Enzymic Activity in Ileostomy Effluent with reference to the Characteristic Flora

References

• Allen A. Structure of gastrointestinal mucus glycoproteins and the viscous and gel-forming properties of mucus. British Medical Bulletin 1978; 34: 28–33
   PubMedGoogle Scholar
• Allen A. Structure & Function of gastrointestinal mucins. Physiology of the Intestinal Tract., R F. Johnson. Raven, New York 1981; 617–639
   Google Scholar
• Bayliss C E., Houston P A. Characterization of plant polysaccharide-and mucin-fermenting anaerobic bacteria from human faeces. Applied and Environmental Microbiology 1984; 48: 626–632
   PubMed Web of Science ®Google Scholar
• Berghouse L, Hori S, Hill M, Hudson M, Lennard-Jones J E., Rogers E. Comparison between the bacterial and oligosaccharide content of ileostomy effluent in subjects taking diets rich in refined or unrefined carbohydrate. Gut 1984; 25: 1071–1077
   PubMed Web of Science ®Google Scholar
• Corrodi P, Wideman P A., Sutter V L., Drenick E J., Passaro E, Jr, Finegold S M. Bacterial flora of the small bowel before and after bypass procedure for morbid obesity. Journal of Infectious Diseases 1978; 137: 1–6
   PubMed Web of Science ®Google Scholar
• Cummings J H. Fermentation in the human large intestine: evidence and implications for health. Lancet 1983; i: 1206–1209
   Google Scholar
• Fernandez F, Kennedy H, Hill M, Truelove S. The effect of diet on the composition of the bacterial flora on the terminal ileum. Models of Anaerobic Infection., M J. Hill. Martinus Nijhoff, Boston 1984; 252–253
   Google Scholar
• Finegold S M., Sutter V L., Boyle J D., Shimada K. The normal flora of ileostomy and transverse colostomy effluents. Journal of Infectious Diseases 1970; 122: 376–381
   PubMed Web of Science ®Google Scholar
• Genell S, Gustafsson B A., Ohlsson K. Quantitation of active pancreatic endopeptidases in the intestinal contents of germfree and conventional rats. Scandinavian Journal of Gastroenterology 1976; 11: 757–762
   PubMed Web of Science ®Google Scholar
• Gibson S AW, MacFarlane G T. Studies on the proteolytic activity of Bacteroides fragilis. Journal of General Microbiology 1988; 134: 19–27
   PubMedGoogle Scholar
• Gibson A WS, McFarlan C, Hay S, McFarlane G T. Significance of microflora in proteolysis in the colon. Applied and Environmental Microbiology 1989; 55: 679–683
   PubMed Web of Science ®Google Scholar
• Gorbach S L., Nahas L, Weinstein L. Studies on intestinal microflora. IV. The microflora of ileostomy effluent: a unique microbial ecology. Gastroenterology 1967; 53: 874–881
   PubMed Web of Science ®Google Scholar
• Holdeman L V., Good I J., Moore W EC. Human faecal flora: variation in bacterial composition within individuals and a possible effect of emotional stress. Applied Environmental Microbiology 1976; 31: 359–375
   PubMed Web of Science ®Google Scholar
• Holdeman L V., Cato E P., Moore W EC. Anaerobe Laboratory Manual, 4th edn. V.P.I. Anaerobe Laboratory, Virginia Polytechnic Institute and State University, Blacksbury, VA 1977
   Google Scholar
• Hoskins L C., Boulding E T. Degradation of blood group antigens in human colon ecosystems. II A gene interaction in man that affects the faecal population density of certain enteric bacteria. Journal of Clinical Investigation 1976; 57: 74–82
   Web of Science ®Google Scholar
• Hoskins L C., Boulding E T. Mucin degradation in human colon systems. Evidence for the existence and role of bacterial subpopulations producing glycosidases as extracellular enzymes. Journal of Clinical Investigation 1981; 67: 163–172
   PubMed Web of Science ®Google Scholar
• Kelly D G., Phillips S F., Kelly K A., Weinstein W M., Gilchrist M JR. Dysfunction of the continent ileostomy: clinical features and bacteriology. Gut 1983; 24: 193–201
