Facts 
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- Molybdenum is an essential trace element in humans and
is required for enzyme activity as a cofactor.
- Molybdenum is a transition element that can exist in multiple oxidation states and facilitate electron transfer in oxidation-reduction reactions.
- Molybdenum in foods and as soluble complexes is readily absorbed. Copper can inhibit absorption in humans.
- Under normal dietary conditions, molybdenum content of human tissue is quite low (0.1 to 1.0 mcg per gram wet weight). Liver, kidney, adrenal glands and bone contain the highest amounts of molybdenum.
- After absorption, molybdenum is rapidly excreted through the kidney (90%) and smaller amounts are excreted in bile (10%).
- In addition to the molybdenum cofactor, the other important form of molybdenum is molybdate. Evidence suggests that the molbydenum found in blood and urine exists mainly as the molybdate ion (MoO42).
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Functions 
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- Molybdenum functions mainly as an enzyme cofactor.
Three molybdoenzymes catalyze hydroxylation of various substrates.
- Aldehyde oxidase oxidizes and detoxifies various
pyrimidines, purines, pteridines, and related compounds.
- Xanthine oxidase/dehydrogenase catalyzes
transformation of hypoxanthine to xanthine, and xanthine to uric acid.
- Sulfite oxidase catalyzes the transformation of sulfite to sulfate. (Sulfite oxidase deficiency deranges cysteine metabolism).
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Deficiency signs and symptoms 
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- Molybdenum deficiency is rare, unless the diet
contains high amounts of the antagonistic substances such as, sulfate, copper
or tungstate.
- Signs of molybdenum deficiency are mouth and gum disorders, hypouricemia, hyperoxypurinemia, mental disturbance, and coma, as seen in patients with 'acquired molybdenum deficiency' resulting from parenteral methionine therapy.
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Toxicity 
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- Molybdenum is relatively non-toxic to humans.
- Symptoms such as gout (inflammation of the joints due
to accumulation of uric acid) are possible due to high blood uric acid
concentrations and accumulation of uric acid around the joints. This occurs
especially when molybdenum intakes exceed 10 to 15 mg daily.
- Gout affects primarily males over the age of 40 and occasionally, postmenopausal women. One aspect of gout related to molybdenum is decreased uric acid excretion caused by molybdenum and sulfur binding to copper in the kidneys.
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Dietary Sources 
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Milk, milk products, legumes, organ meats, and cereals are good dietary sources of molybdenum. A diet high in processed foods
may lead to a deficiency in molybdenum.
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Populations w/ Special Needs 
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There has been one recorded case of an apparent molybdenum deficiency occurring in a subject receiving total parenteral
nutrition (TPN) for 18 months due to Crohn’s disease. 3
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Requirements & Recommendations 
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Molybdenum: Dietary Reference Intake: 5
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mg/day |
Tolerable Upper Intake Levels (UL) |
Infants 0 to 6 months 7 to 12 months |
2* 3* |
ND ND |
Children 1 to 3 years 4 to 8 years |
17 22 |
300 600 |
Males 9 to 13 years 14 to 18 years 19+ years Females 9 to 13 years 14 to 18 years 19+ years |
34 43 45
34 43 45 |
1100 1700 2000
1100 1700 2000 |
Pregnancy <= 18 years 19 to 50
years |
250 50 |
1700 2000 |
Lactation <= 18 years 19 to 50
years |
50 50 |
1700 2000 |
Values are Adequate Intakes (AI). ND= Tolerable Upper Intake Levels (UL) are not determinable
due to lack of data of adverse effects in this age group and concern with regard
to lack of ability to handle excess amounts.
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Drug-Mineral Interaction 
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4 5 6- No health hazards or side effects are known.
- Caution with pregnancy or nursing, consult physician before using.
Information on the relationship between substances and disease is provided for general information, in order to convey a balanced review of the scientific literature. In many cases the relationship between a substance and a disease is tentative and additional research is needed to confirm such a relationship.
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Research Summary 
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Arthritis: Some
earlier research in the Utano National Hospital in Japan was conducted on 60
patients undergoing long-term hemodialysis. Although serum molybdenum
concentrations decreased significantly after hemodialysis, 9 patients with
dialysis related arthritis had elevated serum molybdenum concentrations.
Abnormal molybdenum accumulation may contribute to dialysis-related arthritis.
7
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