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Differential degradation of apple cell walls in vitro by enzyme extracts from Botrytis cinerea and Glomerella cingulata
Year:
1997
Source of publication :
Carbohydrate Polymers
Authors :
Ben-Shalom, Noach
;
.
Pinto, Rivka
;
.
Volume :
33
Co-Authors:
Ben-Shalom, N., Department of Food Science, Volcani Center, ARO, Bet Dagan, Israel
Conway, W.S., Hort. Crops Quality Laboratory, Prod. Qual. and Devmt. Institute, USDA, Beltsville, MD 20705-2350, United States
Gross, K.C., Hort. Crops Quality Laboratory, Prod. Qual. and Devmt. Institute, USDA, Beltsville, MD 20705-2350, United States
Sams, C.E., Department of Plant and Soil Science, University of Tennessee, Knoxville, TN 37901, United States
Pinto, R., Department of Food Science, Volcani Center, ARO, Bet Dagan, Israel
Facilitators :
From page:
109
To page:
113
(
Total pages:
5
)
Abstract:
Growth and associated glycosidase enzyme production and activity of Botrytis cinerea and Glomerella cingulata were compared in vitro using apple cell walls as a carbon source. In liquid culture, the growth of the two pathogens was similar. Both fungi produced α-L-arabinosidase but β-D-galactosidase activity was higher in B. cinerea. In vitro degradation of apple cell walls by enzyme extracts from liquid cultures of G. cingulata was greater than for B. cinerea. After 24h of incubation, the G. cingulata extract solubilized 69% of the total cell wall neutral sugar and 78% of the total uronic acid, while the B. cinerea extract solubilized only 43% of the neutral sugar and 37% of the uronic-acid-containing wall polymers. The neutral sugar composition of the residue remaining after degradation (the products left after the activity of the respective fungal enzymes) differed between the two fungi. © 1997 Elsevier Science Ltd.
Note:
Related Files :
Botryotinia fuckeliana
Botrytis
Cingulata
fungi
Glomerella cingulata
Malus x domestica
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DOI :
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
25187
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:13
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