GASTROINTESTINAL ECOLOGY:

PROBIOTICS, PREBIOTICS AND POTENTIAL BENEFITS

 

CONTENTS

 

A.      GASTROINTESTINAL ECOLOGY

B.      PROBIOTICS

C.      PREBIOTICS

D.      NUTRITIONAL BENEFITS

F.      THERAPEUTIC ASPECTS

 

GASTROINTESTINAL TRACT

 

A.     GASTROINTESTINAL ECOLOGY

 

A1.0  Biologically important functions of Large Intestine

·       Absorption and secretion of certain electrolytes, like water.

·       Storage and excretion of waste materials.  

A2.0  Composition and activities of gut microflora           

Human Body:

·       Eukaryotic cells ≈1013

·       Prokaryotic cells ≈1014

≈50 genera with several hundred species of bacteria

         A3.0  Factors Affecting Bacterial activities  

(Cummings et al, 1991)

A4.0  GUT MICROBIAL BALANCE

    (Rotimi,1981)

          A5.0  FACTORS AFFECTING GUT MICROBIAL BALANCE

             ·       Abusive & improper dietary habits

·       Starvation

·       Alcohol consumption

·       Stress

·       Diseases of the Intestinal Tract

·       Oral antibiotic therapy

·       Surgical operation

(Wang,1993)

A6.0  COMPOSITION AND HEALTH EFFECTS OF PREDOMINANT HUMAN FECAL BACTERIA

 

 

 

 

 

 

 

 

 

 

 

 

 

A7.0  Substrates for Colonic bacterial growth  

·           Resistant Starch                   

·       Polysaccharides

·       Unabsorbed Sugars- lactose, raffinose, stachyose

·       Oligosaccharides- fructooligosaccharides, oligofructose, inulin

·       Dietary & endogenous proteins (e.g. pancreatic enzymes)

·       Sugar Alcohols – sorbitol, xylitol

·       Endogenous Carbohydrates – glycoproteins (e.g. mucin)

·       Other Food Additives

 

A8.0  Major Typ es of Metabolic Reaction

    ·           Synthesis of vitamins and amino acids.

·       Degradation of starches to simple sugars.

·       Fermentation of non-starch polysaccharides to volatile fatty acids.

·       Degradation of proteins to amino acids, amines & ammonia.

·       Hydrogenation of unsaturated fatty acids.

·       Transformation of primary to secondary bile acids.

·       Transformation of cholesterol to other sterols.

·       Reduction of nitrate to nitrite.

·       Detoxification. e.g. bilirubin to urobilins.

·       Toxin production, e.g. glycolysis of cycasin.

·       Carcinogen formation, e.g. synthesis of N- nitroso compounds.  

 

A9.    Generalized scheme of fermentation by human colonic microflora

 

 

 

 

 

 

 

 

 

 

   

 

 

 

 

(Gibsan & Raberfroid,1994)

B. PROBIOTICS

  “Organisms and substances which contribute to intestinal microbial balance”

(Sperti, 1971)

 “A live microbial feed suppliment which beneficially affects the host animal by improving its intestinal microbial balance.”

                          (Fuller, 1989)                 

 

B1.0  CRITERIA TO BE PROBIOTIC

 

1.     The probiotic must be capable of being prepared in a viable manner and on a large scale.

2.     During use and under storage the probiotic should remain viable and stable.

3.     It should be able to survive in the intestinal ecosystem.

4.     The host animal gain beneficially from harboring the probiotic.

 

B2.0  Composition of PROBIOTICS

 

Lactobacilli

Lactobacillus bulgaricus

Lactobacillus acidophilus

Lactobacillus casei

Lactobacillus helveticus

Lactobacillus lactis

Lactobacillus salivarius

Lactobacillus plantarum

Lactobacillus delbruekii

Streptococci

Streptococcus thermophilus

Streptococcus lactis

Enterococci

Enterococcus faecium

Enterococcs faecalis

Bifidobacteia

Bifidobacterium adolescentis

Bifidobacterium bifidum

Bifidobacterium infantis

Bifidobacterium longum

 

B3.    EXAMPLES OF FERMENTED MILK PRODUCTS

 

Taetmjolk

Filmjolk

Lattfil

Langfil

Maziwa lala

Ymer

Yogurt

Bulgarian Buttermilk

Yakult

 

Liquid yogurt

Aco-yogurt

Acidiphilus milk

Biogarde

Bioghurt

Bifighurt

Mil-Mile

Miru-Miru

 

 

C.     PREBIOTICS

 

A prebiotic is a non-digestible food ingredient that beneficially affects the host by selectively stimulating the growth and/or activity of one or a limited number of bacteria in the colon, and thus improves host health.

 

C1.0  Criteria for a food ingredient to be a Prebiotic

It must

·       Be neither hydrolyzed nor absorbed in the upper part of GIT.

·       Be a selective substrate for one or a limited number of beneficial bacteria in colon.

·       Be able to alter the colonic bacteria in favour of healthier composition.

