Accelerating the peroxidase-like activity of Co2+ by quinaldic acid: Mechanism and its analytical applications

被引:5
|
作者
Xu, Lijun [1 ]
Xue, Dongguo [1 ]
Sai, Jialin [1 ]
Zhou, Lu [2 ]
Pei, Renjun [3 ]
Liu, Aihua [1 ]
机构
[1] Qingdao Univ, Coll Life Sci, Inst Chem Biol & Biosensing, 308 Ningxia Rd, Qingdao 266071, Peoples R China
[2] Tongji Univ, Shanghai Dermatol Hosp, Dept Med Mycol, Shanghai 200443, Peoples R China
[3] Chinese Acad Sci, Key Lab Nanobio Interface, Div Nanobiomed, Suzhou Inst Nanotech & Nanobion, Suzhou 215123, Peoples R China
关键词
Quinaldic acid; Cobalt; Bicarbonate; Peroxidase; Enzyme mimics; Urease; HYDROGEN-PEROXIDE; UREASE ACTIVITY; COLORIMETRIC DETECTION; ORANGE II; CHEMILUMINESCENCE; DEGRADATION; REDUCTION; CATALYST; PLATFORM; ION;
D O I
10.1016/j.talanta.2021.123080
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Although enzyme mimics have been widely developed, limited catalytic efficiency is still a bottleneck, especially under neutral condition. Herein, we reported the bioactive quinaldic acid (QA) significantly boosted the peroxidase-like activity of Co2+ in the presence of bicarbonate (HCO3-). With 2,2 '-azino-bis-(3-ethyl-benzothiazoline-6-sulphonate) (ABTS) as the substrate, the catalytic activity of Co2+ (1 mu M) was increased by over 300 times upon adding 100 mu M QA. The formed Co2+ complex had much higher turnover number (5.52 min(-1)) than that of cobalt-based nanozymes (0.011-0.51 min(-1)) in decomposing H2O2. Based on this system, ultrasensitive colorimetric methods for the detection of Co2+, bicarbonate and urease activity were achieved with limits of detection of 4.6 nM, 40 mu M and 0.00125 U/mL, respectively. For the first time, this work established an ultrasensitive method for the detection of urease activity by activating a peroxidase-like mimic with the pro-duced HCO3-.
引用
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页数:8
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