摘要
Based on the specific affinity behavior of teicoplanin towards Gram-positive (G + ) bacteria, teicoplanin-coated magnetic particles were employed to separate G + bacteria. Moreover, intracellular catalase released by catalase-positive bacteria led to catalyzed hydrolysis of H 2 O 2 and inhibition of chemiluminescent signal of luminol-H 2 O 2 system. By combining the separation capability of teicoplanin-coated magnetic particles and the inhibition of luminol chemiluminescence by catalase, a facile method was proposed for quantifying catalase-positive G + bacteria. In this proof-of-principle work, Staphylococcus aureus , Bacillus subtilis and Micrococcus luteus were adopted as model bacteria to evaluate its quantification performance. The three bacteria were quantified within the dynamic ranges of 5.0 × 10 2 –5.0 × 10 7 CFU mL −1 , 4.0 × 10 2 –4.0 × 10 7 CFU mL −1 and 2.0 × 10 2 –2.0 × 10 7 CFU mL −1 , with detection limits of 156 CFU mL −1 , 86 CFU mL −1 and 44 CFU mL −1 , respectively. Gram-negative bacteria and catalase-negative G + bacteria both displayed minor interference. The results for quantifying bacteria in milk, human urine and physiological saline samples demonstrated its reliability for real application. It provided a promising technique tool for food safety, medical diagnosis as well as drug quality control.
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