Kluyveromyces phaffii killer toxin active against wine spoilage yeasts:: purification and characterization

被引:55
作者
Comitini, F [1 ]
Di Pietro, N [1 ]
Zacchi, L [1 ]
Mannazzu, I [1 ]
Ciani, M [1 ]
机构
[1] Univ Politecn Marche, Dipartimento Sci Alimenti, I-60131 Ancona, Italy
来源
MICROBIOLOGY-SGM | 2004年 / 150卷
关键词
D O I
10.1099/mic.0.27145-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The killer toxin secreted by Kluyveromyces phaffii (KpKt) is active against spoilage yeast under winemaking conditions and thus has potential applications in the biocontrol of undesired micro-organisms in the wine industry. Biochemical characterization and N-terminal sequencing of the purified toxin show that KpKt is a glycosylated protein with a molecular mass of 33 kDa. Moreover, it shows 93% and 80% identity to a beta-1,3-glucanase of Saccharomyces cerevisiae and a beta-1,3-glucan transferase of Candida albicans, respectively, and it is active on laminarin and glucan, thus showing a beta-glucanase activity. Competitive inhibition of killer activity by cell-wall polysaccharides suggests that glucan (beta-1,3 and beta-1,6 branched glucans) represents the first receptor site of the toxin on the envelope of the sensitive target. Flow cytometry analysis of the sensitive target after treatment with KpKt and K1 toxin of S. cerevisiae, known to cause loss of cell viability via formation of pores in the cell membrane, suggests a different mode of action for KpKt.
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收藏
页码:2535 / 2541
页数:7
相关论文
共 50 条
[1]   A molecular target for viral killer toxin: TOK1 potassium channels [J].
Ahmed, A ;
Sesti, F ;
Ilan, N ;
Shih, TM ;
Sturley, SL ;
Goldstein, SAN .
CELL, 1999, 99 (03) :283-291
[2]  
[Anonymous], 1993, WINE MICROBIOLOGY BI
[3]  
Boekhout T, 1997, J MED VET MYCOL, V35, P147
[4]  
BOONE C, 1990, AM J ENOL VITICULT, V41, P37
[5]   YEAST KILLER FACTOR - ATP LEAKAGE AND COORDINATE INHIBITION OF MACROMOLECULAR SYNTHESIS IN SENSITIVE CELLS [J].
BUSSEY, H ;
SHERMAN, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 298 (04) :868-875
[6]   Large-scale screening of selected Candida maltosa, Debaryomyces hansenii and Pichia anomala killer toxin activity against pathogenic yeasts [J].
Buzzini, P ;
Martini, A .
MEDICAL MYCOLOGY, 2001, 39 (06) :479-482
[7]   Inhibition by yeast killer toxin-like antibodies of oral streptococci adhesion to tooth surfaces in an ex vivo model [J].
Conti, S ;
Magliani, W ;
Arseni, S ;
Frazzi, R ;
Salati, A ;
Ravanetti, L ;
Polonelli, L .
MOLECULAR MEDICINE, 2002, 8 (06) :311-315
[8]   Overexpression of Pex15p, a phosphorylated peroxisomal integral membrane protein required for peroxisome assembly in S-cerevisiae, causes proliferation of the endoplasmic reticulum membrane [J].
Elgersma, Y ;
Kwast, L ;
van den Berg, M ;
Snyder, WB ;
Distel, B ;
Subramani, S ;
Tabak, HF .
EMBO JOURNAL, 1997, 16 (24) :7326-7341
[9]   KINETICS OF BETA-1,3 GLUCAN INTERACTION AT THE DONOR AND ACCEPTOR SITES OF THE FUNGAL GLUCOSYLTRANSFERASE ENCODED BY THE BGL2 GENE [J].
GOLDMAN, RC ;
SULLIVAN, PA ;
ZAKULA, D ;
CAPOBIANCO, JO .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 227 (1-2) :372-378
[10]   RAPID-DETERMINATION OF ANTIFUNGAL ACTIVITY BY FLOW-CYTOMETRY [J].
GREEN, L ;
PETERSEN, B ;
STEIMEL, L ;
HAEBER, P ;
CURRENT, W .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (04) :1088-1091