Literature DB >> 19866663

SYNTHESIS OF CELLULOSE BY ACETOBACTER XYLINUM: VIII. On the Formation and Orientation of Bacterial Cellulose Fibrils in the Presence of Acidic Polysaccharides.

G Ben-Hayyim1, I Ohad.   

Abstract

The transfer of the glucosyl moiety from uridine diphosphate glucose in the presence of Acetobacter xylinum cell-free extracts led to the formation of a mixture of alkali-soluble and -insoluble cellodextrins. Typical cellulose fibrils could not be detected by electron microscopy in this product. Immediately after release into the medium, cellulose formed by whole cells is in a "prefibrous" form which passes through Millipore filters of 0.45 and 0.8 micro pore diameter. Non-filtrable fibrils arise from this material probably by a process of crystallization involving no extracellular enzymes. Fibrils formed in shaken cell suspensions intertwine and form aggregates visible to the naked eye. In quiet suspensions pellicles are formed which float on the surface. Soluble Na-carboxymethylcellulose (CMC) is incorporated into cellulose fibrils formed in its presence, probably by a process of co-crystallization. Aggregation of fibrils containing CMC is delayed because of electrostatic repulsion between carboxylic groups. The aggregation time depends on the amount of CMC incorporated, its degree of substitution, the pH of the medium, and the ionic strength. The amount of CMC incorporated depends on the relative concentration CMC/cellulose and on the similarity of the CMC and the cellulose molecules i.e. in molecular weight and the number of carboxyl substitutions. Cellulose pellicles formed in the presence of CMC by unshaken cell suspensions consist of crossed, superimposed layers of parallel oriented cellulose fibrils. The same phenomenon is observed when phosphomannan, but not levan, is substituted for CMC. The biogenesis of oriented cellulose fibrils is envisaged as a process comprising the following steps: polymerization of the monomeric precursor, diffusion of the molecule to crystallization sites, crystallization, and orientation. It is proposed that charged polysaccharides play a role similar to that of CMC in affecting the orientation of cellulose fibrils in the plant cell wall.

Entities:  

Year:  1965        PMID: 19866663      PMCID: PMC2106645          DOI: 10.1083/jcb.25.2.191

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  15 in total

1.  Oriented cellulose as a component of mammalian tissue.

Authors:  D A HALL; F HAPPEY; P F LLOYD; H SAXL
Journal:  Proc R Soc Lond B Biol Sci       Date:  1960-03-01

2.  The formation of cellulose microfibrils in suspensions of Acetobacter xylinum.

Authors:  J R COLVIN; M BEER
Journal:  Can J Microbiol       Date:  1960-12       Impact factor: 2.419

3.  Concerning the role of wall stresses in the elongation of the Nitella cell.

Authors:  P B GREEN; J C CHEN
Journal:  Z Wiss Mikrosk       Date:  1960-11

4.  The formation of cellulose microfibrils by Acetobacter xylinum in agar surfaces.

Authors:  B MILLMAN; J R COLVIN
Journal:  Can J Microbiol       Date:  1961-06       Impact factor: 2.419

5.  Synthesis of bacterial cellulose from labeled precursor.

Authors:  A W KHAN; J R COLVIN
Journal:  Science       Date:  1961-06-23       Impact factor: 47.728

6.  Synthesis of cellulose by Acetobacter Xylinum. 3. Substrates and inhibitors.

Authors:  M SCHRAMM; Z GROMET; S HESTRIN
Journal:  Biochem J       Date:  1957-12       Impact factor: 3.857

7.  The synthesis of cellulose in cell-free extracts of Acetobacter xylinum.

Authors:  L GLASER
Journal:  J Biol Chem       Date:  1958-06       Impact factor: 5.157

8.  Deposition of wall material in thickened primary walls of elongating plant cells.

Authors:  G SETTERFIELD; S T BAYLEY
Journal:  Exp Cell Res       Date:  1958-06       Impact factor: 3.905

9.  ON THE DIMENSIONS OF CELLULOSE MICROFIBRILS.

Authors:  I OHAD; D DANON
Journal:  J Cell Biol       Date:  1964-07       Impact factor: 10.539

10.  Synthesis of cellulose by Acetobacter xylinum. V. Ultrastructure of polymer.

Authors:  I OHAD; I O DANON; S HESTRIN
Journal:  J Cell Biol       Date:  1962-01       Impact factor: 10.539

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  5 in total

1.  Structure and association of wall fibrils produced by regenerating tobacco protoplasts.

Authors:  J Burgess; P J Linstead
Journal:  Planta       Date:  1979-01       Impact factor: 4.116

2.  Further characterization of the alkali-stable material from the scales of Pleurochrysis scherffelii: A cellulosic glycoprotein.

Authors:  W Herth; W W Franke; J Stadler; H Bittiger; G Keilich; R M Brown
Journal:  Planta       Date:  1972-03       Impact factor: 4.116

3.  Time relationships of sporopollenin synthesis associated with tapetum and microspores in Lilium.

Authors:  J Heslop-Harrison; H G Dickinson
Journal:  Planta       Date:  1969-09       Impact factor: 4.116

4.  Isolation of alpha-glucan and lipopolysaccharide fractions from Acetobacter xylinum.

Authors:  R F Dekker; E T Rietschel; H Sandermann
Journal:  Arch Microbiol       Date:  1977-12-15       Impact factor: 2.552

Review 5.  Potential Applications of Nanocellulose-Containing Materials in the Biomedical Field.

Authors:  Nadia Halib; Francesca Perrone; Maja Cemazar; Barbara Dapas; Rossella Farra; Michela Abrami; Gianluca Chiarappa; Giancarlo Forte; Fabrizio Zanconati; Gabriele Pozzato; Luigi Murena; Nicola Fiotti; Romano Lapasin; Laura Cansolino; Gabriele Grassi; Mario Grassi
Journal:  Materials (Basel)       Date:  2017-08-21       Impact factor: 3.623

  5 in total

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