Production and characterization of collagenase from a new Amazonian Bacillus cereus strain

被引:11
|
作者
Pequeno, Alexsandra C. L. [1 ]
Arruda, Aline A. [2 ]
Silva, Douglas F. [1 ]
Duarte Neto, Jose M. W. [2 ]
Silveira Filho, Vladimir M. [1 ]
Converti, Attilio [3 ]
Marques, Daniela A. V. [4 ]
Porto, Ana L. F. [5 ]
Lima, Carolina A. [1 ]
机构
[1] Univ Pernambuco UPE, Lab Biotechnol & Therapeut Innovat, Garanhuns, PE, Brazil
[2] Fed Univ Pernambuco UFPE, LIKA, Recife, PE, Brazil
[3] Genoa Univ, Dept Civil Chem & Environm Engn, Genoa, Italy
[4] Univ Pernambuco UPE, Lab Microbiol & Parasitol, Serra Talhada, PE, Brazil
[5] Fed Rural Univ Pernambuco UFRPE, Dept Morphol & Anim Physiol, Recife, PE, Brazil
来源
关键词
Amazon; bacteria; collagenolytic protease; culture conditions; medium; response surface methodology; COLLAGENOLYTIC SERINE-PROTEASE; ALKALINE PROTEASE; PURIFICATION; ENZYMES; FERMENTATION; OPTIMIZATION; SPECIFICITY; PROTEINS; SCAR;
D O I
10.1080/10826068.2019.1587627
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new collagenase producing a strain of Bacillus cereus, isolated from the pollen of a bee of Amazon Region (Brazil), had its enzyme characterized and the production medium composition and culture conditions enhanced. A two-level design on three factors, namely initial medium pH, the substrate (gelatin) concentration and agitation intensity, allowed identifying the first two variables as the most significant ones, while a central composite design (CCD) was subsequently used to identify their optimal levels. Statistics highlighted maximized collagenolytic activity when substrate concentration and initial medium pH were selected at their highest levels (positive effects), whereas agitation intensity at the lowest (negative effect). Triplicate runs performed under predicted optimal conditions (pH 7.8 and 1.7% gelatin concentration) yielded a collagenolytic activity (305.39 +/- 5.15 U) 4.6- to 15-fold those obtained with the preliminary design. The enzyme displayed optimum activity at 45 degrees C and pH 7.2, was stable over wide ranges of pH values and temperatures (7.2-11.0 and 25-50 degrees C, respectively) and was strongly inhibited by 10 mM phenylmethylsulphonyl fluoride. The zymogram showed two prominent bands at 50 and 76 kDa. These results are a first attempt to elucidate the features of this new collagenase, its production conditions, and possible scale-up.
引用
收藏
页码:501 / 509
页数:9
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