Activation studies with amino acids and amines of a β-carbonic anhydrase from Mammaliicoccus (Staphylococcus) sciuri previously annotated as Staphylococcus aureus (SauBCA) carbonic anhydrase

被引:10
作者
Angeli, Andrea [1 ]
Urbanski, Linda J. [2 ]
Capasso, Clemente [3 ]
Parkkila, Seppo [2 ,4 ]
Supuran, Claudiu T. [1 ]
机构
[1] Univ Firenze, Sez Sci Farmaceut & Nutraceut, Dipartimento Neurofarba, Sesto Fiorentino, Florence, Italy
[2] Tampere Univ, Fac Med & Hlth Technol, Tampere, Finland
[3] Inst Biosci & Bioresources, Dept Biol Agr & Food Sci, Naples, Italy
[4] Tampere Univ Hosp, Fimlab Ltd, Tampere, Finland
基金
芬兰科学院;
关键词
Staphylococcaceae; carbonic anhydrase; activator; amine; amino acid; Mammaliicoccus (Staphylococcus) sciuri; HISTAMINE SCHIFF-BASES; ISOZYME-II; ACTIVE-SITE; CRYSTAL-STRUCTURE; ESCHERICHIA-COLI; SPECTROSCOPIC INVESTIGATIONS; CRYSTALLOGRAPHIC ANALYSIS; PATHOGENIC BACTERIA; ISOFORM-VII; L-HISTIDINE;
D O I
10.1080/14756366.2022.2131780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A beta-carbonic anhydrase (CA, EC 4.2.1.1) previously annotated to be present in the genome of Staphylococcus aureus, SauBCA, has been shown to belong to another pathogenic bacterium, Mammaliicoccus (Staphylococcus) sciuri. This enzyme, MscCA, has been investigated for its activation with a series of natural and synthetic amino acid and amines, comparing the results with those obtained for the ortholog enzyme from Escherichia coli, EcoCA beta. The best MscCA activators were D-His, L- and D-DOPA, 4-(2-aminoethyl)-morpholine and L-Asn, which showed K(A)s of 0.12 - 0.89 mu M. The least efficient activators were D-Tyr and L-Gln (K(A)s of 13.9 - 28.6 mu M). The enzyme was also also inhibited by anions and sulphonamides, as described earlier. Endogenous CA activators may play a role in bacterial virulence and colonisation of the host which makes this research topic of great interest.
引用
收藏
页码:2786 / 2792
页数:7
相关论文
共 96 条
[1]   Application of the dual-tail approach for the design and synthesis of novel Thiopyrimidine-Benzenesulfonamide hybrids as selective carbonic anhydrase inhibitors [J].
Abdel-Mohsen, Heba T. ;
El Kerdawy, Ahmed M. ;
Omar, Mohamed A. ;
Petreni, Andrea ;
Allam, Rasha M. ;
El Diwani, Hoda, I ;
Supuran, Claudiu T. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2022, 228
[2]   Repurposing FDA-approved sulphonamide carbonic anhydrase inhibitors for treatment of Neisseria gonorrhoeae [J].
Abutaleb, Nader S. ;
Elhassanny, Ahmed E. M. ;
Nocentini, Alessio ;
Hewitt, Chad S. ;
Elkashif, Ahmed ;
Cooper, Bruce R. ;
Supuran, Claudiu T. ;
Seleem, Mohamed N. ;
Flaherty, Daniel P. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2022, 37 (01) :51-61
[3]   Activation of α-, β-, γ- δ-, ζ- and η- class of carbonic anhydrases with amines and amino acids: a review [J].
Akocak, Suleyman ;
Supuran, Claudiu T. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2019, 34 (01) :1652-1659
[4]   Activation of human α-carbonic anhydrase isoforms I, II, IV and VII with bis-histamine schiff bases and bis-spinaceamine substituted derivatives [J].
Akocak, Suleyman ;
Lolak, Nabih ;
Bua, Silvia ;
Nocentini, Alessio ;
Supuran, Claudiu T. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2019, 34 (01) :1193-1198
[5]   α-Carbonic anhydrases are strongly activated by spinaceamine derivatives [J].
Akocak, Suleyman ;
Lolak, Nabih ;
Bua, Silvia ;
Nocentini, Alessio ;
Karakoc, Gulcin ;
Supuran, Claudiu T. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2019, 27 (05) :800-804
[6]   Synthesis and biological evaluation of histamine Schiff bases as carbonic anhydrase I, II, IV, VII, and IX activators [J].
Akocak, Suleyman ;
Lolak, Nabih ;
Vullo, Daniela ;
Durgun, Mustafa ;
Supuran, Claudiu T. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2017, 32 (01) :1305-1312
[7]   Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms? [J].
Alterio, Vincenzo ;
Di Fiore, Anna ;
D'Ambrosio, Katia ;
Supuran, Claudiu T. ;
De Simone, Giuseppina .
CHEMICAL REVIEWS, 2012, 112 (08) :4421-4468
[8]  
Amedei Amedeo, 2021, Mediators Inflamm, V2021, P6926082, DOI 10.1155/2021/6926082
[9]   Structure-activity relationship studies for inhibitors for vancomycin-resistant Enterococcus and human carbonic anhydrases [J].
An, Weiwei ;
Holly, Katrina J. ;
Nocentini, Alessio ;
Imhoff, Ryan D. ;
Hewitt, Chad. S. ;
Abutaleb, Nader S. ;
Cao, Xufeng ;
Seleem, Mohamed N. ;
Supuran, Claudiu T. ;
Flaherty, Daniel P. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2022, 37 (01) :1838-1844
[10]   The first activation study of the β-carbonic anhydrases from the pathogenic bacteria Brucella suis and Francisella tularensis with amines and amino acids [J].
Angeli, Andrea ;
Del Prete, Sonia ;
Pinteala, Mariana ;
Maier, Stelian S. ;
Donald, William A. ;
Simionescu, Bogdan C. ;
Capasso, Clemente ;
Supuran, Claudiu T. .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2019, 34 (01) :1178-1185