Isolation of Thermoanaerobacter keratinophilus sp nov., a novel thermophilic, anaerobic bacterium with keratinolytic activity

被引:101
作者
Riessen, S [1 ]
Antranikian, G [1 ]
机构
[1] Tech Univ Hamburg, Inst Tech Microbiol, D-21073 Hamburg, Germany
关键词
keratin degradation; wool; feather; Thermoanaerobacter keratinophilus; thermocetive proteases; purification;
D O I
10.1007/s007920100209
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
Several thermophilic anaerobic bacteria with keratinolytic activity growing at temperatures between 50 degreesC and 90 degreesC were isolated from samples collected on the island of Sao Miguel in the Azores (Portugal). On the basis of morphological, physiological, and 16S rDNA studies, the isolate 2KXI was identified as a new species of the genus Thermoanaerobacter, designated Thermoanaerobacter keratinophilus. This strain, which grows optimally at 70 degreesC, pH 7.0, and 0.5% NaCl, is the first member of the genus Thermoanaerabacter that has been described for its ability to degrade native keratin. Around 70% of native wool was solubilized after 10 days of incubation under anaerobic conditions. The strain was shown to possess intracellular and extracellular proteases optimally active at 60 degreesC, pH 7.0, and 85 degreesC, pH 8.0, respectively. Keratin hydrolysis was demonstrated in vitro using a sodium dodecyl sulfate gel containing feather meal. The extracellular protease responsible for breaking down keratin fibers was purified to homogeneity in only one step by applying hydxoxyapatite column chromatography. The enzyme belongs to the serine-type proteases and has a molecular mass of 135 kDa.
引用
收藏
页码:399 / 408
页数:10
相关论文
共 58 条
[51]   DETERMINATION OF DNA-BASE COMPOSITION BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
TAMAOKA, J ;
KOMAGATA, K .
FEMS MICROBIOLOGY LETTERS, 1984, 25 (01) :125-128
[52]   ISOLATION OF A KERATINOLYTIC PROTEINASE FROM TRICHOPHYTON-MENTAGROPHYTES WITH ENZYMATIC-ACTIVITY AT ACIDIC PH [J].
TSUBOI, R ;
KO, IJ ;
TAKAMORI, K ;
OGAWA, H .
INFECTION AND IMMUNITY, 1989, 57 (11) :3479-3483
[53]   Skin unhairing proteases of Bacillus subtilis: production and partial characterization [J].
Varela, H ;
Ferrari, MD ;
Belobrajdic, L ;
Vazquez, A ;
Loperena, ML .
BIOTECHNOLOGY LETTERS, 1997, 19 (08) :755-758
[54]   A first order experimental design to assess soluble proteins released by a new keratinase from Doratomyces microsporus on human substrates [J].
Vignardet, C ;
Guillaume, YC ;
Friedrich, J ;
Millet, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 191 (02) :95-102
[55]  
WEBER K, 1969, J BIOL CHEM, V244, P4406
[56]  
WIEGEL JKW, 1986, BERGEYS MANUAL SYSTE, P1379
[57]   ISOLATION, IDENTIFICATION, AND CHARACTERIZATION OF A FEATHER-DEGRADING BACTERIUM [J].
WILLIAMS, CM ;
RICHTER, CS ;
MACKENZIE, JM ;
SHIH, JCH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (06) :1509-1515
[58]   VIOLOGEN DYE INHIBITION OF METHANE FORMATION BY METHANOBACILLUS OMELIANSKII [J].
WOLIN, EA ;
WOLFE, RS ;
WOLIN, MJ .
JOURNAL OF BACTERIOLOGY, 1964, 87 (05) :993-&