Restricted distribution of the butyrate kinase pathway among butyrate-producing bacteria from the human colon

被引:379
作者
Louis, P [1 ]
Duncan, SH [1 ]
McCrae, SI [1 ]
Millar, J [1 ]
Jackson, MS [1 ]
Flint, HJ [1 ]
机构
[1] Rowett Res Inst, Div Gut Microbiol & Immunol, Aberdeen AB21 9SB, Scotland
关键词
D O I
10.1128/JB.186.7.2099-2106.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The final steps in butyrate synthesis by anaerobic bacteria can occur via butyrate kinase and phosphotransbutyrylase or via butyryl-coenzyme A (CoA):acetate CoA-transferase. Degenerate PCR and enzymatic assays were used to assess the presence of butyrate kinase among 38 anaerobic butyrate-producing bacterial isolates from human feces that represent three different clostridial clusters (IV, XIVa, and XVI). Only four strains were found to possess detectable butyrate kinase activity. These were also the only strains to give PCR products (verifiable by sequencing) with degenerate primer pairs designed within the butyrate kinase gene or between the linked butyrate kinase/phosphotransbutyrylase genes. Further analysis of the butyrate kinase/phosphotransbutyrYlase genes of one isolate, L2-50, revealed similar organization to that described previously from different groups of clostridia, along with differences in flanking sequences and phylogenetic relationships. Butyryl-CoA:acetate CoA-transferase activity was detected in all 38 strains examined, suggesting that it, rather than butyrate kinase, provides the dominant route for butyrate formation in the human colonic ecosystem that contains a constantly high concentration of acetate.
引用
收藏
页码:2099 / 2106
页数:8
相关论文
共 54 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
ATLAS RM, 1997, HDB MICROBIOLOGICAL, P1245
[3]  
Ausubel FA, 1998, CURRENT PROTOCOLS MO
[4]   Phylogenetic relationships of butyrate-producing bacteria from the human gut [J].
Barcenilla, A ;
Pryde, SE ;
Martin, JC ;
Duncan, SH ;
Stewart, CS ;
Henderson, C ;
Flint, HJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (04) :1654-1661
[5]  
BARCENILLA A, 1999, THESIS R GORDON U AB
[6]   COENZYME-A TRANSPHORASE FROM CLOSTRIDIUM-KLUYVERI [J].
BARKER, HA ;
STADTMAN, ER ;
KORNBERG, A .
METHODS IN ENZYMOLOGY, 1955, 1 :599-602
[7]   THE CENTRAL METABOLIC PATHWAY FROM ACETYL-COA TO BUTYRYL-COA IN CLOSTRIDIUM-ACETOBUTYLICUM [J].
BENNETT, GN ;
RUDOLPH, FB .
FEMS MICROBIOLOGY REVIEWS, 1995, 17 (03) :241-249
[8]  
Benson DA, 2003, NUCLEIC ACIDS RES, V31, P23, DOI 10.1093/nar/gkg057
[9]   Molecular biological methods for studying the gut microbiota:: the EU human gut flora project [J].
Blaut, M ;
Collins, MD ;
Welling, GW ;
Doré, J ;
van Loo, J ;
de Vos, W .
BRITISH JOURNAL OF NUTRITION, 2002, 87 :S203-S211
[10]   EFFECTS OF LACTULOSE AND OTHER LAXATIVES ON ILEAL AND COLONIC PH AS MEASURED BY A RADIOTELEMETRY DEVICE [J].
BOWN, RL ;
GIBSON, JA ;
SLADEN, GE ;
HICKS, B ;
DAWSON, AM .
GUT, 1974, 15 (12) :999-1004