Anion inhibitors of the beta-carbonic anhydrase from the pathogenic bacterium responsible of tularemia, Francisella tularensis

作者：Del Prete Sonia; Vullo Daniela; Osman Sameh M; AlOthman Zeid; Donald William A; Winum Jean Yves; Supuran Claudiu T^*; Capasso Clemente^*

来源：Bioorganic & Medicinal Chemistry, 2017, 25(17): 4800-4804.

DOI：10.1016/j.bmc.2017.07.033

• Carbonic anhydrase
• beta-Class
• CA inhibitors
• Anions
• Francisella tularensis
• Tularemia

A beta-class carbonic anhydrase (CA, EC 4.2.1.1) from the pathogenic bacterium Francisella tularensis (Ftu beta CA) was cloned and purified, and the anion inhibition profile was investigated. Based on the measured kinetic parameters for the enzyme catalyzed CO2 hydration reaction (k(cat) of 9.8 x 10(5) s(-1) and a loot/K-M of 8.9 x 10(7) M-1 s(-1)), Ftu beta CA is a highly effective enzyme. The activity of Ftu beta CA was not inhibited by a range of anions that do not typically coordinate Zn(II) effectively, including perchlorate, tetrafluoroborate, and hexafluorophosphate. Surprisingly, some anions which generally complex well with many cations, including Zn(II), also did not effectively inhibit FtuBCA, e.g., fluoride, cyanide, azide, nitrite, bisulphite, sulfate, tellurate, perrhenate, perrhuthenate, and peroxydisulfate. However, the most effective inhibitors were in the range of 90-94 tiM (sulfamide, sulfamic acid, phenylarsonic and phenylboronic acid). N,N-Diethyldithiocarbamate (K-I of 0.31 mM) was a moderately potent inhibitor. As Francisella tularensis is the causative agent of tularemia, the discovery of compounds that can interfere with the life cycle of this pathogen may result in novel opportunities to fight antibiotic drug resistance.

• 出版日期2017-9-1