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Production of 3,6-anhydro-L-galactose from agarose by agarolytic enzymes of Saccharophagus degradans 2-40

Authors
Yun, Eun JuShin, Min HyeYoon, Jeong-JunKim, Yong JinChoi, In-GeolKim, Kyoung Heon
Issue Date
1월-2011
Publisher
ELSEVIER SCI LTD
Keywords
3,6-Anhydro-L-galactose; Saccharophagus degradans; Agarase; Red macroalgae; Gas chromatography-mass spectrometry
Citation
PROCESS BIOCHEMISTRY, v.46, no.1, pp.88 - 93
Indexed
SCIE
SCOPUS
Journal Title
PROCESS BIOCHEMISTRY
Volume
46
Number
1
Start Page
88
End Page
93
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/113442
DOI
10.1016/j.procbio.2010.07.019
ISSN
1359-5113
Abstract
Saccharophagus degradans 2-40 is capable of hydrolyzing agarose, a red macroalgae-derived polymer, into D-galactose and 3,6-anhydro-L-galactose (L-AHG). Its agarase system is receiving much attention because it can be used to produce fermentable sugar from agarose. L-AHG is commercially unavailable and is considered a rare sugar with a high value. In this study, cells grown on agarose, agar or red macroalgae biomass were found to have a significantly higher agarase activity and AHG-generating activity than those grown on glucose or galactose. From agar-grown cells, both the volumetric activities of agarases and AHG generation in the cell-free lysate were much higher than in the extracellular fraction. Based on the analyses of the enzyme reaction products, from the reaction with the crude enzymes from cell-free lysate, neoagarobiose with a degree of polymerization (DP) 2 appeared to be the only major product in the initial reaction period, but sugars with DPs 2, 4 and 6 were found to be all predominantly produced by the extracellular enzymes in the initial reaction period. Quantitative analysis of AHG using gas chromatography-mass spectrometry with a derivatization step was also found to be highly reproducible and reliable. These results will be useful for producing L-AHG as a rare sugar to investigate its metabolic fate and commercial utilization. (C) 2010 Elsevier Ltd. All rights reserved.
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