Skip to main content
. 2016 Jun 13;82(13):3846–3856. doi: 10.1128/AEM.00665-16

TABLE 1.

Specific and relative activities for a range of amine donors and acceptors

Substrate category and namea Sp act (nmol/min/mg) Relative activityb (%)
Amine donors
    ω-Aminoalkanoates
        Glycine 9.9 ± 2.4 1.4
        β-Alanine 378.3 ± 7.4 54.1
        4-Aminobutyric acid 635.4 ± 9.9 90.8
        5-Aminopentanoic acid 368.4 ± 1.9 52.7
        6-Aminohexanoic acid 437.6 ± 1.3 62.5
        7-Aminoheptanoic acid 482.1 ± 2.5 68.9
        8-Aminooctanoic acid 699.7 ± 9.9 100.0
        12-Aminododecanoic acid 126.1 ± 2.5 18.0
    Diamines
        1,3-Diaminopropane 24.7 ± 0.7 3.5
        Putrescine 267.0 ± 1.7 38.2
        Cadaverine 603.0 ± 0.8 86.2
        1,6-Hexamethylenediamine 388.2 ± 1.7 55.5
        1,7-Heptanediamine 346.2 ± 2.5 49.5
        1,8-Octaneamine 279.4 ± 2.5 39.9
        1,9-Nonanediamine 212.6 ± 2.5 30.4
        1,10-Decanediamine 679.9 ± 7.4 97.2
    Amino acids
        l-Ornithine 4.9 ± 0.3 0.7
        d-Ornithine 27.2 ± 0.3 3.9
        l-Lysine 2.5 ± 0.2 0.4
        d-Lysine 61.8 ± 0.4 8.8
        l-Arginine 4.9 ± 0.4 0.7
        d-Arginine NDc ND
        l-Glutamic acid ND ND
        Citrulline ND ND
    Other amine donors
        N-Acetyl-l-Ornithine ND ND
        4-Amino-2-(S)-hydroxybutyric acid 336.3 ± 2.5 48.1
        5-Aminolevulinic acid ND ND
        Serinol 9.9 ± 0.2 1.4
        d/l-Aminoisobutyric acid 435.2 ± 2.5 62.2
        Taurine 7.4 ± 0.5 1.1
        Creatine ND ND
        3-Aminocyclohexanoic acid 12.4 ± 0.7 1.8
        3-Aminoheptanoic acid 2.5 ± 0.5 0.4
        (S)-2,4-Diaminobutyric acid ND ND
        β-Homoleucine ND ND
        2,6-Diaminopimelate ND ND
        Aminomethylphosphonic acid ND ND
        2-Aminoindane 24.7 ± 0.6 3.5
        2-Methylbenzylamine 54.4 ± 4.9 7.8
        Isopropylamine 232.4 ± 1.3 33.2
        Cyclohexylamine 42.0 ± 0.4 6.0
        6-Aminohexanol 489.6 ± 2.4 70.0
Amine acceptors
    Propionaldehyde 202.0 ± 7.2 68.3
    Butyraldehyde 295.8 ± 7.2 100.0
    Heptanal 21.6 ± 1.8 7.3
    Octanal 24.1 ± 2.1 8.1
    Dodecanal 40.9 ± 19.2 13.8
    Glyceraldehyde 101.0 ± 2.4 34.1
    Cyclohexanone ND ND
    HMF 40.9 ± 1.1 13.8
a

For each amine donor substrate, the acceptor used was pyruvate (assay conditions included potassium phosphate buffer at 100 mM, pH 10). For each amine acceptor substrate, the donor used was L-alanine (assay conditions included potassium phosphate buffer at 100 mM, pH 8).

b

Relative activities are in comparison with 8-aminooctanoic acid for the various amine donors and with butyraldehyde for the amine acceptors.

c

ND, activity not determined.