·       Be able to induce beneficial systemic effects after absorption in the blood.

 

COLONIC FOOD: Compounds, not absorbed in upper GIT, or hydrolyzed by human digestive enzymes.  

C2.0  Carbohydrates as Colonic foods and Prebiotics  

Carbohydrates                                                    Colonic Foods                 Prebiotics

Resistant starch                                                              Yes                                          No

Non-starch polysaccharides

Plant cell wall polysaccharides                   Yes                                          No

Hemicelluloses                                                Yes                                          No

Pectins                                                               Yes                                          No

Gums                                                                  Yes                                          No

Non-digestable oligosaccharides

Fructooligosaccharides                                 Yes                                          Yes

Galactooligosaccharides                               Yes                                          -

Soybean oligosaccharides                              Yes                                          -

Glucooligosaccharides                                    -                                              No

 

 

 PROBIOTICS

D. NUTRITIONAL ASPECTS

 

1.0 Synthesis of B-vitamins

2.0  Improved digestibility

3.0  Anticholesterolmic effect

4.0  Improved lactose utilization

 

E. THERAPEUTICS

 

1.0  Antagonism

2.0  Antitumor activities

3.0  Constipation

4.0  Vaginitis

5.0  Diarrhea

6.0  Circulatory disorders

 

 

D1.0  SYNTHESIS OF B-VITAMINS  

B-Vitamin content of milk and cultured products (µg/100g or µg/ml)

 

MILK

YOGURT

COTTAGE CHEESE

CHEDDAR CHEESE

FOLIC ACID

Folic Acid

0.13-0.73

3.9

2.3-5.0

10.8

4-21

Biotin

2.9-4.9

4.0-5.1

3.2

2.6

0.65-2.5

Niacin

71-96

130-141

70-257

11-67

13-212

Pantothenic Acid

330-460

280-381

463

320-360

111-711

B6

17-40

---

24-56

16

49-147

B12

0.27-0.57

0.35-0.52

0.8-2.1

0.3-0.4

---


(Shahani, 1979)

D2.0  IMPROVED DIGESTIBILITY

 

D3.0  ANTICHOLESTEROLAMIC EFFECT

D3.1    SOURCE OF CHOLESTEROL  

(a)  Endogenous/ Synthesized Cholesterol

(b)  Exogenous/ Absorbed Cholesterol

  D3.2    CHOLESTEROL METABOLISM

 Synthesized Cholesterol + Dietary Cholesterol

= Faecal excretion of Cholesterol + Bile Acids

  D3.3    CHOLESTEROL REDUCTION MECHANISMS  

·       Impaired cholesterol synthesis in the body

·       Reduced absorption of dietary cholesterol

·       Stimulated catabolism of cholesterol

  D3.3.1 IMPAIRED CHOLESTEROL SYNTHESIS  

 

    D3.3.2           STIMULATED CATABOLISM OF CHOLESTEROL

  

D4.0  IMPROVED LACTOSE UTILIZATION  

LACTOSE MALABSORPTION/LACTOSE INTOLERANCE/LACTOSE MALDIGESTION:

Inability of the person to digest lactose adequately.  

 

  E1.0   ANTAGONISM

           ·       Growth inhibition of the contaminatining flora during fermentation process.

    ·       Growth inhibition of harmful intestinal micro flora after consumption of fermented products.

ANTAGONISTIC METABOLITES

ORGANIC ACIDS – Lactic acid , Acetic acid, Propionic acid

BROAD SPECTRUM ANTAGONISTS

HYDROGEN PEROXIDE (H2O2)

DIACETYL

BACTERIOCINS  

E1.1   ORGANIC ACIDS  

 

Lethality / toxicity

Organic acids > Inorganic acids

PA>AA>LA

 

E1.2   BRAOD SPECTRUM ANTAGONISTS  

General characteristics:  

·       Low molecular weight

·       Free of nitrogen

·       Acidic in nature

·       Resistant to proteolytic enzymes and heat

  LAB, associated with antagonism:  

Lactobacilli  

L. acidophilus

L. bulgaricus

L. casei

L. lactis

L. plantarum

L. brevis

L. helveticus

       

Streptococci  

S. diacetylactis

S. thermophilus  

 

Pediococci  

P. cerevisiae  

 

ACIDOPHILIN, LACTOCIDIN, ACIDOLIN

Producer: Lactobacillus acidophilus

Effective against both Gram positives and Gram negatives

 

BULGARICAN

Producer: Lactobacillus delbruckii ssp.bulgaricus

Effective against Gram positives and Gram negatives  

 

BIFIDINE

Producer: Bifidobacterium bifidum

Characteristics:

