Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Mar 21:5:100022.
doi: 10.1016/j.tcsw.2019.100022. eCollection 2019 Dec.

Cell wall glucans of fungi. A review

Affiliations
Review

Cell wall glucans of fungi. A review

José Ruiz-Herrera et al. Cell Surf. .

Abstract

Glucans are the most abundant polysaccharides in the cell walls of fungi, and their structures are highly variable. Accordingly, their glucose moieties may be joined through either or both alpha (α) or beta (β) linkages, they are either lineal or branched, and amorphous or microfibrillar. Alpha 1,3 glucans sensu strictu (pseudonigerans) are the most abundant alpha glucans present in the cell walls of fungi, being restricted to dikarya. They exist in the form of structural microfibrils that provide resistance to the cell wall. The structure of beta glucans is more complex. They are linear or branched, and contain mostly β 1,3 and β 1,6 linkages, existing in the form of microfibrils. Together with chitin they constitute the most important structural components of fungal cell walls. They are the most abundant components of the cell walls in members of all fungal phyla, with the exception of Microsporidia, where they are absent. Taking into consideration the importance of glucans in the structure and physiology of the fungi, in the present review we describe the following aspects of these polysaccharides: i) types and distribution of fungal glucans, ii) their structure, iii) their roles, iv) the mechanism of synthesis of the most important ones, and v) the phylogentic relationships of the enzymes involved in their synthesis.

Keywords: Alpha glucans; Beta glucans; Cell wall; Fungi; Phylogenetic analyses.

PubMed Disclaimer

Figures

None
Graphical abstract
Fig. 1
Fig. 1
Evolutionary relationships of alpha glucan synthases from the Basidiomycota subphyla in relation to the enzymes from Ascomycota. The MEGA6 program (Tamura et al., 2013) was used to obtain the dendrogram generated by the Maximum Likelihood method based on the Le Gascuel 2008 model (Le and Gascuel, 1993), with 1000 bootstraps (Felsenstein, 1985). The percentage of trees in which the associated taxa clustered together is shown next to the branches. Initial tree(s) for the heuristic search were obtained by applying the Neighbor-Joining method to a matrix of pairwise distances estimated using a JTT model. A discrete Gamma distribution was used to model evolutionary rate differences among sites [5 categories (+G, parameter = 0.8908]. Evolutionary analyses were conducted in MEGA6 (Tamura et al., 2013). BASIDIO, Basidiomycota; ASCO, Ascomycota; Agarico, Agaricomycotina; Puccinio, Pucciniomycotina; Ustilagino, Ustilaginomycotina. Beta GS, rooting group of β-1,3 glucan synthases.
Fig. 2
Fig. 2
Phylogenetic tree showing the relationships of the identified fungal α 1,3 glucan synthases. Analysis was made of 309 sequences as described for Fig. 1, with 100 bootstraps. Letters refer to orders of Basidiomycota: A, Agaricales, Polyporales, Gloeophyllales, Jaapiales, Russulales, Amylocorticiales, Sebacinales, and Geastrales, B, Cantharellales, C, Tremellales, D, Pucciniales and Spiculogloeales, and E, Exobasidiales. Numbers refer to orders of Ascomycota: 1, Schizosaccharomycetales, Taphrinales, and Neolectales, 2, Dothideales, 3, Eurotiales, 4. Sordariales and Botryosphaeriales, 5, Capnodiales, 6, Glomerellales, Xylariales, Diaporthales, Coniochaetales, Pleosporales, Hypocreales and Magnaporthales, 7, Helotiales, 8. Chaetothyriales, 9, Verrucariales and Phaeomoniellales, and 10, Onygenales. Beta GS, β 1, 3 glucan synthases rooting group. Letters and numbers correspond to the fungal orders involving the species described in Table 1, that were used to construct the tree.
Fig. 3
Fig. 3
Phylogenetic tree showing the relationships of identified fungal β 1, 3 glucan synthases. Analysis of 500 sequences was made as described for Fig. 1, with 100 bootstraps. Lower case letter a refers to Chitridiomycota of the order Blastocladiales. Capital letters refer to orders of Mucoromycota: A, Mucorales, B, Entomophthorales, Kickxellales, and Harpellales, C, Basidiobolales and Mortierellales. Roman numerals refer to orders of Basidiomycota: I, Agaricales, Boletales, Corticiales, Polyporales, Russulales, Gloeophyllales, Jaapiales, Hymenochaetaleas, Sebacinales, Cantharellales, Dacrymycetales, Geastrales, Auriculariales, Amylocorticiales, Tremellales, Trichosporonales, and Wallemiales, II, Pucciniales, Mixiales, Microbotryales, Leucosporidiales, and Sporidiobolales, III, Ustilaginales, Ceraceosorales, and Malasseziales. Arabic numerals refer to orders of Ascomycota, 1, Saccharomycetales, 2, Schizosaccharomycetales, 3, Taphrinales, Neolectales, Pneumocystidales, Pezizales, and Orbiliales, 4, Hypocreales, Microascales, Glomerellales, Magnaporthales, Diaporthales, Ophiostomatales, Sordariales, Xylariales, and Togniniales, 5, Helotiales, and Erysiphales, 6, Eurotiales, 7, Onygenales, 8, Chaetothyriomycetales, Umbilicariales, Verrucariales, 9, Capnodiales, Dothideales, Venturiales, Botryosphaeriales, and Pleosporales. alpha GS, α 1, 3 glucan syntases rooting group. Letters and numbers correspond to the fungal orders involving the species described in Table 2, that were used to construct the tree.

References

    1. Almanianda V., Simenel C., Garnaud C. The dual activity responsible for the elongation and branching of β-(1,3)-Glucan in the fungal cell wall. mBio. 2017;8:e00619–e717. - PMC - PubMed
    1. Andaluz E., Guilen A., Larriba G. Preliminary evidence for a glucan acceptor in the yeast Saccharomyces cerevisiae. Biochem. J. 1986;240:495–502. - PMC - PubMed
    1. Andaluz E., Ridruejo C.C., Ramirez M. Initiation of glucan synthesis in yeast. FEMS Microbiol. Let. 1988;49:251–255.
    1. Aronson J.M., Machlis L. The chemical composition of the hyphal walls of the fungus Allomyces. Amer. J. Bot. 1959;46:292–300.
    1. Bacon J.S.D., Jones D., Farmer V.C. The occurrence of (13)-α-glucan in Cryptococcus, Schizosaccharomyces and Polyporus species, and its hydrolysis by a Streptomyces culture filtrate lysing cell walls of Cryptococcus. BBA. 1968;158:313–315. - PubMed

LinkOut - more resources