Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain
The structure of pullulan, the extracellular -D-glucan elaborated by the yeast-like fungus Aureobasidium pullulans, may be described as a linear -D-glucan consisting of maltotriosyl repeat units connected terminally by (1 6)- -D-glucosidic bonds. Occasionally some of maltotriosyl residues a...
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Serbian Chemical Society
2001-01-01
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doaj-bfbee271a1464996aaf44ad9270c48b62020-12-24T07:35:14ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51391820-74212001-01-0166637738310.2298/JSC0106377J0352-51390106377JFine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strainJakovljević Dragica0Vrvić Miroslav M.1Radulović Milanka2Hranisavljević-Jakovljević Mirjana3Institute of Chemistry, Technology and Metallurgy, Centre for Chemistry, BelgradeFaculty of Chemistry, BelgradeInstitute of Chemistry, Technology and Metallurgy, Centre for Chemistry, BelgradeFaculty of Chemistry, BelgradeThe structure of pullulan, the extracellular -D-glucan elaborated by the yeast-like fungus Aureobasidium pullulans, may be described as a linear -D-glucan consisting of maltotriosyl repeat units connected terminally by (1 6)- -D-glucosidic bonds. Occasionally some of maltotriosyl residues are replaced by higher oligosaccharide units, most frequently with maltotetraosyl residues. Using the susceptibility of pullulan CH-1 (obtained from strain CH-1 of Aureobasidium pullulans) to hydrolysis catalysed by porcine alpha-amylase, the polysaccharide was cleaved and the fragments obtained fractionated by gel-permeation chromatography. The heterogenous size of the fragments indicates that there is no apparent regular distribution of tetrasaccharide units in the pullulan chain. Enzymatic digestion of pullulan CH-1 using pullulanase, followed by gel-permeation chromatography of the resulting digest confirmed these results as did preparative paper chromatography and CI mass spectrometry of the separated components, i.e., that maltotetraosyl units (about 7%) are building units of pullulan CH-1.http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390106377J.pdfaureobasidium pullulanspolysaccharidepullulanamylolysispullulanolysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jakovljević Dragica Vrvić Miroslav M. Radulović Milanka Hranisavljević-Jakovljević Mirjana |
spellingShingle |
Jakovljević Dragica Vrvić Miroslav M. Radulović Milanka Hranisavljević-Jakovljević Mirjana Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain Journal of the Serbian Chemical Society aureobasidium pullulans polysaccharide pullulan amylolysis pullulanolysis |
author_facet |
Jakovljević Dragica Vrvić Miroslav M. Radulović Milanka Hranisavljević-Jakovljević Mirjana |
author_sort |
Jakovljević Dragica |
title |
Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain |
title_short |
Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain |
title_full |
Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain |
title_fullStr |
Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain |
title_full_unstemmed |
Fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, CH-1 strain |
title_sort |
fine structural analysis of the fungal polysaccharide pullulan elaborated by aureobasidium pullulans, ch-1 strain |
publisher |
Serbian Chemical Society |
series |
Journal of the Serbian Chemical Society |
issn |
0352-5139 1820-7421 |
publishDate |
2001-01-01 |
description |
The structure of pullulan, the extracellular -D-glucan elaborated by the
yeast-like fungus Aureobasidium pullulans, may be described as a linear
-D-glucan consisting of maltotriosyl repeat units connected terminally by
(1 6)- -D-glucosidic bonds. Occasionally some of maltotriosyl residues are
replaced by higher oligosaccharide units, most frequently with
maltotetraosyl residues. Using the susceptibility of pullulan CH-1 (obtained
from strain CH-1 of Aureobasidium pullulans) to hydrolysis catalysed by
porcine alpha-amylase, the polysaccharide was cleaved and the fragments
obtained fractionated by gel-permeation chromatography. The heterogenous
size of the fragments indicates that there is no apparent regular
distribution of tetrasaccharide units in the pullulan chain. Enzymatic
digestion of pullulan CH-1 using pullulanase, followed by gel-permeation
chromatography of the resulting digest confirmed these results as did
preparative paper chromatography and CI mass spectrometry of the separated
components, i.e., that maltotetraosyl units (about 7%) are building units
of pullulan CH-1. |
topic |
aureobasidium pullulans polysaccharide pullulan amylolysis pullulanolysis |
url |
http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390106377J.pdf |
work_keys_str_mv |
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