Turning on and turning off the arginine deiminase system in oral streptococci

被引:33
作者
Curran, TM
Ma, YS
Rutherford, GC
Marquis, RE [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Ctr Oral Biol, Rochester, NY 14642 USA
关键词
arginine deiminase; oral streptococci; induction-derepression; acid damage; biofilms;
D O I
10.1139/cjm-44-11-1078
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 arginine deiminase system in oral streptococci is highly regulated. Il requires induction and is repressed by catabolites such as glucose or by aeration. A comparative study of regulation of the system in Streptococcus gordonii ATCC 10558, Streptococcus rattus FA-1, and Streptococcus sanguis NCTC 10904 showed an increase in activity of the system in S. sanguis of some 1467-fold associated with induction-derepression of cells previously uninduced-repressed. The activity of the system was assayed in terms of levels of arginine deiminase, the signature enzyme of the system, in permeabilized cells. Increases in enzyme levels associated with induction-derepression were Less for the other two organisms, mainly because of less severe repression. especially for S. rattus EA-I, which was the least sensitive to catabolite repression or aeration. Regulation of the arginine deiminase system involving induction and catabolite repression was demonstrated also with monoorganism biofilms composed of cells of S. sanguis adherent: to glass slides. Fully uninduced-repressed cells from suspension cultures or biofilms were compromised in their abilities to catabolize arginine to protect themselves against acid damage. However, it was found that the system can be rapidly turned on or turned off, although induction-derepression did appear to require cell growth. Still, the system could respond rapidly to the availability of arginine to reestablish high capacity for alkali production.
引用
收藏
页码:1078 / 1085
页数:8
相关论文
共 26 条
[1]  
Archibald RM, 1944, J BIOL CHEM, V156, P121
[2]  
BELLI WA, 1991, APPL ENVIRON MICROB, V57, P3540
[3]   Oral streptococci ... Products of their environment [J].
Burne, RA .
JOURNAL OF DENTAL RESEARCH, 1998, 77 (03) :445-452
[4]   CLONING AND EXPRESSION IN ESCHERICHIA-COLI OF THE GENES OF THE ARGININE DEIMINASE SYSTEM OF STREPTOCOCCUS-SANGUIS NCTC-10904 [J].
BURNE, RA ;
PARSONS, DT ;
MARQUIS, RE .
INFECTION AND IMMUNITY, 1989, 57 (11) :3540-3548
[5]  
Burne RA, 1991, GENETICS MOL BIOL ST
[6]   BAROTOLERANT VARIANT OF STREPTOCOCCUS-FAECALIS WITH REDUCED SENSITIVITY TO GLUCOSE CATABOLITE REPRESSION [J].
CAMPBELL, J ;
BENDER, GR ;
MARQUIS, RE .
CANADIAN JOURNAL OF MICROBIOLOGY, 1985, 31 (07) :644-650
[7]  
CASIANOCOLON A, 1988, APPL ENVIRON MICROB, V54, P1318
[8]   Construction and characterization of a recombinant ureolytic Streptococcus mutans and its use to demonstrate the relationship of urease activity to pH modulating capacity [J].
Clancy, A ;
Burne, RA .
FEMS MICROBIOLOGY LETTERS, 1997, 151 (02) :205-211
[9]   ARGININE DEIMINASE SYSTEM AND ACID ADAPTATION OF ORAL STREPTOCOCCI [J].
CURRAN, TM ;
LIEOU, J ;
MARQUIS, RE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (12) :4494-4496
[10]   COORDINATELY REPRESSIBLE ARGININE DEIMINASE SYSTEM IN STREPTOCOCCUS-SANGUIS [J].
FERRO, KJ ;
BENDER, GR ;
MARQUIS, RE .
CURRENT MICROBIOLOGY, 1983, 9 (03) :145-149