Skip to content
AlternativeMed

Histidine, Methionine, Phenylalanine, Threonine and Valine: Roles, Food Sources and Supplements

Roles, food sources and supplement questions for five essential amino acids: histidine, methionine, phenylalanine, threonine and valine, including PKU and aspartame, homocysteine and what is not known.

Content last updated . This page has not been medically reviewed.

Food sources and official figures

Amino acids come from animal foods such as meat, milk, fish and eggs and from plant foods such as soy, beans, legumes, nut butters and some grains. [4] Methionine and threonine generally occur in low amounts in plant products and are enriched in animal products. [5] Phenylalanine is found in all proteins. [2]

Verified daily requirements for these five amino acids from NIH ODS, EFSA, the NHS, MedlinePlus or Health Canada were not found, so none is quoted. Health Canada does give a scoring pattern for judging food protein (people aged 1 year and over, mg of amino acid per gram of protein): histidine 18, methionine plus cysteine 25, phenylalanine plus tyrosine 47, threonine 27, valine 32. [6] It is a yardstick for food protein, not a target for any person. A 2025 systematic review found limited requirement studies across life stages, especially pregnancy, infancy and childhood. [7]

Histidine

Histidine is required to make proteins, and the body uses it as the starting material for carnosine (in muscle and parts of the brain) and histamine (in the stomach, immune cells and parts of the brain). [8]
QuestionWhat the source foundLabel
Needed from foodEssential. [8]Established nutritional role
Histidine supplements for any health goalProper evidence not found. We searched PubMed for histidine supplementation reviews; those found concerned carnosine or histidine-containing dipeptides, which are different compounds and are not evidence for histidine itself.Insufficient evidence

Methionine

Methionine is the other building block, with lysine, that the body uses to make carnitine. [9] It is also linked to homocysteine, an amino acid the body normally breaks down quickly using vitamin B12, vitamin B6 and folate; a high level can be a sign that this process is not working right or that B vitamins are lacking. [10] In homocystinuria, an inherited disorder, homocysteine and methionine build up in the blood. [11]

Methionine is not a treatment for high homocysteine; a clinician interprets homocysteine tests and decides on any treatment. Methionine supplements for any health goal: Proper evidence not found in the sources read (searched PubMed for methionine supplementation trials in humans; no systematic review of methionine supplements was read). See methionine, homocysteine and sulfur amino acids and vitamin B12.

Phenylalanine

Phenylalanine is found in all proteins. [2] PKU is an inherited disorder in which the body cannot break phenylalanine down; untreated, it can build up to harmful levels and cause intellectual disability and other serious problems. [2] The PKU diet limits high-protein foods because phenylalanine is in all protein. [2] In the US, the FDA says people with PKU should avoid or restrict aspartame, a sweetener that contains phenylalanine, and that newborns are routinely tested for PKU with a heel-prick test. [12] Full detail is on phenylalanine, PKU and aspartame. Phenylalanine supplements for mood, skin or pain: Proper evidence not found in the sources read.

Threonine

Threonine is on MedlinePlus's list of essential amino acids. [1] Threonine supplements: Proper evidence not found (searched PubMed for threonine supplementation trials in humans; no systematic review was read). Threonine in food generally follows the pattern above: richer in animal products. [5]

Valine

Valine is one of the three branched-chain amino acids and is found in many foods, particularly protein-rich foods such as milk, meat and eggs. [3] A meta-analysis found higher plasma levels of valine, leucine and isoleucine associated with later type 2 diabetes. [13] That is an association with blood levels, not proof that food or supplements cause diabetes. Valine on its own as a supplement: Proper evidence not found; see the BCAA guide for products that contain it with leucine and isoleucine.

Upper limits

No national agency has set upper intake levels for individual amino acids, according to a 2023 review. [14] Under an initiative of a nonprofit amino acid science council, researchers reported these values from clinical studies of relatively healthy adults.
Amino acidResearch estimateNotes
HistidineNo-observed-adverse-effect level 8 g a day; lowest-observed-adverse-effect level 12 g a dayHealthy adults, research estimate [14]
Methionine3.2 g a day and 6.4 g a day (same two measures)Healthy adults, research estimate [14]
PhenylalanineNo-observed-adverse-effect level 12 g a dayHealthy adults, not people with PKU [14]

Threonine and valine were not among the amino acids in that review's value list. These are research estimates, not official limits, not advice and not for people with metabolic disorders or kidney or liver disease.

