Enzymatic hydrolysis of molecules associated with bacterial quorum sensing using an acyl homoserine lactonase from a novel Bacillus thuringiensis strain

Antonie van Leeuwenhoek, International Journal of General and Molecular Microbiology

Volumn 105, Issue 1, 2014, Pages 253-264

  Pedroza, Carmen Julia ^b   Flórez, Alvaro Mauricio ^a   Ruiz, Orlando S ^b   Orduz, Sergio ^b  

^a UNIVERSIDAD DE SANTANDER   (Colombia)

^b UNIVERSIDAD NACIONAL DE COLOMBIA   (Colombia)

Author keywords

AHL lactonase; N acyl homoserine lactone; Quorum quenching; Quorum sensing

Indexed keywords

ACYL HOMOSERINE LACTONASE; EDETIC ACID; GLUCONOLACTONASE; METAL ION; RECOMBINANT ENZYME; UNCLASSIFIED DRUG;

ARTICLE; BACILLUS THURINGIENSIS; BACTERIAL STRAIN; CONCENTRATION RESPONSE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME KINETICS; ENZYME SPECIFICITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; MASS SPECTROMETRY; NONHUMAN; NUCLEOTIDE SEQUENCE; PH; PRIORITY JOURNAL; QUORUM SENSING; TEMPERATURE;

BACILLUS THURINGIENSIS; BACTERIA (MICROORGANISMS); NEGIBACTERIA;

4-BUTYROLACTONE; BACILLUS THURINGIENSIS; BACTERIAL PROTEINS; CARBOXYLIC ESTER HYDROLASES; ENZYME STABILITY; HYDROLYSIS; KINETICS; MOLECULAR STRUCTURE; QUORUM SENSING; SUBSTRATE SPECIFICITY;

EID: 84892819712     PISSN: 00036072     EISSN: 15729699     Source Type: Journal    
DOI: 10.1007/s10482-013-0072-5     Document Type: Article

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