Viability staining and terminal deoxyribonucleotide transferase-mediated dUTP nick end labelling of the mycelium in submerged cultures of Streptomyces antibioticus ETH7451

被引:15
作者
Fernandez, M [1 ]
Sanchez, J [1 ]
机构
[1] Fac Med, Area Microbiol, Oviedo 33006, Spain
关键词
Streptomyces; submerged culture; death process; viability staining; TUNEL;
D O I
10.1016/S0167-7012(01)00332-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Viability stain and terminal deoxyribonucleotide transferase-mediated dUTP nick end labelling (TUNEL) have been applied to submerged cultures of Streptomyces antibioticus ETH7451, the last technique after a suitable permeabilization treatment. Areas of dead mycelium can be clearly delineated by the viability stain within the network of hyphae which forms the mycelial masses characteristic of the submerged cultures. In addition. the TUNEL reaction shows that DNA fragmentation accompanies the death processes in the mycelium. These techniques permit the investigation of the influence of the medium and nutritional conditions on the viability of the cells. This has relevant biotechnological implications for the study of these important filamentous bacteria in the industrial fermentation processes. These techniques also allow a straighforward analysis of the physical and chemical reagents which provoke damage in Streptomyces DNA. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:293 / 298
页数:6
相关论文
共 16 条
[1]   MYCELIAL MORPHOLOGY AND METABOLITE PRODUCTION [J].
BRAUN, S ;
VECHTLIFSHITZ, SE .
TRENDS IN BIOTECHNOLOGY, 1991, 9 (02) :63-68
[2]  
DARZYNKIEWICZ Z, 1994, METHOD CELL BIOL, V41, P15
[3]  
FERNANDEZ M, 2001, UNPUB EFFECTS 5 AZAC, pB96
[4]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[5]  
GUMPERT J, 1985, BIOL BIOCH BIOMEDICA, P453
[6]  
GUMPERT J, 1978, NOCARDIA STREPTOMYCE, P221
[7]   DETECTION OF MESSENGER-RNA IN STREPTOMYCES CELLS BY WHOLE-CELL HYBRIDIZATION WITH DIGOXIGENIN-LABELED PROBES [J].
HAHN, D ;
AMANN, RI ;
ZEYER, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (08) :2753-2757
[8]  
Haugland RP., 1999, HDB FLUORESCENT PROB
[9]  
ILLING GT, 1989, J GEN MICROBIOL, V135, P2289
[10]   Heterogeneous distribution of lysine 6-aminotransferase during cephamycin C biosynthesis in Streptomyces clavuligerus demonstrated using green fluorescent protein as a reporter [J].
Khetan, A ;
Hu, WS ;
Sherman, DH .
MICROBIOLOGY-UK, 2000, 146 :1869-1880