Product quality, medicines and surgery

Single amino acid products vary in what they contain; see quality testing and certifications. For medicine questions, see medication interactions and amino acid supplements and medicines. Tell the surgical team about every supplement (supplements before surgery).

Frequently asked questions

Which essential amino acids are covered here?

Histidine, methionine, phenylalanine, threonine and valine. The other four have their own pages. [1]

Why is phenylalanine on some sweetener labels?

Aspartame contains phenylalanine, and the FDA says people with PKU should avoid or restrict it. [12]

Is methionine linked to homocysteine?

Homocysteine is an amino acid the body normally breaks down using vitamins B12, B6 and folate, and homocysteine and methionine both build up in the blood in homocystinuria. [10][11]

Do I need histidine, threonine or valine supplements?

Proper evidence not found that they help healthy people who eat enough protein; ask a clinician or dietitian.

Is there an official upper limit for these amino acids?

Not from national health agencies, according to a 2023 review; research estimates exist for some. [14]

More details: evidence, limits and cautions

The details behind this page: cautions, limits of the evidence and where sources disagree. Open any note to read it.

Overview and who should ask first
Histidine, methionine, phenylalanine, threonine and valine are five of the nine essential amino acids: the body cannot make them, so they must come from food. [1] Leucine and isoleucine (with valine, the BCAAs) are in the BCAA guide; tryptophan and lysine have their own pages. The group overview is essential amino acids.

Two inherited conditions make some of these amino acids dangerous in excess, so supplements or diet changes belong with a specialist team: in phenylketonuria (PKU), phenylalanine can build up to harmful levels, [2] and in maple syrup urine disease, valine (with leucine and isoleucine) builds up and is toxic to the brain and other organs. [3] Children, pregnancy, breastfeeding, kidney or liver disease, and prescribed medicines are also reasons to ask a clinician, pharmacist or dietitian before taking any single amino acid product; the sources read gave no supplement-specific guidance for these five (Proper evidence not found).

References
  1. MedlinePlus. Amino acids. National Library of Medicine, US. Review date 1/21/2025. Read 2026-10-22.
  2. MedlinePlus Genetics. Phenylketonuria. National Library of Medicine, US. Read 2026-10-22.
  3. MedlinePlus Genetics. Maple syrup urine disease. National Library of Medicine, US. Read 2026-10-22.
  4. MedlinePlus. Protein in diet. National Library of Medicine, US. Read 2026-10-22.
  5. Li P, He W, Wu G. Composition of amino acids in foodstuffs for humans and animals. Adv Exp Med Biol. 2021. Read 2026-10-22.
  6. Health Canada. Dietary reference intakes tables: Reference values for macronutrients. Government of Canada, page dated 2025-11-19. Read 2026-10-22 through a web-fetch tool that summarised the page; rows as reported by that tool.
  7. Burstad KM et al. Evaluation of dietary protein and amino acid requirements: a systematic review. Am J Clin Nutr. 2025. Read 2026-10-22.
  8. Brosnan ME, Brosnan JT. Histidine metabolism and function. J Nutr. 2020. Read 2026-10-22.
  9. Almannai M et al. Carnitine inborn errors of metabolism. Molecules. 2019. Read 2026-10-22.
  10. MedlinePlus. Homocysteine test. National Library of Medicine, US. Read 2026-10-22.
  11. MedlinePlus Genetics. Homocystinuria. National Library of Medicine, US. Read 2026-10-22.
  12. FDA. Aspartame and Other Sweeteners in Food. US Food and Drug Administration. Read 2026-10-22.
  13. Ramzan I et al. Circulating branched chain amino acids and the temporal risk of type 2 diabetes: systematic review and meta-analysis. Nutrients. 2022. Read 2026-10-22.
  14. Elango R. Tolerable upper intake level for individual amino acids in humans: a narrative review of recent clinical studies. Adv Nutr. 2023. Read 2026-10-22.
Education, not medical advice. This page is for general information. It does not diagnose or treat any condition and is not a substitute for care from a qualified health professional. Natural does not automatically mean safe. Ask a clinician or pharmacist before changing your care, especially if you take medication, are pregnant or breastfeeding, or have a health condition.