Characterization of Novel Amylase from Amylolytic Lactic Acid Bacteria Pediococcus ethanolidurans Isolated from Japanese Pickles (Nuka-zuke)

被引:9
作者
Iuchi, Ayaka [1 ]
Haruguchi, Sachi [1 ]
Mongkolthanaruk, Wiyada [2 ]
Arima, Jiro [1 ]
Nagase, Mitsutoshi [3 ]
Hoang Quoc Khanh [4 ]
Ichiyanagi, Tsuyoshi [1 ]
Yamaguchi, Takeshi [1 ]
Shimomura, Norihiro [1 ]
Aimi, Tadanori [1 ]
机构
[1] Tottori Univ, Fac Agr, Tottori 6808553, Japan
[2] Khon Kaen Univ, Fac Sci, Khon Kaen 40002, Thailand
[3] Shimane Inst Ind Technol, Matsue, Shimane 6900816, Japan
[4] Viet Nam Acad Sci & Technol, Inst Trop Biol, Ho Chi Minh City, Vietnam
关键词
amylase; nuka-zuke; Pediococcus ethanolidurans; lactic acid bacteria; NaCl; MEDIUM PUMP SYSTEM; ALPHA-AMYLASE; PURIFICATION;
D O I
10.3136/fstr.18.861
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, Pediococcus ethanolidurans A4-27 was isolated from Japanese pickles (nuka-zuke). The bacteria produce high molecular weight amylase. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and zymogram activity staining showed a single band at around 150 kDa. The enzyme was purified by disc preparative native-polyacrylamide gel electrophoresis, and ion chromatograph analysis of reaction products of P ethanolidurans amylase on starch showed that glucose and maltose are the main final products. The appearance of maltose and glucose as major hydrolysis products suggests that the amylase produced by this organism is of a-type. Optimal temperature and pH for the enzyme activity were 60 C and pH 4.0 6.0, respectively. Enzyme activity was not affected by the presence of 10 mM calcium chloride (Ca2+) or the presence of 1000 mM and 2000 mM NaCl. These results indicate that the amylase from ethanolidurans is a useful enzyme for fermentation of rice bran-bed (nuka-doko) containing more than 15% NaCl.
引用
收藏
页码:861 / 867
页数:7
相关论文
共 22 条
  • [1] Purification and characterization of an extracellular α-amylase produced by Lactobacillus manihotivorans LMG 18010T, an amylolytic lactic acid bacterium
    Aguilar, G
    Morlon-Guyot, J
    Trejo-Aguilar, B
    Guyot, JP
    [J]. ENZYME AND MICROBIAL TECHNOLOGY, 2000, 27 (06) : 406 - 413
  • [2] [Anonymous], 2005, PHYLIP (phylogeny inference package) version 3.6
  • [3] A novel thermostable, acidophilic α-amylase from a new thermophilic "Bacillus sp Ferdowsicous" isolated from Ferdows hot mineral spring in Iran: Purification and biochemical characterization
    Asoodeh, Ahmad
    Chamani, JamshidKhan
    Lagzian, Milad
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2010, 46 (03) : 289 - 297
  • [4] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [5] Cho, 2007, J MICROBIOL BIOTECHN, V17, P1521
  • [6] PURIFICATION AND CHARACTERIZATION OF AN EXTRACELLULAR AMYLASE FROM LACTOBACILLUS-PLANTARUM STRAIN A6
    GIRAUD, E
    GOSSELIN, L
    MARIN, B
    PARADA, JL
    RAIMBAULT, M
    [J]. JOURNAL OF APPLIED BACTERIOLOGY, 1993, 75 (03): : 276 - 282
  • [7] Further development of an electroosmotic medium pump system for preparative disk gel electrophoresis
    Hayakawa, M
    Hosogi, Y
    Takiguchi, H
    Shiroza, T
    Shibata, Y
    Hiratsuka, K
    Kiyama-Kishikawa, M
    Hamajima, S
    Abiko, Y
    [J]. ANALYTICAL BIOCHEMISTRY, 2003, 313 (01) : 60 - 67
  • [8] Evaluation of the electroosmotic medium pump system for preparative disk gel electrophoresis
    Hayakawa, M
    Hosogi, Y
    Takiguchi, H
    Saito, S
    Shiroza, T
    Shibata, Y
    Hiratsuka, K
    Kiyama-Kishikawa, M
    Abiko, Y
    [J]. ANALYTICAL BIOCHEMISTRY, 2001, 288 (02) : 168 - 175
  • [9] A Novel α-Amylase from Bacillus mojavensis A21: Purification and Biochemical Characterization
    Hmidet, Noomen
    Maalej, Hana
    Haddar, Anissa
    Nasri, Moncef
    [J]. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2010, 162 (04) : 1018 - 1030
  • [10] PRODUCTION AND SEPARATION OF PEPTIDES FROM PROTEINS STAINED WITH COOMASSIE BRILLIANT BLUE R-250 AFTER SEPARATION BY SODIUM DODECYL-SULFATE POLYACRYLAMIDE-GEL ELECTROPHORESIS
    KAWASAKI, H
    EMORI, Y
    SUZUKI, K
    [J]. ANALYTICAL BIOCHEMISTRY, 1990, 191 (02) : 332 - 336