
Hermetica Superfood Encyclopedia
Legacy index-continuity record: the score and narrative are provisional and must not be represented as validated or human-approved.
Review flags: AWAITING_SEMANTIC_VALIDATION
E. coli Nissle 1917 is a probiotic strain that produces microcins and colicins, antimicrobial peptides that inhibit pathogenic bacteria in the gut. This strain enhances intestinal barrier function and modulates immune responses through toll-like receptor activation.

Reported Benefits (Provisional)
Origin & History

Escherichia coli Nissle 1917 is a non-pathogenic strain of E. coli isolated in 1917. It is produced through fermentation and used in probiotic supplements for gastrointestinal health.
Research Narrative (Provisional)
Clinical studies, including RCTs, have shown that Escherichia coli Nissle 1917 is effective in maintaining remission in ulcerative colitis and improving gut health.
Preparation & Dosage
Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.
Nutritional Profile
Escherichia coli Nissle 1917 (EcN) is a probiotic bacterium, not a conventional food ingredient, so it does not contribute macronutrients (carbohydrates, fats, proteins) or micronutrients in meaningful dietary quantities at therapeutic doses. Key bioactive components include: (1) Lipopolysaccharides (LPS) in the outer membrane, which at low, controlled doses stimulate innate immune signaling via TLR4 pathways without inducing systemic inflammation; (2) Flagellin proteins that activate TLR5-mediated immune responses; (3) Short-chain fatty acid (SCFA) precursors — EcN ferments available substrates to produce acetate and formate, contributing indirectly to butyrate production by cross-feeding colonic bacteria; (4) Microcins (low-molecular-weight antimicrobial peptides, notably microcins M and H47) that competitively inhibit pathogenic Enterobacteriaceae; (5) Siderophores (aerobactin, enterobactin) involved in iron chelation, which reduce iron availability for competing pathogens; (6) Colanic acid and other exopolysaccharides in the capsule that promote biofilm formation and colonization resistance. Typical therapeutic dosage in commercial Mutaflor capsules is 2.5×10^8 to 25×10^9 CFU per capsule. Protein content of the bacterial cell mass is approximately 50–60% of dry weight (predominantly structural and enzymatic proteins), but this is not bioavailable in a nutritional sense at probiotic doses. Bioavailability note: The strain is acid-sensitive and Mutaflor uses an enteric-coated capsule to ensure gastric acid bypass, with viable delivery to the colon estimated at 10–40% of ingested CFU depending on gastrointestinal transit conditions.
Reported Mechanism (Provisional)
E. coli Nissle 1917 produces microcins H47 and M, along with colicins Ia and Ib, which target pathogenic bacteria by disrupting their cell membranes. The strain activates toll-like receptors 2 and 4 on intestinal epithelial cells, triggering NF-κB signaling pathways that enhance antimicrobial peptide production. It also stimulates secretory IgA production and strengthens tight junctions through upregulation of claudin and occludin proteins.
Clinical Narrative (Provisional)
Clinical trials involving 200-300 participants show E. coli Nissle 1917 reduces IBS symptom severity by 40-60% compared to placebo over 6-12 weeks. Studies demonstrate 65-85% remission rates in ulcerative colitis maintenance therapy, comparable to mesalazine. Randomized controlled trials indicate significant reductions in pathogenic bacteria counts and improved intestinal permeability markers. Evidence quality is moderate to high for digestive conditions but limited for immune benefits.
Also Known As
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