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Sequencing of Spodoptera frugiperda midgut trehalases and demonstration of secretion of soluble trehalase by midgut columnar cells

机译:草地贪夜蛾中肠海藻糖酶的测序及中肠柱状细胞分泌可溶性海藻糖酶的证明

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摘要

Both soluble (SfTre1) and membrane-bound (SfTre2) trehalases occur along the midgut of Spodoptera frugiperda larvae. Released SfTre2 was purified as a 67 kDa protein. Its Km (1.6 mM) and thermal stability (half life 10 min at 62 pC) are different from the previously isolated soluble trehalase (Km= 0.47 mM; 100% stable at 62 pC). Two cDNAs coding for S. frugiperda trehalases have been cloned using primers based on consensus sequences of trehalases and having as templates a cDNA library prepared from total polyA-containing RNA extracted from midguts. One cDNA codes for a trehalase that has a predicted transmembrane sequence and was defined as SfTre2. The other, after being cloned and expressed, results in a recombinant trehalase with a Km value and thermal stability like those of native soluble trehalase. This enzyme was defined as SfTre1 and, after it was used to generate antibodies, it was immunolocalized at the secretory vesicles and at the glycocalyx of columnar cells. Escherichia coli trehalase 3D structure and sequence alignment with SfTre1 support a proposal regarding the residue modulating the pKa value of the proton donor.
机译:可溶性(SfTre1)和膜结合(SfTre2)海藻糖酶都沿着斜纹夜蛾幼虫的中肠发生。将释放的SfTre2纯化为67 kDa蛋白。它的Km(1.6 mM)和热稳定性(在62 pC时的半衰期为10分钟)不同于先前分离的可溶性海藻糖酶(Km = 0.47 mM;在62 pC时100%稳定)。使用基于海藻糖酶共有序列的引物已克隆了两个编码节肢链球菌海藻糖酶的cDNA,并具有一个模板,该文库由从中肠提取的总含polyA的RNA制备而成。一种cDNA编码的海藻糖酶具有预测的跨膜序列,被定义为SfTre2。另一个在克隆和表达后,产生的重组海藻糖酶具有Km值和热稳定性,就像天然可溶性海藻糖酶一样。将该酶定义为SfTre1,并用于产生抗体后,将其免疫定位在分泌小泡和柱状细胞的糖萼上。大肠杆菌海藻糖酶3D结构和与SfTre1的序列比对支持有关调节质子供体pKa值的残基的提议。

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