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Production of a novel transfructosylating enzyme from Bacillus macerans EG-6

Authors
Kim, B.W.Kwon, H.J.Park, H.Y.Nam, S.W.Park, J.P.Yun, J.W.
Issue Date
2000
Publisher
Springer Verlag
Citation
Bioprocess Engineering, v.23, no.1, pp 11 - 16
Pages
6
Journal Title
Bioprocess Engineering
Volume
23
Number
1
Start Page
11
End Page
16
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/75286
DOI
10.1007/s004499900078
ISSN
0178-515X
Abstract
A new bacterium producing a novel transfructosylating enzyme was isolated from soil and designated as Bacillus macerans EG-6. Various culture conditions for enzyme production were optimized in a flask culture. 1% (w/v) sucrose as a carbon source and a mixed nitrogen source (1% yeast extract, 1% polypeptone, and 0.5% ammonium chloride) gave the best enzyme production. Addition of phosphate and magnesium ion into the medium enhanced the enzyme yield. Optimum culture pH and temperature were 7.0 and 37°C, respectively. Under optimal culture conditions, transfructosylating enzyme was rapidly produced in the early growth period, thereafter invertase activity was predominant as the culture proceeded. Using the culture filtrate, production of fructooligosaccharides from sucrose was preliminarily carried out. In a low sucrose concentration (200 g/l), transfructosylating activity competes with invertase activity in sucrose utilization. Subsequently, low fructooligosaccharide yield (20%) was achieved due to liberation of high amounts of glucose and fructose. The best oligosaccharide yield (43%) was achieved when 500 g/l sucrose was utilized.
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