Bioengineered protein phosphatase 2A Update on need

被引:1
|
作者
Rubiolo, Juan A. [1 ]
Lopez-Alonso, Henar [2 ]
Alfonso, Amparo [2 ]
Vega, Felix V. [1 ]
Vieytes, Mercedes Rodriguez [1 ]
Botana, Luis M. [2 ]
机构
[1] Fac Vet, Dept Fisiol, Lugo, Spain
[2] Fac Vet, Dept Farmacol, Lugo, Spain
关键词
recombinant PP2AC; insect larvae; harmful algal blooms; eutrophication; natural toxin detection; CATALYTIC SUBUNIT-ALPHA; HARMFUL ALGAL BLOOMS; OKADAIC ACID; FUNCTIONAL EXPRESSION; INHIBITION ASSAY; POTENT INHIBITOR; IDENTIFICATION; HEALTH; PURIFICATION; CLIMATE;
D O I
10.4161/bioe.22461
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Harmful algal blooms caused by phytoplankton can occur in all aquatic environments. Some of the algae present in these blooms are capable of producing extremely potent toxins. Due to climate change and eutrophication, harmful algal blooms are increasing on a global scale. One kind of toxin producing algae are those that produce okadaic acid, its derivatives (dinophysistoxin-1 and 2), and microcystins. These toxins are potent inhibitors of protein phosphatase 2A, so this protein is used to detect the mentioned toxins in natural samples. Originally protein phosphatase 2A purified from animal tissues was used, but enzyme activity and stability fluctuations prevented the use of the enzyme in detection kits. Expression of the enzyme as a recombinant protein provided a solution to this problem. For this purpose, several strategies have been followed. We evaluated the activity, specificity and stability of the human protein phosphatase 2A catalytic subunit a expressed in insect larvae and showed that this expression system can be a reliable source of high quantities of stable enzyme.
引用
收藏
页码:72 / 77
页数:6
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