  FOOD SPOILAGE AND FOOD BORN PATHOGENS 

Escherichia coli

Pseudomonas aeruginosa

Salmonella typhimurium

Bacillus fragilis

Bacillus cereus

Proteus vulgaris

Staphylococcus aureus

Clostridium perfringens

Shigella dysentriae  

E1.3   HYDROGEN PEROXIDE

  H2O2 producer LAB Species  

SPECIES

INHIBITED CULTURES

Lactococci, Leuconostoc, Lactobacilli

Self

L. delbrueckii ssp. Lactis

Staphylococcus aureus

L. delbruekii ssp. Bulgaricus, L. plantarum

Psedomonas, Proteus, B. cereus, B. megaterium

L. acidophilus

Staphylococcus aureus, E.coli, S.typhimurium, C. perfringens

L. delbruekii ssp. Bulgaricus

Psychrotrophs

L. lactis ssp. lactis biovar. diacetylactis


Pseudomonas fragi


E1.4   DIACETYL  

Diacetyl producers  

Lactobacilli

Leuconostocs

Lactococcus lactis ssp. lactis biovar. diacetylactis

Propionibacteria

Effective Level  

Species                         effective concentration(µg/ml)

LAB                                                    >400

Gram –ves                                         ≤200

Gram +ve (non-lactic)                    >350  

Production level

       Leuconostocs                                     14 µg/ml

        Lactobacilli                                        84 µg/ml

Effectiveness of Diacetyl  

 

E1.5   BACTERIOCINS  

Anti-microbial peptides or small proteins active against bacteria closely related to the producer strain.

General Characteristics  

·       Producer strain is typically immune against its own bacteriocin.

·       Heat resistant, but are inactivated by proteolytic enzymes.

·       Bacteriocins having MW< 10 kD are small peptides, they include lantibiotic type      bacteriocins.

·       Bacteriocins have MW>30 kD are large proteins.

·       Another group of bacteriocins may be a complex molecule with a lipid or polysaccharide moiety, essentially required for its activity.

BACTERIOCIN PRODUCERS  

LACTIC ACID BACTERIA  

Lactococcus lactis

SUBSPECIES

BACTERIOCIN

INHIBITED BACTERIA

 

lactis

 

NISIN

 

Gram +ves

LACTOSTREPCINS

Other lactococci

LACTOCIN481

most lactococci, some lactobacilli,leuconostoc,clostridia

cremoris

DIPLOCOCCIN

LACTOCOCCIN A,B,M

LACTOCOCCIN A

LACTOSTREPCINS

BACTERIOCIN S50

other lactococci

 

 


Lactobacillus

SPECIES

BACTERIOCIN

INHIBITED BACTERIA

 

helveticus

 

LACTOCIN LP27

HELVETICIN J

 

-?

fermentum

FERMENTICIN

-?

acidophilus

LACTACIN F

LACTACIN B

-?

brevis

BREVICIN 37

Lactobacilli, pediococci,leuconostoc

casei

CASEICIN 80

Only L. casei B109

delbruckii, lactis

LACTICIN A, B

-?

gasseri

GASSERICIN A

-?

plantarum

PLANTACIN B

SAKACIN A

-?

sake

LACTOCIN S

-?


Leuconostoc

SPECIES

BACTERIOCIN

INHIBITED BACTERIA

 

mesenteroides

 

MESENTERICIN 5

 

Listeria monocytogens

L. ivanovii

Enterococcus faecalis

Brevibacterium lines

Pediococcus pentosaceus

But not Leuconostoc bacilli, Lactococci and Gram –ves

 

gelidum

LEUCOCIN AUAL187

most of LAB Enterococcus Faecalis, L. monocytogens

 


PROPIONIC ACID BACTERIA  

Prpionibacterium

SPECIES

BACTERIOCIN

INHIBITED BACTERIA

 

P. thoenii-P127

 

PROPIONICIN PLG-1

 

Inhibited microorganisms- PAB, pediococci, lactobacilli, lactococci, yeast and mold and gram –ve species.

 

P. jensenii P126

 

JENSENIIN G

Inhibited microorganisms PAB, Lactobacilli and Lactococci


E2.0   ANTICARCINOGENIC/ANTITUMOR ACTIVITIES  

CANCER: Set of diseases, in which uncontrolled growth of cells occur.

Types of Cancer Inhibited by Nutritional factors  

TYPE

CARCINOGEN

PREVENTION

ESOPHAGUS

tobacco, alcohol

decreased smoking & drinking

STOMACH

nitrite in food

vitamin C,E

COLON

fat, fried food, protein

increased fiber, vits, decreased fat fried foods, cultured foods

BREAST,PROSTATE

fat, fried food, hormones

decreased fat fried foods

PANCREASE

fried foods, tobacco

decreased fat fried foods, decreased smoking


   

MECHANISM OF ANTITUMOUR EFFECT

 

·        STIMULATION OF IMMUNE SYSTEM

·        INHIBITION OF TUMOUR CELLS

·        DESTRUCTION OF CARCINOGENS

·        INHIBITION OF MICROORGANISMS

 (Driessen et al, 1995)  

  STIMULATION OF IMMUNE SYSTEM

INHIBITION OF TUMOUR CELLS

DESTRUCTION OF CARCINOGENS

INHIBITION OF MICROORGANISMS


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