Skip to main content

Assaying Fucosidase Activity

  • Protocol
  • First Online:
  • 1711 Accesses

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1954))

Abstract

The characterization of a recombinant glycosidase can be done with commercially available substrates, which enable testing of enzyme functionality and determination of linkage specificity. Colorimetric assays with p-nitrophenyl substrates provide a relatively simple and fast way of screening conditions which could affect enzyme activity (buffer, pH, ion dependence, temperature). These substrates are useful for the determination of activity optima and the characterization of basic activity parameters. However, testing for linkage specificity should be performed on more complex sugars presenting a range of different glycosidic bonds and might need more sophisticated methods of analysis. This protocol provides comprehensive instructions on how to perform an initial characterization of your glycosidase using a recombinant α-l-fucosidase as an example.

This is a preview of subscription content, log in via an institution.

Buying options

Protocol
USD   49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD   219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Springer Nature is developing a new tool to find and evaluate Protocols. Learn more

References

  1. Megson ZA, Koerdt A, Schuster H et al (2015) Characterization of an α-L-fucosidase from the periodontal pathogen Tannerella forsythia. Virulence 6:282–292

    Article  CAS  Google Scholar 

  2. Guillotin L, Lafite P, Daniellou R (2014) Unraveling the substrate recognition mechanism and specificity of the unusual glycosyl hydrolase family 29 BT2192 from Bacteroides thetaiotaomicron. Biochemist 53:1447–1455

    Article  CAS  Google Scholar 

  3. Berteau O, McCort I, Goasdoue N et al (2002) Characterization of a new α-L-fucosidase isolated from the marine mollusk Pecten maximus that catalyzes the hydrolysis of α-L-fucose from algal fucoidan (Ascophyllum nodosum). Glycobiology 12:273–282

    Article  CAS  Google Scholar 

  4. Rodriguez-Diaz J, Monedero V, Yebra MJ (2011) Utilization of natural fucosylated oligosaccharides by three novel α-L-fucosidases from a probiotic Lactobacillus casei strain. Appl Environ Microbiol 77:703–705

    Article  CAS  Google Scholar 

  5. Leonard R, Rendic D, Rabouille C et al (2006) The Drosophila fused lobes gene encodes an N-acetylglucosaminidase involved in N-glycan processing. J Biol Chem 281:4867–4875

    Article  CAS  Google Scholar 

  6. McIlvaine TA (1921) A buffer solution for colorimetric comparison. J Biol Chem 49:183–186

    CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by the Austrian Science Fund FWF, projects P24317-B22 (to C.S.) and the Doctoral Programme W1224 Biomolecular Technology of Proteins.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Christina Schäffer .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Megson, Z.A., Messner, P., Schäffer, C. (2019). Assaying Fucosidase Activity. In: Brockhausen, I. (eds) Bacterial Polysaccharides. Methods in Molecular Biology, vol 1954. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-9154-9_21

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-9154-9_21

  • Published:

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-9153-2

  • Online ISBN: 978-1-4939-9154-9

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics