Studies on saccharification from alginate using Stenotrophomonas maltophilia

被引:9
作者
Choi, Dubok [2 ]
Ryu, Beom-Young [3 ]
Piao, Yu Lan [3 ]
Choi, Soo-Kyung [3 ]
Jo, Byung-Wook [3 ]
Shin, Woon-Seob [1 ]
Cho, Hoon [4 ]
机构
[1] Kwandong Univ, Coll Med, Dept Microbiol, Kangnung 210701, South Korea
[2] Cho Dang Univ, Dept Environm Hlth, Muan Kun 534800, Chonnam, South Korea
[3] Chosun Univ, Dept Biochem Engn, Kwangju 501759, South Korea
[4] Chosun Univ, Dept Polymer Sci & Engn, Kwangju 501759, South Korea
关键词
saccharification; alginate; Stenotrophomonas maltophilia;
D O I
10.1016/j.jiec.2007.08.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Various environmental factors affecting saccharification from alginate using Stenotrophomonas maltophilia were investigated in flask cultures. The cell concentrations increased from 0.6 to 0.92 optical density (OD) at 660 nm when the agitation rate increased from 15 to 90 rpm. On the other hand, the maximum concentration of sugar was obtained at 3.8 g/l after 4 days of culture at 15 rpm. After 3 days of preculture at 33 degrees C, the sugar concentration peaked at 5.0 g/l after 5 days of culture. When 10 g/l of NaCl was used, the maximum concentration of sugar, 5.3 g/l, was obtained after 5 days of culture. Yeast extract and peptone were the best nitrogen source for effective saccharification. Especially, the sugar concentration was 6.1 g/l after 5 days of culture using a mixture of 1.0 g/l of yeast extract and 1.0 g/l of peptone. Under optimum conditions of culture and media, scale-up for effective saccharification from alginate was carried out in 5 1 flasks. The cell concentration after 2 days of culture was 0.61 OD at 660 nm and showed no further increase after 3 days of culture. The sugar concentrations from alginate were increased with increasing culture time to 7.9 g/l after 9 days of culture. (C) 2008 Published by Elsevier B.V. on behalf of The Korean Society of Industrial and Engineering Chemistry.
引用
收藏
页码:182 / 186
页数:5
相关论文
共 15 条
  • [1] EFFECT OF DEPOLYMERIZED ALGINATES ON THE GROWTH OF BIFIDOBACTERIA
    AKIYAMA, H
    ENDO, T
    NAKAKITA, R
    MURATA, K
    YONEMOTO, Y
    OKAYAMA, K
    [J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1992, 56 (02) : 355 - 356
  • [2] BOLATITO TA, 1998, FEMS MICROBIOL LETT, V166, P165
  • [3] BOLATITO TA, 1997, BIOTECHNOL BIOENG, V53, P173
  • [4] EINAGGAR MY, 2006, J MICROBIOL, V44, P432
  • [5] Ghosh M, 2006, J MICROBIOL, V44, P473
  • [6] HAUG A, 1965, P 5 INT SEAW S STUD, P271
  • [7] BACTERIAL ALGINATE LYASE - PROPERTIES OF THE ENZYME FORMED IN A MIXED CULTURE OF BACTERIA ISOLATED FROM SOIL
    KANEKO, Y
    YONEMOTO, Y
    OKAYAMA, K
    KIMURA, A
    MURATA, K
    [J]. JOURNAL OF FERMENTATION AND BIOENGINEERING, 1990, 70 (03): : 147 - 149
  • [8] Ling LS, 2006, J MICROBIOL, V44, P439
  • [9] MULTIPLE COMPONENTS OF ENDO-POLYGULURONIDE LYASE OF PSEUDOMONAS SP
    MIN, KH
    SASAKI, SF
    KASHIWABARA, Y
    SUZUKI, H
    NISIZAWA, K
    [J]. JOURNAL OF BIOCHEMISTRY, 1977, 81 (03) : 539 - 546
  • [10] INDUCTION OF CYTOKINE PRODUCTION FROM HUMAN MONOCYTES STIMULATED WITH ALGINATE
    OTTERLEI, M
    OSTGAARD, K
    SKJAKBRAEK, G
    SMIDSROD, O
    SOONSHIONG, P
    ESPEVIK, T
    [J]. JOURNAL OF IMMUNOTHERAPY, 1991, 10 (04) : 286 - 291