Heumann Sonja, Eberl Anita, Pobeheim Herbert, Liebminger Stefan, Fischer-Colbrie Gudrun, Almansa Eva, Cavaco-Paulo Artur, Gübitz Georg M
Research Centre Applied Biocatalysis, Petersgasse 14, A-8010 Graz, Austria.
J Biochem Biophys Methods. 2006 Nov 30;69(1-2):89-99. doi: 10.1016/j.jbbm.2006.02.005. Epub 2006 Mar 9.
Recently the potential of enzymes for surface hydrophilisation and/or functionalisation of polyethyleneterephthalate (PET) and polyamide (PA) has been discovered. However, there was no correlation between enzyme class/activity (e.g. esterase, lipase, cutinase) and surface hydrolysis of these polymers and consequently no simple assay to estimate this capability. Enzymes active on the model substrates bis (benzoyloxyethyl) terephthalate and adipic acid bishexyl-amide, were also capable of increasing the hydrophilicity of PET and PA. When dosed at the identical activity on 4-nitrophenyl butyrate, only enzymes from Thermobifida fusca, Aspergillus sp., Beauveria sp. and commercial enzymes (TEXAZYME PES sp5 and Lipase PS) increased the hydrophilicity of PET fibres while other esterases and lipases did not show any effect. Activity on PET correlated with the activity on the model substrate. Hydrophilicity of fibres was greatly improved based on increases in rising height of up to 4.3 cm and the relative decrease of water absorption time between control and sample of the water was up to 76%. Similarly, enzymes increasing the hydrophilicity of PA fibres such as from Nocardia sp., Beauveria sp. and F. solani hydrolysed the model substrate; however, there was no common enzyme activity (e.g. protease, esterase, amidase) which could be attributed to all these enzymes.
最近,人们发现了酶在聚对苯二甲酸乙二酯(PET)和聚酰胺(PA)表面亲水化和/或功能化方面的潜力。然而,酶的类别/活性(如酯酶、脂肪酶、角质酶)与这些聚合物的表面水解之间没有相关性,因此也没有简单的方法来评估这种能力。对模型底物对苯二甲酸双(苯甲酰氧基乙酯)和己二酸双己基酰胺有活性的酶,也能够提高PET和PA的亲水性。当以相同活性对4-硝基苯基丁酸进行加样时,只有来自嗜热栖热放线菌、曲霉属、白僵菌属的酶以及商业酶(TEXAZYME PES sp5和脂肪酶PS)能提高PET纤维的亲水性,而其他酯酶和脂肪酶则没有任何效果。对PET的活性与对模型底物的活性相关。基于高达4.3厘米的上升高度增加以及对照与样品之间水吸收时间相对减少高达76%,纤维的亲水性得到了极大改善。同样,能提高PA纤维亲水性的酶,如来自诺卡氏菌属、白僵菌属和茄丝核菌的酶,能水解模型底物;然而,没有一种共同的酶活性(如蛋白酶、酯酶、酰胺酶)可归因于所有这些酶。