification of eukaryotic PL-7 alginate lyase from marine red alga Pyropia yezoensis. Methods: The cDNA encoding an alginate lyase PyAly was cloned and was used for the construction of recombinant PyAly (rPyAly) expression system in Escherichia coli. Purified rPyAly was assayed to identify its enzymatic properties. Its expression pattern in P. yessoensis was also investigated. Results: PyAly is likely a secreted protein consisting of an N-terminal signal peptide of 25 residues and a catalytic domain of 216 residues. The amino-acid sequence of the catalytic domain showed 19-29% identities to those of bacterial characterized alginate lyases classified into family PL-7. Recombinant PyAly protein, rPyAly, which was produced with E. coli BL21(DE3) by cold-inducible expression system, drastically decreased the viscosity of alginate solution in the early stage of reaction. The most preferable substrate for rPyAly was the poly(M) of alginate with an optimal temperature and pH at 35(o)C and 8.0, respectively. After reaction, unsaturated tri- and tetra-saccharides were produced from poly(M) as major end products. These enzymatic properties indicated that PyAly is an endolytic alginate lyase belonging to PL-7. Moreover, we found that the PyAly gene is split into 4 exons with 3 introns. PyAly was also specifically expressed in the gametophytic haplopid stage. Conclusion: This study demonstrates that PyAly in marine red alga P. yezoensis is a novel PL-7 alginate lyase with an endolytic manner. PyAly is a gametophyte-specifically expressed protein and its structural gene is composed of four exons and three introns. Thus, PyAly is the first enzymatically characterized eukaryotic PL-7 alginate lyase.
format Online
Article
Text
id pubmed-5436490
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Bentham Science Publishers
record_format MEDLINE/PubMed
spelling pubmed-54364902017-05-26 Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis Inoue, Akira Mashino, Chieco Uji, Toshiki Saga, Naotsune Mikami, Koji Ojima, Takao Curr Biotechnol Article Background: Alginate lyases belonging to polysaccharide lyase family-7 (PL-7) are the most well studied on their structures and functions among whole alginate lyases. However, all characterized PL-7 alginate lyases are from prokaryotic bacteria cells. Here we report the first identification of eukaryotic PL-7 alginate lyase from marine red alga Pyropia yezoensis. Methods: The cDNA encoding an alginate lyase PyAly was cloned and was used for the construction of recombinant PyAly (rPyAly) expression system in Escherichia coli. Purified rPyAly was assayed to identify its enzymatic properties. Its expression pattern in P. yessoensis was also investigated. Results: PyAly is likely a secreted protein consisting of an N-terminal signal peptide of 25 residues and a catalytic domain of 216 residues. The amino-acid sequence of the catalytic domain showed 19-29% identities to those of bacterial characterized alginate lyases classified into family PL-7. Recombinant PyAly protein, rPyAly, which was produced with E. coli BL21(DE3) by cold-inducible expression system, drastically decreased the viscosity of alginate solution in the early stage of reaction. The most preferable substrate for rPyAly was the poly(M) of alginate with an optimal temperature and pH at 35(o)C and 8.0, respectively. After reaction, unsaturated tri- and tetra-saccharides were produced from poly(M) as major end products. These enzymatic properties indicated that PyAly is an endolytic alginate lyase belonging to PL-7. Moreover, we found that the PyAly gene is split into 4 exons with 3 introns. PyAly was also specifically expressed in the gametophytic haplopid stage. Conclusion: This study demonstrates that PyAly in marine red alga P. yezoensis is a novel PL-7 alginate lyase with an endolytic manner. PyAly is a gametophyte-specifically expressed protein and its structural gene is composed of four exons and three introns. Thus, PyAly is the first enzymatically characterized eukaryotic PL-7 alginate lyase. Bentham Science Publishers 2015-08 2015-08 /pmc/articles/PMC5436490/ /pubmed/28553576 http://dx.doi.org/10.2174/2211550104666150915210434 Text en © 2015 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Inoue, Akira
Mashino, Chieco
Uji, Toshiki
Saga, Naotsune
Mikami, Koji
Ojima, Takao
Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title_full Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title_fullStr Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title_full_unstemmed Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title_short Characterization of an Eukaryotic PL-7 Alginate Lyase in the Marine Red Alga Pyropia yezoensis
title_sort characterization of an eukaryotic pl-7 alginate lyase in the marine red alga pyropia yezoensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436490/
https://www.ncbi.nlm.nih.gov/pubmed/28553576
http://dx.doi.org/10.2174/2211550104666150915210434
work_keys_str_mv AT inoueakira characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis
AT mashinochieco characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis
AT ujitoshiki characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis
AT saganaotsune characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis
AT mikamikoji characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis
AT ojimatakao characterizationofaneukaryoticpl7alginatelyaseinthemarineredalgapyropiayezoensis