Literature DB >> 34286020

Laminarin Quantification in Microalgae with Enzymes from Marine Microbes.

Stefan Becker1,2, Jan-Hendrik Hehemann1,2.   

Abstract

The marine beta-glucan laminarin is an abundant storage polysaccharide in microalgae. High production rates and rapid digestion by heterotrophic bacteria turn laminarin into an ideal carbon and energy source, and it is therefore a key player in the marine carbon cycle. As a main storage glucan laminarin also plays a central role in the energy metabolism of the microalgae (Percival and Ross, 1951; Myklestad, 1974; Painter, 1983). We take advantage of enzymes that digest laminarin selectively and can thereby quantify only this polysaccharide in environmental samples. These enzymes hydrolyze laminarin into glucose and oligosaccharides, which are measured with a standard reducing sugar assay to obtain the laminarin concentration. Prior to this assay, the three enzymes need to be produced via heterologous expression and purification. The assay can be used to monitor laminarin concentrations in environmental microalgae, which were concentrated from seawater by filtering, or in samples derived from algal lab cultures.
Copyright © 2017 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Algae; Chrysolaminarin; Diatoms; Glycobiology; Glycoside hydrolase; Laminarin; Laminarinase; Marine organic matter; β-Glucan

Year:  2018        PMID: 34286020      PMCID: PMC8275226          DOI: 10.21769/BioProtoc.2666

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  3 in total

1.  Accurate Quantification of Laminarin in Marine Organic Matter with Enzymes from Marine Microbes.

Authors:  Stefan Becker; André Scheffel; Martin F Polz; Jan-Hendrik Hehemann
Journal:  Appl Environ Microbiol       Date:  2017-04-17       Impact factor: 4.792

2.  A new reaction for colorimetric determination of carbohydrates.

Authors:  M Lever
Journal:  Anal Biochem       Date:  1972-05       Impact factor: 3.365

3.  Protein production by auto-induction in high density shaking cultures.

Authors:  F William Studier
Journal:  Protein Expr Purif       Date:  2005-05       Impact factor: 1.650

  3 in total

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