从肠系膜Leuconostoc NRRL B-640中纯化的葡聚糖酶为单一均相蛋白:非变性Native-PAGE分析

R. K. Purama, A. Goyal
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引用次数: 4

摘要

采用聚乙二醇(PEG-400)分离纯化了Leuconostoc mesenteroides NRRL B-640的胞外葡聚糖酶。在25% (v/v) PEG-400浓度下,葡聚糖蔗糖酶的最大比活性为9.2 U/mg,单步纯化16倍。PEG-400纯化后的酶在SDS-PAGE上显示出多个蛋白条带,其中一个突出的条带对应于180 kDa(12)。然而,同样的PEG-$00分离葡聚糖酶样品在非变性的原生page上分析时显示单一,完整和均匀的条带。这表明右旋蔗糖酶在天然状态下保持单分子形式,只有在加载前加热和含有SDS或2-巯基乙醇时才会在变性条件下呈现多种形式。
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Purified Dextransucrase from Leuconostoc mesenteroides NRRL B-640 Exists as Single Homogeneous Protein: Analysis by Non-denaturing Native-PAGE
The extracellular dextransucrase from Leuconostoc mesenteroides NRRL B-640 was purified using polyethylene glycol (PEG-400) fractionation. A 25% (v/v) PEG-400 concentration gave dextransucrase with maximum specific activity of 9.2 U/mg with 16 fold purification in a single step. The purified enzyme by PEG-400 showed multiple protein bands on SDS-PAGE with one prominent band corresponding to the size 180 kDa (12). However, the same PEG-$00 fractionated dextransucrase samples showed single, intact and homogeneous band when analyzed on non-denaturing native-PAGE. This showed that dextransucrase remains in single molecular form in the native state and shows multiple forms only under denaturing conditions when it is heated before loading and when it contained SDS or 2-mercaptoethanol.
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