Literature DB >> 22311108

Determination of cellulase colocalization on cellulose fiber with quantitative FRET measured by acceptor photobleaching and spectrally unmixing fluorescence microscopy.

Liqun Wang1, Yiqing Wang, Arthur J Ragauskas.   

Abstract

The determination of cellulase distribution on the surface of cellulose fiber is an important parameter to understand when determining the interaction between cellulase and cellulose and/or the cooperation of different types of cellulases during the enzymatic hydrolysis of cellulose. In this communication, a strategy is presented to quantitatively determine the cellulase colocalization using the fluorescence resonance energy transfer (FRET) methodology, which is based on acceptor photobleaching and spectrally unmixing fluorescence microscopy. FRET monitoring of cellulase colocalization was achieved by labeling cellulases with an appropriate pair of FRET dyes and by adopting an appropriate FRET model. We describe here that the adapted acceptor photobleaching FRET method can be successfully used to quantify cellulase colocalization regarding their binding to a cellulose fiber at a resolution <10 nm. This developed quantitative FRET method is promising for further studying the interactions between cellulase and cellulose and between different types of cellulases.

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Year:  2012        PMID: 22311108     DOI: 10.1039/c2an15938d

Source DB:  PubMed          Journal:  Analyst        ISSN: 0003-2654            Impact factor:   4.616


  4 in total

1.  Visualising recalcitrance by colocalisation of cellulase, lignin and cellulose in pretreated pine biomass using fluorescence microscopy.

Authors:  Lloyd Donaldson; Alankar Vaidya
Journal:  Sci Rep       Date:  2017-03-10       Impact factor: 4.379

2.  FRET-SLiM on native autofluorescence: a fast and reliable method to study interactions between fluorescent probes and lignin in plant cell wall.

Authors:  Christine Terryn; Gabriel Paës; Corentin Spriet
Journal:  Plant Methods       Date:  2018-08-27       Impact factor: 4.993

3.  Dimerization of human uridine diphosphate glucuronosyltransferase allozymes 1A1 and 1A9 alters their quercetin glucuronidation activities.

Authors:  Yan-Qing Liu; Ling-Min Yuan; Zhang-Zhao Gao; Yong-Sheng Xiao; Hong-Ying Sun; Lu-Shan Yu; Su Zeng
Journal:  Sci Rep       Date:  2016-03-30       Impact factor: 4.379

Review 4.  Report on the Current Inventory of the Toolbox for Plant Cell Wall Analysis: Proteinaceous and Small Molecular Probes.

Authors:  Maja G Rydahl; Aleksander R Hansen; Stjepan K Kračun; Jozef Mravec
Journal:  Front Plant Sci       Date:  2018-05-03       Impact factor: 5.753

  4 in total

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