1、
确定了其最佳培养基: 蔗糖3%, NaNO_30.2%, K_2HPO_40.1%, MgSO_ 4·7H_2O0.05%, FeSO_40.001%, KCl0.05%.
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2、
Additionally , the mechanism of secretion of HPO was determined.
这就提示我们, HPO可能同这些蛋白类似,具有其独特的分泌机制.
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3、
The method to examine the receptor-binding activity of HPO by FACS was established.
首先构建、表达了HPO及其系列缺失体,建立了利用FACS分析HPO受体结合活性的体外检测方法.
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4、
HPO could transfer the disulfide directly to TRX in vitro and oxidized TRX in vivo.
在体外,二者之间存在直接的二硫键的交换,在体内,HPO可以将TRX氧化.
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