Bacterial, SCFA and gas profiles of a range of food ingredients following in vitro fermentation by human colonic microbiota

被引:78
作者
Beards, Emma [1 ]
Tuohy, Kieran [1 ]
Gibson, Glenn [1 ]
机构
[1] Univ Reading, Dept Food Biosci, Food Microbial Sci Unit, Reading RG6 6AP, Berks, England
关键词
Prebiotic; Microbiota; Fermentation; Enumeration; Food; CHAIN FATTY-ACIDS; SITU HYBRIDIZATION; BUTYRATE FORMATION; GUT MICROFLORA; HUMAN FECES; INULIN; METABOLISM; STARCH; OLIGOFRUCTOSE; BIFIDOBACTERIA;
D O I
10.1016/j.anaerobe.2010.05.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It is now apparent that there is a strong link between health and nutrition and this can be seen clearly when we talk of obesity. The food industry is trying to capitalise on this by adapting high sugar/fat foods to become healthier alternatives. In confectionery food ingredients can be used for a range of purposes including sucrose replacement. Many of these ingredients may also evade digestion in the upper gut and be fermented by the gut microbiota upon entering the colon. This study was designed to screen a range of ingredients and their activities on the gut microbiota. In this study we screened a range of these ingredients in triplicate batch culture fermentations with known prebiotics as controls. Changes in bacteriology were monitored using FISH. SCFA were measured by GC and gas production was assessed during anaerobic batch fermentations. Bacterial enumeration showed significant increases (P <= 0.05) in bifidobacteria and lactobacilli with polydextrose and most polyols with no significant increases in Clostridium histolyticum/perfringens. SCFA and gas formation indicated that the substrates added to the fermenters were being utilised by the gut microbiota. It therefore appears these ingredients exert some prebiotic activity in vitro. Further studies, particularly in human volunteers, are necessary. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:420 / 425
页数:6
相关论文
共 56 条
[1]   Human gut microbiota does not ferment erythritol [J].
Arrigoni, E ;
Brouns, F ;
Amadò, R .
BRITISH JOURNAL OF NUTRITION, 2005, 94 (05) :643-646
[2]   The gut microbiota as an environmental factor that regulates fat storage [J].
Bäckhed, F ;
Ding, H ;
Wang, T ;
Hooper, LV ;
Koh, GY ;
Nagy, A ;
Semenkovich, CF ;
Gordon, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (44) :15718-15723
[3]  
BEARDS EJ, 2010, BR J NUTR, V7, P1
[4]   Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut [J].
Belenguer, Alvaro ;
Duncan, Sylvia H. ;
Calder, A. Graham ;
Holtrop, Grietje ;
Louis, Petra ;
Lobley, Gerald E. ;
Flint, Harry J. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (05) :3593-3599
[5]  
BERNALIER A, 1999, COLONIC MICROBIOTA N, P27
[6]   Resistant starch lowers fecal concentrations of ammonia and phenols in humans [J].
Birkett, A ;
Muir, J ;
Phillips, J ;
Jones, G ;
ODea, K .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1996, 63 (05) :766-772
[7]   Selective increases of bifidobacteria in gut microflora improve high-fat-diet-induced diabetes in mice through a mechanism associated with endotoxaemia [J].
Cani, P. D. ;
Neyrinck, A. M. ;
Fava, F. ;
Knauf, C. ;
Burcelin, R. G. ;
Tuohy, K. M. ;
Gibson, G. R. ;
Delzenne, N. M. .
DIABETOLOGIA, 2007, 50 (11) :2374-2383
[8]   Effects of high-amylose maize starch and butyrylated high-amylose maize starch on azoxymethane-induced intestinal cancer in rats [J].
Clarke, Julie M. ;
Topping, David L. ;
Bird, Anthony R. ;
Young, Graeme P. ;
Cobiac, Lynne .
CARCINOGENESIS, 2008, 29 (11) :2190-2194
[9]  
Cook SI, 1998, ALIMENT PHARM THER, V12, P499, DOI 10.1046/j.1365-2036.1998.00337.x
[10]   Contribution of acetate to butyrate formation by human faecal bacteria [J].
Duncan, SH ;
Holtrop, G ;
Lobley, GE ;
Calder, AG ;
Stewart, CS ;
Flint, HJ .
BRITISH JOURNAL OF NUTRITION, 2004, 91 (06) :915-923