Xylose isomerase

Nutrient group: Enzymes

Sources and physiological effects

Dietary sources
The enzyme xylose isomerase  catalyzes the rearrangement of aldoses to ketoses and vice versa. It is primarily obtained from microorganisms and is mainly used for the production of glucose-fructose syrups from corn starch. The enzyme is not found in foods.
Physiological effects
 Intestinal sugar utilization
  • Catalyzes the reversible shift from fructose to glucose

 

Detailed information

Fructose malabsorption
Fructose is found in many fruits and vegetables, fruit juices and honey. It is also a component of household sugar (sucrose) and is added to various foods as a sweetener. Intestinal fructose malabsorption is based on a disturbed function of the transport protein GLUT 5 in the mucous membrane of the small intestine, so that fructose supplied with food is not sufficiently absorbed (1). It reaches the lower intestinal sections, where the enzymatic degradation of fructose by intestinal bacteria leads to gas formation and diarrhea. The frequency of intestinal fructose malabsorption is reported to be 36% for Europeans, 50% of whom show clinical symptoms.
Enzymatic support of fructose degradation
The enzyme xylose isomerase (XI) can convert fructose from food into easily digestible glucose. The dietary intake of XI promotes fructose degradation and reduces the amount of fructose in the small intestine.
Depression due to fructose malabsorption
Fructose forms complexes with tryptophan in the intestine, resulting in a lack of uptake of this essential amino acid (2). Tryptophan is a key substance for the biosynthesis of the neurotransmitter serotonin, which among other things has an important influence on the mood (“happiness hormone“). This explains why patients with fructose malabsorption have a significantly higher tendency toward depression (3)(4). Increased irritability, restlessness and headaches can also be observed in connection with fructose malabsorption. In addition to the impairment of mood, lowered folic acid and serum zinc levels are also observed.

 

Reference values

Substrate Parameter Reference value Description
 Stool Fructose cleavage activity in stool > 8.9 g/l  Analysis of bacterial cleavage activity in a stool sample (also possible for sorbitol/xylitol)
Breath H2-Breath test  Difference to initial value < 15 ppm H Hydrogen produced in the intestine during the decomposition of fructose is measured in the exhaled air.

 

Deficiency symptoms

Effect on Symptoms
General condition Headache, agitation, irritability, depression
Gastrointestinal system flatulence, pain, diarrhea (also alternating with constipation)

Indications

Effect Indication Dosing
Physiological effects
at a low intake
For targeted degradation of fructose into easily usable glucose in fructose malabsorption 30 - 100 mg/d 

 

Administration

General mode of administration
 
When
 
Xylo-isomerase should be taken immediately before a high fructose meal.
Side effects
There are no known side effects to date.
Contraindications
There are no known contraindications to date.

Interactions

Drug or nutrient interactions

 None

No relevant interactions are known to date.

 

References

References

(1) Ledochowski M et al. Kohlenhydratmalabsorptionssyndrome. Ernährungsmedizin. Hrsg. Widhalm K, Diallo-Ginstl E, Wien: ÖÄK-Verlag 2000.
(2) Ledochowski M et al. Fructose malabsorption is associated with decreased plasma tryptophan. Scan J Gastroenterol 2001; 36(4): 367-371.
(3) Ledochowski M et al. Carbohydrat malabsorption syndroms and early signs of mental depression in females. Digest Dis Sci 2000; 45(7): 1255-1259.
(4) Varea V et al. Malabsorption of carbohydrates and depression in children and adolescents. J Ped Gastroent Nutr 2005; 40(5): 561-565.


 References Interactions:
(1) Stargrove Mitchell Bebel, Treasure Jonathan, McKee Dwight L.: Herb, Nutrient, and Drug Interactions: Clinical Implications and Therapeutic Strategies. 2008
(2) Gröber Uwe: Mikronährstoffe. Metabolic Tuning – Prävention – Therapie. 3. Auflage, 2011
(3) Gröber Uwe: Arzneimittel und Mikronährstoffe. Medikationsorientierte Supplementierung. 2. Auflage, 2012

 

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