Terminal oxidases of Bacillus subtilis strain 168:: One quinol oxidase, cytochrome aa3 or cytochrome bd, is required for aerobic growth

被引:78
作者
Winstedt, L [1 ]
von Wachenfeldt, C [1 ]
机构
[1] Lund Univ, Dept Microbiol, SE-22362 Lund, Sweden
关键词
D O I
10.1128/JB.182.23.6557-6564.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The gram-positive endospore-forming bacterium Bacillus subtilis has, under aerobic conditions, a branched respiratory system comprising one quinol oxidase branch and one cytochrome oxidase branch. The system terminates in one of four alternative terminal oxidases. Cytochrome caa(3) is a cytochrome c oxidase, whereas cytochrome bd and cytochrome aa(3) are quinol oxidases. A fourth terminal oxidase, YthAB, is a putative quinol oxidase predicted from DNA sequence analysis. None of the terminal oxidases are, by themselves, essential for growth. However, one quinol oxidase (cytochrome aa(3) or cytochrome bd) is required for aerobic growth of B. subtilis strain 168. Data indicating that cytochrome aa(3) is the major oxidase used by exponentially growing cells in minimal and rich medium are presented. We show that one of the two heme-copper oxidases, cytochrome caa(3) or cytochrome aa(3), is required for efficient sporulation of B. subtilis strain 168 and that deletion of YthAB in a strain lacking cytochrome aa(3) makes the strain sporulation deficient.
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页码:6557 / 6564
页数:8
相关论文
共 37 条
[1]   BACTERIAL ELECTRON-TRANSPORT CHAINS [J].
ANRAKU, Y .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :101-132
[2]   A cytochrome bb′-type quinol oxidase in Bacillus subtilis strain 168 [J].
Azarkina, N ;
Siletsky, S ;
Borisov, V ;
von Wachenfeldt, C ;
Hederstedt, L ;
Konstantinov, AA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (46) :32810-32817
[3]   Molecular genetics of the genus Paracoccus:: Metabolically versatile bacteria with bioenergetic flexibility [J].
Baker, SC ;
Ferguson, SJ ;
Ludwig, B ;
Page, MD ;
Richter, OMH ;
van Spanning, RJM .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (04) :1046-+
[4]   Heme/copper terminal oxidases [J].
FergusonMiller, S ;
Babcock, GT .
CHEMICAL REVIEWS, 1996, 96 (07) :2889-2907
[5]   ANALYSIS OF SPORULATION MUTANTS .2. MUTANTS BLOCKED IN CITRIC ACID CYCLE [J].
FORTNAGEL, P ;
FREESE, E .
JOURNAL OF BACTERIOLOGY, 1968, 95 (04) :1431-+
[6]   THE SUPERFAMILY OF HEME-COPPER RESPIRATORY OXIDASES [J].
GARCIAHORSMAN, JA ;
BARQUERA, B ;
RUMBLEY, J ;
MA, JX ;
GENNIS, RB .
JOURNAL OF BACTERIOLOGY, 1994, 176 (18) :5587-5600
[7]  
Gennis R., 1996, ESCHERICHIA COLI SAL, V1, P217
[8]   THE EFFECT OF RESTRICTION ON SHOTGUN CLONING AND PLASMID STABILITY IN BACILLUS-SUBTILIS MARBURG [J].
HAIMA, P ;
BRON, S ;
VENEMA, G .
MOLECULAR & GENERAL GENETICS, 1987, 209 (02) :335-342
[9]  
HANAHAN D, 1991, METHOD ENZYMOL, V204, P63
[10]  
HEDERSTEDT L, 1986, METHOD ENZYMOL, V126, P399