   PubMed Web of Science ®Google Scholar
• MacFarlane G T., Allison C, Gibson S AW, Cummings J H. Contribution of the micro-flora to proteolysis in the human large intestine. Journal of Applied Bacteriology 1988; 64: 37–46
   PubMedGoogle Scholar
• Moore W EC, Holdeman L V. Human faecal flora: the normal flora of 20 Japanese-Hawaiians. Applied Microbiology 1974; 27: 961–979
   PubMedGoogle Scholar
• Neale G, Hopkins J R., Peach S, Tabaqchali S. Measurement of glycosidase activities in faeces (abstract). Gut 1978; 19: A457
   Web of Science ®Google Scholar
• Norin K E., Gustafsson B E., Lindblad B S., Midtvedt T. The establishment of some microflora associated biochemical characteristics in faeces from children during the first year of life. Acta Paediatrica Scandinavica 1985; 74: 207–212
   PubMed Web of Science ®Google Scholar
• Olaison G, Sjödahl R, Leandersson P, Tagesson C. Abnormal intestinal permeability patterns in colonic Crohn's disease. Scandinavian Journal of Gastroenterology 1989; 24: 571–576
   PubMed Web of Science ®Google Scholar
• Rowland I R., Mallet A K., Wise A. The effluent of diet on the mammalian gut flora and its metabolic activities. CRC Critical Reviews in Toxicology 1985; 16: 31–103
   Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Both-Patoir H C. Anaerobic gram-negative faecal flora in patients with Crohn's disease & healthy subjects. Antonie Leeuwenhoek 1983; 49: 125–132
   PubMed Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Both-Patoir H C. The applicability of redox-indicator dyes in strongly reduced media: their effect on the human faecal flora. FEMS Microbiology Letters 1985; 28: 341–345
   Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Van Lieshout L MC. Increased faecal glycosidases in patients with Crohn's disease. Digestion 1987; 37: 43–50
   PubMed Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Van Lieshout L MC. Increased proteolysis and leucine aminopeptidase activity in faeces of patients with Crohn's disease. Digestion 1988; 40: 33–40
   Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Van der Helm R, Van Lieshout L MC. Degradation of intestinal glycoproteins by Bacteroides vulgatus. FEMS Microbiology Letters 1989; 58: 37–42
   Web of Science ®Google Scholar
• Ruseler-van Embden J GH, Van der Helm R, Van Lieshout L MC. Glycolytic and proteolytic activity in gnotobiotic rats, monoassociated with Bacteroides vulgatus. Microecology and Therapy 1988; 18: 253–259
   Google Scholar
• Siegel S. Nonparametric Statistics for the Behavioral Sciences. McGraw-Hill, London 1956
   Google Scholar
• Thadepalli H, Sister M AL, Bach V T., Matsui T K., Mandal A K. Microflora of the human small intestine. American Journal of Surgery 1979; 138: 845–850
   PubMed Web of Science ®Google Scholar
• Variyam E P., Hoskins L C. Degradation of gut mucins; carbohydrate side chains protect the polypeptide core from pancreatic elastase (abstract). Gastroenterology 1978; 74: 1108
   Web of Science ®Google Scholar
• Warren L. The thiobarbituric acid assay of sialic acids. Journal of Biological Chemistry 1959; 234: 1971–1975
   PubMed Web of Science ®Google Scholar
• Wensinck F, Ruseler-van Embden J GH. The intestinal flora of colonization-resistant mice. Journal of Hygiene, Cambridge 1971; 69: 413–421
   PubMedGoogle Scholar
• Wensinck F, Custers-van Lieshout L MC, Poppelaars-Kustermans P AJ, Schröder A M. The faecal flora of patients with Crohn's disease. Journal of Hygiene, Cambridge 1981; 87: 1–12
   PubMedGoogle Scholar
• Wesley A W., Forstner J F., Forstner G G. Structure of intestinal-mucus glycoproteins from human post-mortem or surgical tissue: inferences from correlation analysis of sugar and sulfate composition of individual mucins. Carbohydrate Research 1983; 115: 151–163
   Web of Science ®Google Scholar