Hooks David O, Venning-Slater Mark, Du Jinping, Rehm Bernd H A
Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand.
Molecules. 2014 Jun 24;19(6):8629-43. doi: 10.3390/molecules19068629.
Polyhydroxyalkanoate (PHA) is a carbon storage polymer produced by certain bacteria in unbalanced nutrient conditions. The PHA forms spherical inclusions surrounded by granule associate proteins including the PHA synthase (PhaC). Recently, the intracellular formation of PHA granules with covalently attached synthase from Ralstonia eutropha has been exploited as a novel strategy for oriented enzyme immobilisation. Fusing the enzyme of interest to PHA synthase results in a bifunctional protein able to produce PHA granules and immobilise the active enzyme of choice to the granule surface. Functionalised PHA granules can be isolated from the bacterial hosts, such as Escherichia coli, and maintain enzymatic activity in a wide variety of assay conditions. This approach to oriented enzyme immobilisation has produced higher enzyme activities and product levels than non-oriented immobilisation techniques such as protein inclusion based particles. Here, enzyme immobilisation via PHA synthase fusion is reviewed in terms of the genetic designs, the choices of enzymes, the control of enzyme orientations, as well as their current and potential applications.
聚羟基脂肪酸酯(PHA)是某些细菌在营养不均衡条件下产生的一种碳储存聚合物。PHA形成球形内含物,被包括PHA合酶(PhaC)在内的颗粒相关蛋白包围。最近,利用来自真养产碱菌的具有共价连接合酶的PHA颗粒在细胞内的形成作为一种定向酶固定化的新策略。将感兴趣的酶与PHA合酶融合会产生一种双功能蛋白,该蛋白能够产生PHA颗粒并将所选的活性酶固定在颗粒表面。功能化的PHA颗粒可以从细菌宿主(如大肠杆菌)中分离出来,并在各种测定条件下保持酶活性。与基于蛋白质包涵体颗粒等非定向固定化技术相比,这种定向酶固定化方法产生了更高的酶活性和产物水平。在此,从基因设计、酶的选择、酶取向的控制以及它们当前和潜在的应用等方面对通过PHA合酶融合进行的酶固定化进行综述。