首页> 外文期刊>Acta biomaterialia >Encapsulation of alpha-amylase into starch-based biomaterials: an enzymatic approach to tailor their degradation rate.
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Encapsulation of alpha-amylase into starch-based biomaterials: an enzymatic approach to tailor their degradation rate.

机译:将α-淀粉酶封装到淀粉基生物材料中:一种酶解方法,可调节其降解速率。

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This paper reports the effect of alpha-amylase encapsulation on the degradation rate of a starch-based biomaterial. The encapsulation method consisted in mixing a thermostable alpha-amylase with a blend of corn starch and polycaprolactone (SPCL), which were processed by compression moulding to produce circular disks. The presence of water was avoided to keep the water activity low and consequently to minimize the enzyme activity during the encapsulation process. No degradation of the starch matrix occurred during processing and storage (the encapsulated enzyme remained inactive due to the absence of water), since no significant amount of reducing sugars was detected in solution. After the encapsulation process, the released enzyme activity from the SPCL disks after 28days was found to be 40% comparatively to the free enzyme (unprocessed). Degradation studies on SPCL disks, with alpha-amylase encapsulated or free in solution, showed no significant differences on the degradation behaviour between both conditions. This indicates that alpha-amylase enzyme was successfully encapsulated with almost full retention of its enzymatic activity and the encapsulation of alpha-amylase clearly accelerates the degradation rate of the SPCL disks, when compared with the enzyme-free disks. The results obtained in this work show that degradation kinetics of the starch polymer can be controlled by the amount of encapsulated alpha-amylase into the matrix.
机译:本文报道了α-淀粉酶包封对淀粉基生物材料降解速率的影响。封装方法包括将热稳定的α-淀粉酶与玉米淀粉和聚己内酯(SPCL)的混合物混合,然后将它们通过压缩成型加工成圆盘。避免了水的存在,以保持较低的水活度,从而在封装过程中使酶的活度最小化。由于在溶液中未检测到大量的还原糖,因此在加工和储存过程中没有发生淀粉基质的降解(由于水的存在,被包封的酶保持无活性)。包封过程后,发现28天后从SPCL圆盘释放的酶活性相对于游离酶(未加工)为40%。在SPCL圆盘上进行的降解研究表明,α-淀粉酶被封装或在溶液中游离,这两种条件之间的降解行为均无显着差异。这表明与无酶盘相比,α-淀粉酶已被成功封装,几乎完全保留了其酶活性,而α-淀粉酶的封装明显加快了SPCL盘的降解速度。在这项工作中获得的结果表明,淀粉聚合物的降解动力学可以通过包裹在基质中的α-淀粉酶的量来控制。

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