Fernandez-Lafuente R, Rosell C M, Rodriguez V, Santana C, Soler G, Bastida A, Guisán J M
Unidad de Biocatálisis, Instituto de Catálisis, C.S.I.C. Universidad Autónoma Cantoblanco, Madrid, Spain.
Enzyme Microb Technol. 1993 Jul;15(7):546-50. doi: 10.1016/0141-0229(93)90016-u.
A method for the preparation of new aminated agarose gels containing monoaminoethyl-N-aminoethyl structures, MANA-agarose gels, has been developed. These gels contain primary amino groups with a very low pK value (6.8). In addition to that, we have been able to prepare very highly activated gels (e.g., 10% agarose gels containing up to 200 mu Eq of primary amines per milliliter). These two properties make these activated supports suitable for performing novel and interesting methods for protein immobilizations via very mild carbodiimide activation of carboxy groups. For example, very effective coupling reactions can be performed at pH 5.0-6.0 in the presence of low concentrations of activating agent, e.g., 1 mM. By using a model industrial enzyme, beta-galactosidase from Aspergillus oryzae, we have been able to demonstrate the excellent prospects of these novel activated supports.
已开发出一种制备含有单氨基乙基 - N - 氨基乙基结构的新型胺化琼脂糖凝胶(MANA - 琼脂糖凝胶)的方法。这些凝胶含有pK值非常低(6.8)的伯氨基。此外,我们还能够制备活性非常高的凝胶(例如,10%的琼脂糖凝胶,每毫升含有高达200μEq的伯胺)。这两个特性使得这些活性载体适用于通过非常温和的羧基碳二亚胺活化来进行蛋白质固定的新颖有趣的方法。例如,在低浓度活化剂(如1 mM)存在下,可在pH 5.0 - 6.0进行非常有效的偶联反应。通过使用一种典型的工业酶——米曲霉β - 半乳糖苷酶,我们已经能够证明这些新型活性载体的优异前景。