4.6 Article

Specificities and Synergistic Actions of Novel PL8 and PL7 Alginate Lyases from the Marine Fungus Paradendryphiella salina

期刊

JOURNAL OF FUNGI
卷 7, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/jof7020080

关键词

alginate lyase; polysaccharide lyase; marine fungi; enzyme characterization; alginate; polymannuronic acid; polyguluronic acid; exo-acting

资金

  1. European Commission H2020 Bio-based Industries Joint Consortium via the Macro Cascade Project, BBI Grant [720755]
  2. MARIKAT JPI Cofund Blue BioEconomy Project [9082-00021B]
  3. Technical University of Denmark

向作者/读者索取更多资源

Alginate is an anionic polysaccharide found in brown macroalgae, with enzymatic depolymerization mainly carried out by alginate lyases. A marine fungus, Paradendryphiella salina, was found to have four alginate lyases, including one PL8 and three PL7 enzymes. These enzymes showed different substrate specificities and activities in the depolymerization of alginate and polymannuronic acid.
Alginate is an anionic polysaccharide abundantly present in the cell walls of brown macroalgae. The enzymatic depolymerization is performed solely by alginate lyases (EC 4.2.2.x), categorized as polysaccharide lyases (PLs) belonging to 12 different PL families. Until now, the vast majority of the alginate lyases have been found in bacteria. We report here the first extensive characterization of four alginate lyases from a marine fungus, the ascomycete Paradendryphiella salina, a known saprophyte of seaweeds. We have identified four polysaccharide lyase encoding genes bioinformatically in P. salina, one PL8 (PsMan8A), and three PL7 alginate lyases (PsAlg7A, -B, and -C). PsMan8A was demonstrated to exert exo-action on polymannuronic acid, and no action on alginate, indicating that this enzyme is most likely an exo-acting polymannuronic acid specific lyase. This enzyme is the first alginate lyase assigned to PL8 and polymannuronic acid thus represents a new substrate specificity in this family. The PL7 lyases (PsAlg7A, -B, and -C) were found to be endo-acting alginate lyases with different activity optima, substrate affinities, and product profiles. PsAlg7A and PsMan8A showed a clear synergistic action for the complete depolymerization of polyM at pH 5. PsAlg7A depolymerized polyM to mainly DP5 and DP3 oligomers and PsMan8A to dimers and monosaccharides. PsAlg7B and PsAlg7C showed substrate affinities towards both polyM and polyG at pH 8, depolymerizing both substrates to DP9-DP2 oligomers. The findings elucidate how P. salina accomplishes alginate depolymerization and provide insight into an efficient synergistic cooperation that may provide a new foundation for enzyme selection for alginate degradation in seaweed bioprocessing.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据