Follmer Cristian, Real-Guerra Rafael, Wasserman German E, Olivera-Severo Deiber, Carlini Célia R
Department of Biophysics, IB, and Graduate Program in Cellular and Molecular Biology, Center of Biotechnology, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Eur J Biochem. 2004 Apr;271(7):1357-63. doi: 10.1111/j.1432-1033.2004.04046.x.
In this work we compared two plant ureases, jackbean urease (JBU) and embryo-specific soybean urease (SBU) and a bacterial (Bacillus pasteurii) urease, for kinetic parameters and other biological properties described recently for ureases that are independent of the ureolytic activity. The insecticidal effect of ureases was investigated in feeding trials with the cotton sucker bug, Dysdercus peruvianus (Hemiptera) as an insect model. Contrasting with B. pasteurii urease (PBU), both plant ureases presented potent insecticidal activity, with LD(50) values of 0.017% (w/w) and 0.052% (w/w) for JBU and SBU, respectively. The insecticidal property of JBU or SBU was not affected by treatment with p-hydroxymercuribenzoate, an irreversible inhibitor of ureolytic activity of both proteins. Also, contrasting with canatoxin - a urease isoform from jackbean seeds that displays a toxic effect in mice (LD(50) = 2 mg x kg(-1)) - no lethality was seen in mice injected intraperitoneally with JBU or SBU (20 mg x kg(-1)). Similarly to canatoxin, the three enzymes promoted aggregation of blood platelets (EC(50) = 400.0 micro g x mL(-1), 22.2 micro g x mL(-1), 15.8 micro g x mL(-1) for BPU, SBU and JBU, respectively). This platelet activating property was also independent of urease activity. Comparison of the kinetic properties indicated that SBU is fivefold less susceptible than JBU to inhibition by acetohydroxamic acid, a chelator of Ni(+2) and Zn(+2) ions. The ureases also showed different susceptibility to agents that modify cysteine residues, such as p-hydroxymercuribenzoate and p-benzoquinone. Altogether, these data emphasize that biological properties that are independent of ureolytic activity are not restricted to jackbean ureases and that these proteins may have a role in plant defense against insect predators.
在本研究中,我们比较了两种植物脲酶,即刀豆脲酶(JBU)和胚胎特异性大豆脲酶(SBU),以及一种细菌(巴氏芽孢杆菌)脲酶,以研究其动力学参数和最近描述的与尿素分解活性无关的其他生物学特性。以棉蝽(Dysdercus peruvianus,半翅目)为昆虫模型,通过喂食试验研究了脲酶的杀虫效果。与巴氏芽孢杆菌脲酶(PBU)不同,两种植物脲酶均表现出强大的杀虫活性,JBU和SBU的半数致死剂量(LD50)值分别为0.017%(w/w)和0.052%(w/w)。对羟基汞苯甲酸是这两种蛋白质尿素分解活性的不可逆抑制剂,用其处理后,JBU或SBU的杀虫特性不受影响。此外,与刀豆毒素(一种来自刀豆种子的脲酶同工型,对小鼠有毒性作用,LD50 = 2 mg·kg-1)不同,腹腔注射JBU或SBU(20 mg·kg-1)的小鼠未出现致死情况。与刀豆毒素类似,这三种酶均能促进血小板聚集(BPU、SBU和JBU的半数有效浓度(EC50)分别为400.0 μg·mL-1、22.2 μg·mL-1和15.8 μg·mL-1)。这种血小板激活特性也与脲酶活性无关。动力学特性比较表明,SBU对乙酰氧肟酸(一种Ni(+2)和Zn(+2)离子螯合剂)抑制作用的敏感性比JBU低五倍。脲酶对修饰半胱氨酸残基的试剂(如对羟基汞苯甲酸和对苯醌)也表现出不同的敏感性。总之,这些数据强调,与尿素分解活性无关的生物学特性并不局限于刀豆脲酶,这些蛋白质可能在植物抵御昆虫捕食者方面发挥作用。