Resistant starch, microbiome, and precision modulation

被引:100
作者
Dobranowski, Peter A. [1 ,2 ]
Stintzi, Alain [1 ,2 ]
机构
[1] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON, Canada
[2] Univ Ottawa, Ottawa Inst Syst Biol, Ottawa, ON, Canada
关键词
Resistant starch; microbiome; personalized therapies; personalized medicine; precision medicine; clinical trials; IN-VITRO DIGESTIBILITY; HUMAN GUT SYMBIONT; CARBOHYDRATE-BINDING MODULES; BUTYRATE-PRODUCING BACTERIA; DIETARY FIBER STRUCTURES; CHAIN FATTY-ACIDS; ALPHA-AMYLASE; BIFIDOBACTERIUM-ADOLESCENTIS; BACTEROIDES-THETAIOTAOMICRON; GRANULAR STARCH;
D O I
10.1080/19490976.2021.1926842
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Resistant starch, microbiome, and precision modulation. Mounting evidence has positioned the gut microbiome as a nexus of health. Modulating its phylogenetic composition and function has become an attractive therapeutic prospect. Resistant starches (granular amylase-resistant alpha-glycans) are available as physicochemically and morphologically distinguishable products. Attempts to leverage resistant starch as microbiome-modifying interventions in clinical studies have yielded remarkable inter-individual variation. Consequently, their utility as a potential therapy likely depends predominantly on the selected resistant starch and the subject's baseline microbiome. The purpose of this review is to detail i) the heterogeneity of resistant starches, ii) how resistant starch is sequentially degraded and fermented by specialized gut microbes, and iii) how resistant starch interventions yield variable effects on the gut microbiome.
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页数:21
相关论文
共 148 条
[1]  
Adamberg Signe, 2014, Front Nutr, V1, P21, DOI 10.3389/fnut.2014.00021
[2]   A randomized trial to determine the impact of a digestion resistant starch composition on the gut microbiome in older and mid-age adults [J].
Alfa, Michelle J. ;
Strang, David ;
Tappia, Paramjit S. ;
Graham, Morag ;
Van Domselaar, Gary ;
Forbes, Jessica D. ;
Laminman, Vanessa ;
Olson, Nancy ;
DeGagne, Pat ;
Bray, David ;
Murray, Brenda-Lee ;
Dufault, Brenden ;
Lix, Lisa M. .
CLINICAL NUTRITION, 2018, 37 (03) :797-807
[3]   BIOCHEMICAL-EVIDENCE THAT STARCH BREAKDOWN BY BACTEROIDES-THETAIOTAOMICRON INVOLVES OUTER-MEMBRANE STARCH-BINDING SITES AND PERIPLASMIC STARCH-DEGRADING ENZYMES [J].
ANDERSON, KL ;
SALYERS, AA .
JOURNAL OF BACTERIOLOGY, 1989, 171 (06) :3192-3198
[4]   Internal structure of the starch granule revealed by AFM [J].
Baker, AA ;
Miles, MJ ;
Helbert, W .
CARBOHYDRATE RESEARCH, 2001, 330 (02) :249-256
[5]   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
[6]  
Baroroh Umi, 2017, Enzyme Res, V2017, P4086845, DOI 10.1155/2017/4086845
[7]   Development of a Synbiotic Beverage Enriched with Bifidobacteria Strains and Fortified with Whey Proteins [J].
Baruzzi, Federico ;
de Candia, Silvia ;
Quintieri, Laura ;
Caputo, Leonardo ;
De Leo, Francesca .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[8]  
Baxter NT, 2019, MSPHERE, V4, DOI [10.1128/msphere.00528-18, 10.1128/mSphere.00528-18]
[9]  
Baxter NT, 2019, MBIO, V10, DOI [10.1128/mBio.02566-18, 10.1128/mbio.02566-18]
[10]   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