This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saha, B. C.
Right arrow Articles by Bothast, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saha, B. C.
Right arrow Articles by Bothast, R. J.
Agricola
Right arrow Articles by Saha, B. C.
Right arrow Articles by Bothast, R. J.

 Previous Article  |  Next Article 

Appl Environ Microbiol, January 1998, p. 216-220, Vol. 64, No. 1
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Purification and Characterization of a Novel Thermostable alpha -L-Arabinofuranosidase from a Color-Variant Strain of Aureobasidium pullulans

Badal C. Saha* and Rodney J. Bothast

Fermentation Biochemistry Research Unit, National Center for Agricultural Utilization Research, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois 61604

Received 5 August 1997/Accepted 29 October 1997

A color-variant strain of Aureobasidium pullulans (NRRL Y-12974) produced alpha -L-arabinofuranosidase (alpha -L-AFase) when grown in liquid culture on oat spelt xylan. An extracellular alpha -L-AFase was purified 215-fold to homogeneity from the culture supernatant by ammonium sulfate treatment, DEAE Bio-Gel A agarose column chromatography, gel filtration on a Bio-Gel A-0.5m column, arabinan-Sepharose 6B affinity chromatography, and SP-Sephadex C-50 column chromatography. The purified enzyme had a native molecular weight of 210,000 and was composed of two equal subunits. It had a half-life of 8 h at 75°C, displayed optimal activity at 75°C and pH 4.0 to 4.5, and had a specific activity of 21.48 µmol · min-1 · mg-1 of protein against p-nitrophenyl-alpha -L-arabinofuranoside (pNPalpha AF). The purified alpha -L-AFase readily hydrolyzed arabinan and debranched arabinan and released arabinose from arabinoxylans but was inactive against arabinogalactan. The Km values of the enzyme for the hydrolysis of pNPalpha AF, arabinan, and debranched arabinan at 75°C and pH 4.5 were 0.26 mM, 2.14 mg/ml, and 3.25 mg/ml, respectively. The alpha -L-AFase activity was not inhibited at all by L-arabinose (1.2 M). The enzyme did not require a metal ion for activity, and its activity was not affected by p-chloromercuribenzoate (0.2 mM), EDTA (10 mM), or dithiothreitol (10 mM).


* Corresponding author. Mailing address: USDA-ARS-NCAUR-FBR, 1815 N. University St., Peoria, IL 61604. Phone: (309) 681-6276. Fax: (309) 681-6686. E-mail: sahabc{at}mail.ncaur.usda.gov.




This article has been cited by other articles:

  • Klaassens, E. S., Boesten, R. J., Haarman, M., Knol, J., Schuren, F. H., Vaughan, E. E., de Vos, W. M. (2009). Mixed-Species Genomic Microarray Analysis of Fecal Samples Reveals Differential Transcriptional Responses of Bifidobacteria in Breast- and Formula-Fed Infants. Appl. Environ. Microbiol. 75: 2668-2676 [Abstract] [Full Text]  
  • Margolles, A., de los Reyes-Gavilan, C. G. (2003). Purification and Functional Characterization of a Novel {alpha}-L-Arabinofuranosidase from Bifidobacterium longum B667. Appl. Environ. Microbiol. 69: 5096-5103 [Abstract] [Full Text]  
  • Rumbold, K., Biely, P., Mastihubova, M., Gudelj, M., Gubitz, G., Robra, K.-H., Prior, B. A. (2003). Purification and Properties of a Feruloyl Esterase Involved in Lignocellulose Degradation by Aureobasidium pullulans. Appl. Environ. Microbiol. 69: 5622-5626 [Abstract] [Full Text]  
  • Lyon, P.-F., Beffa, T., Fischer, J. L., Aragno, M. (2000). Xylanase activity and thermostratification during the thermogenic phase of industrial composting in aerated trenches. Waste Manag Res 18: 174-183 [Abstract]