Literature DB >> 7765709

Antitumor activities and immunochemical properties of the cell-wall polysaccharides from Aureobasidium pullulans.

N Kataoka-Shirasugi1, J Ikuta, A Kuroshima, A Misaki.   

Abstract

Delipidated cell walls from Aureobasidium pullulans were fractionated systematically. The cell surface heteropolysaccharide contains D-mannose, D-galactose, D-glucose, and D-glucuronic acid (ratio, 8.5:3.9:1.0:1.0). It consists of a backbone of (1-->6)-alpha-linked D-mannose residues, some of which are substituted at 0-3 with single or beta-(1-->6)-linked D-galactofuranosyl side chains, some terminated with a D-glucuronic acid residue, and also with single residues of D-glucopyranose, D-galactopyranose, and D-mannopyranose. This glucurono-gluco-galactomannan interacted with antiserum against Elsinoe leucospila, which also reacted with its galactomannan, indicating that both polysaccharides contain a common epitope, i.e., at least terminal beta-galactofuranosyl groups and also possibly internal beta-(1-->6)-linked galactofuranose residues. It was further separated by DEAE-Sephacel column chromatography to gluco-galactomannan and glucurono-gluco-galactomannan. The alkali-extracted beta-D-glucan was purified by DEAE-cellulose chromatography to afford two antitumor-active (1-->3)-beta-D-glucans. One of the glucans (M(r), 1-2 x 10(5)) was a O-6-branched (1-->3)-beta-D-glucan with a single beta-D-glucosyl residue, d.b., 1/7, and the other (M(r), 3.5-4.5 x 10(5)) had similar branched structure, but having d.b., 1/5. Side chains of both glucans contain small proportions of beta-(1-->6)- and beta-(1-->4)-D-glucosidic linkages.

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Year:  1994        PMID: 7765709     DOI: 10.1271/bbb.58.2145

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  5 in total

1.  A small scale study on the effects of oral administration of the β-glucan produced by Aureobasidium pullulans on milk quality and cytokine expressions of Holstein cows, and on bacterial flora in the intestines of Japanese black calves.

Authors:  Hirofumi Uchiyama; Atsushi Iwai; Yukoh Asada; Daisuke Muramatsu; Shiho Aoki; Koji Kawata; Kisato Kusano; Koji Nagashima; Daisuke Yasokawa; Mitsuyasu Okabe; Tadaaki Miyazaki
Journal:  BMC Res Notes       Date:  2012-06-19

2.  Stimulation of macrophages with the β-glucan produced by aureobasidium pullulans promotes the secretion of tumor necrosis factor-related apoptosis inducing ligand (TRAIL).

Authors:  Koji Kawata; Atsushi Iwai; Daisuke Muramatsu; Shiho Aoki; Hirofumi Uchiyama; Mitsuyasu Okabe; Sumio Hayakawa; Akinori Takaoka; Tadaaki Miyazaki
Journal:  PLoS One       Date:  2015-04-13       Impact factor: 3.240

3.  Oral administration of the Aureobasidium pullulans-derived β-glucan effectively prevents the development of high fat diet-induced fatty liver in mice.

Authors:  Shiho Aoki; Atsushi Iwai; Koji Kawata; Daisuke Muramatsu; Hirofumi Uchiyama; Mitsuyasu Okabe; Masahiro Ikesue; Naoyoshi Maeda; Toshimitsu Uede
Journal:  Sci Rep       Date:  2015-07-16       Impact factor: 4.379

4.  Aureobasidium pullulans produced β-glucan is effective to enhance Kurosengoku soybean extract induced Thrombospondin-1 expression.

Authors:  Daisuke Muramatsu; Mitsuyasu Okabe; Akinori Takaoka; Hiroshi Kida; Atsushi Iwai
Journal:  Sci Rep       Date:  2017-06-06       Impact factor: 4.379

5.  β-Glucan derived from Aureobasidium pullulans is effective for the prevention of influenza in mice.

Authors:  Daisuke Muramatsu; Atsushi Iwai; Shiho Aoki; Hirohumi Uchiyama; Koji Kawata; Yosuke Nakayama; Yasuhiro Nikawa; Kisato Kusano; Mitsuyasu Okabe; Tadaaki Miyazaki
Journal:  PLoS One       Date:  2012-07-23       Impact factor: 3.240

  5 in total

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