Chemical modification of dextransucrase from Leuconostoc mesenteroides NRRL B-512F by pyridoxal 5′-phosphate:: Evidence for the presence of an essential lysine residue at the active site

被引:0
|
作者
Goyal, A [1 ]
Katiyar, SS [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Kanpur 208016, Uttar Pradesh, India
来源
BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL | 1998年 / 44卷 / 06期
关键词
Leuconostoc mesenteroides NRRL B-512F; dextransucrase; pyridoxal 5 '-phosphate; chemical modification;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The treatment of Leuconostoc mesenteroides NRRL B-512F dextransucrase with lysine specific reagent, pyridoxal 5'-phosphate (PLP) at pH 5.2 and 30 degrees C resulted in the loss of enzyme activity. The inactivation by PLP could be reversed completely by dilution or dialysis. Sucrose as well as acceptor substrates, glucose and dextran protected the enzyme against inactivation by PLP. A statistical, kinetic analysis of the inactivation by PLP showed that one lysine residue is essential for the enzyme activity. All these results showed that one lysine residue present at the active is essential for the activity of dextransucrase.
引用
收藏
页码:1167 / 1174
页数:8
相关论文
共 21 条
  • [1] Studies on the inactivation of Leuconostoc mesenteroides NRRL B-512F dextransucrase by o-phthalaldehyde: Evidence for the presence of an essential lysine residue at the active site
    Goyal, A
    Katiyar, SS
    JOURNAL OF ENZYME INHIBITION, 1998, 13 (02): : 147 - 160
  • [2] INACTIVATION OF LEUCONOSTOC MESENTEROIDS NRRL B-512F DEXTRANSUCRASE BY SPECIFIC MODIFICATION OF LYSINE RESIDUES WITH PYRIDOXAL-5'-PHOSPHATE
    GOYAL, A
    KATIYAR, SS
    JOURNAL OF ENZYME INHIBITION, 1995, 8 (04): : 291 - 295
  • [3] Identification of a single and non-essential cysteine residue in dextransucrase of Leuconostoc mesenteroides NRRL B-512F
    Goyal, Arun
    Tyagi, D. P.
    Katiyar, Sarvagya S.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2007, 22 (01) : 111 - 113
  • [4] Proteolytic modification of Leuconostoc mesenteroides B-512F dextransucrase
    Argüello-Morales, M
    Sánchez-González, M
    Canedo, M
    Quirasco, M
    Farrés, A
    López-Munguía, A
    ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2005, 87 (02): : 131 - 141
  • [5] Proteolytic modification of Leuconostoc mesenteroides B-512F dextransucrase
    Martha Argüello-Morales
    Mónica Sánchez-González
    Mariana Canedo
    Maricarmen Quirasco
    Amélia Farrés
    Agustín López-Munguía
    Antonie van Leeuwenhoek, 2005, 87 : 131 - 141
  • [6] Glucan binding regions of dextransucrase from Leuconostoc mesenteroides NRRL B-512F
    Funane, K
    Ookura, T
    Kobayashi, M
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1998, 62 (01) : 123 - 127
  • [7] Activity and stability of dextransucrase from Leuconostoc mesenteroides NRRL B-512F in the presence of organic solvents
    Girard, E
    Legoy, MD
    ENZYME AND MICROBIAL TECHNOLOGY, 1999, 24 (07) : 425 - 432
  • [8] Dextransucrase production by Leuconostoc mesenteroides NRRL B-1299. Comparison with L-mesenteroides NRRL B-512F
    Dols, M
    RemaudSimeon, M
    Monsan, PF
    ENZYME AND MICROBIAL TECHNOLOGY, 1997, 20 (07) : 523 - 530
  • [9] Gene encoding a dextransucrase-like protein in Leuconostoc mesenteroides NRRL B-512F
    Funane, K
    Mizuno, K
    Takahara, H
    Kobayashi, M
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2000, 64 (01) : 29 - 38
  • [10] High-level production and purification of a fully active recombinant dextransucrase from Leuconostoc mesenteroides NRRL B-512F
    Moulis, Claire
    Arcache, Audrey
    Escalier, Pierre-Claude
    Rinaudo, Marguerite
    Monsan, Pierre
    Remaud-Simeon, Magali
    Potocki-Veronese, Gabrielle
    FEMS MICROBIOLOGY LETTERS, 2006, 261 (02) : 203 - 210