Component

Intestinal PLP hydrolysis

Dephosphorylation of luminal PLP.

2 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. Rat jejunal perfusion and in-vitro assays demonstrated phosphatase-mediated hydrolysis of luminal PLP.

    Intestinal PLP hydrolysis → Pyridoxal source_derived_draftungraded
    Experimental context and source evidence
    evidence_location
    Indexed abstract: hydrolysis, albumin and pH experiments
    experimental_model
    Rat jejunal perfusion and in-vitro phosphatase assays.
    exposure
    PLP hydrolysis tested across luminal pH and albumin concentrations.
    limitations
    Luminal disappearance is not a complete absorption balance; no specific human phosphatase is assigned.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Rattus norvegicus
    plain_language
    Intestinal phosphatases remove PLP phosphate.
    primary_references
    [middleton1986] Intestinal hydrolysis of pyridoxal 5'-phosphate in vitro and in vivo in the rat. Effect of protein binding and pH. (1986). https://pubmed.ncbi.nlm.nih.gov/3721120/ DOI: 10.1016/0016-5085(86)90567-6
    tissue_or_cell_type
    Jejunum

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 72–83

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Rat jejunal perfusion and in-vitro phosphatase assays. · source_derived_draft · unverified_draft

    ### b6-transport-gut-plp-hydrolysis Rat jejunal perfusion and in-vitro assays demonstrated phosphatase-mediated hydrolysis of luminal PLP. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Intestinal phosphatases remove PLP phosphate. organism: Rattus norvegicus tissue_or_cell_type: Jejunum experimental_model: Rat jejunal perfusion and in-vitro phosphatase assays. limitations: Luminal disappearance is not a complete absorption balance; no specific human phosphatase is assigned. exposure: PLP hydrolysis tested across luminal pH and albumin concentrations. evidence_location: Indexed abstract: hydrolysis, albumin and pH experiments [middleton1986] Intestinal hydrolysis of pyridoxal 5'-phosphate in vitro and in vivo in the rat. Effect of protein binding and pH. (1986). https://pubmed.ncbi.nlm.nih.gov/3721120/ DOI: 10.1016/0016-5085(86)90567-6
    Complete structured claim and evidence

What acts on it

  1. Albumin binding inhibited hydrolysis of 2 micromolar PLP at pH 5-7.4; at pH 3-4 binding was negligible and hydrolysis persisted.

    PLP → Intestinal PLP hydrolysis source_derived_draftungraded
    Experimental context and source evidence
    evidence_location
    Indexed abstract: hydrolysis, albumin and pH experiments
    experimental_model
    Rat jejunal perfusion and in-vitro phosphatase assays.
    exposure
    2 micromolar PLP, albumin and pH manipulation.
    limitations
    Albumin species is not assigned from the indexed abstract; no human acid-suppression outcome was measured.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Rattus norvegicus
    plain_language
    Protein binding and acidity changed substrate access.
    primary_references
    [middleton1986] Intestinal hydrolysis of pyridoxal 5'-phosphate in vitro and in vivo in the rat. Effect of protein binding and pH. (1986). https://pubmed.ncbi.nlm.nih.gov/3721120/ DOI: 10.1016/0016-5085(86)90567-6
    tissue_or_cell_type
    Perfused jejunum and in-vitro preparations

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 85–96

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Rat jejunal perfusion and in-vitro phosphatase assays. · source_derived_draft · unverified_draft

    ### b6-transport-albumin-gut-hydrolysis Albumin binding inhibited hydrolysis of 2 micromolar PLP at pH 5-7.4; at pH 3-4 binding was negligible and hydrolysis persisted. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Protein binding and acidity changed substrate access. organism: Rattus norvegicus tissue_or_cell_type: Perfused jejunum and in-vitro preparations experimental_model: Rat jejunal perfusion and in-vitro phosphatase assays. limitations: Albumin species is not assigned from the indexed abstract; no human acid-suppression outcome was measured. exposure: 2 micromolar PLP, albumin and pH manipulation. evidence_location: Indexed abstract: hydrolysis, albumin and pH experiments [middleton1986] Intestinal hydrolysis of pyridoxal 5'-phosphate in vitro and in vivo in the rat. Effect of protein binding and pH. (1986). https://pubmed.ncbi.nlm.nih.gov/3721120/ DOI: 10.1016/0016-5085(86)90567-6
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards