Macfarlane Sandra, Macfarlane George T
University of Dundee, MRC Microbiology and Gut Biology Group, Ninewells Hospital Medical School, Dundee DD1 9SY, UK.
Proc Nutr Soc. 2003 Feb;62(1):67-72. doi: 10.1079/PNS2002207.
Short-chain fatty acid (SCFA) formation by intestinal bacteria is regulated by many different host, environmental, dietary and microbiological factors. In broad terms, however, substrate availability, bacterial species composition of the microbiota and intestinal transit time largely determine the amounts and types of SCFA that are produced in healthy individuals. The majority of SCFA in the gut are derived from bacterial breakdown of complex carbohydrates, especially in the proximal bowel, but digestion of proteins and peptides makes an increasing contribution to SCFA production as food residues pass through the bowel. Bacterial hydrogen metabolism also affects the way in which SCFA are made. This outcome can be seen through the effects of inorganic electron acceptors (nitrate, sulfate) on fermentation processes, where they facilitate the formation of more oxidised SCFA such as acetate, at the expense of more reduced fatty acids, such as butyrate. Chemostat studies using pure cultures of saccharolytic gut micro-organisms demonstrate that C availability and growth rate strongly affect the outcome of fermentation. For example, acetate and formate are the major bifidobacterial fermentation products formed during growth under C limitation, whereas acetate and lactate are produced when carbohydrate is in excess. Lactate is also used as an electron sink in Clostridium perfringens and, to a lesser extent, in Bacteroides fragilis. In the latter organism acetate and succinate are the major fermentation products when substrate is abundant, whereas succinate is decarboxylated to produce propionate when C and energy sources are limiting.
肠道细菌产生短链脂肪酸(SCFA)的过程受多种不同的宿主、环境、饮食和微生物因素调控。然而,总体而言,底物可用性、微生物群的细菌种类组成以及肠道转运时间在很大程度上决定了健康个体中产生的SCFA的数量和类型。肠道中的大多数SCFA源自复杂碳水化合物的细菌分解,尤其是在近端肠道,但随着食物残渣在肠道中移动,蛋白质和肽的消化对SCFA产生的贡献越来越大。细菌氢代谢也会影响SCFA的生成方式。这一结果可通过无机电子受体(硝酸盐、硫酸盐)对发酵过程的影响看出,在发酵过程中,它们会促进更多氧化型SCFA(如乙酸盐)的形成,代价是减少更多还原型脂肪酸(如丁酸盐)的生成。使用解糖型肠道微生物纯培养物进行的恒化器研究表明,碳可用性和生长速率会强烈影响发酵结果。例如,在碳限制条件下生长时,乙酸盐和甲酸盐是双歧杆菌的主要发酵产物,而当碳水化合物过量时则会产生乙酸盐和乳酸盐。乳酸盐在产气荚膜梭菌中也用作电子受体,在脆弱拟杆菌中作用较小。在后者中,当底物丰富时,乙酸盐和琥珀酸盐是主要发酵产物,而当碳和能源有限时,琥珀酸盐会脱羧生成丙酸盐。