Cloning and Expression of β-(1,3-1,4) Glucanase (Lichenase) Gene in Bacillus subtilis RSKK246 to create new Probiotic in aquaculture

被引:2
|
作者
Cam, Ozgen A. [1 ]
Baylan, Makbule [2 ]
Mazi, Gamze [2 ]
机构
[1] Cukurova Univ, Dept Basic Sci, Inst Nat & Appl Sci, TR-01330 Adana, Turkey
[2] Cukurova Univ, Fac Fisheries, TR-01330 Adana, Turkey
来源
ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS | 2022年 / 94卷 / 04期
关键词
Bacillus subtilis; ss (1,3-1,4) glucanase; gene transfer; probiotic; ESCHERICHIA-COLI; BETA-GLUCANASE; XYLANASE;
D O I
10.1590/0001-3765202220200913
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ss-Glucan is an essential component of the cell walls of grains such as oats and barley. 1,3-1,4-ss-D-glucan 4-glucanhydrolase (ss-glucanase or lichenase) (EC 3.2.1.73) is an enzyme with the ability to hydrolyze ss-glucans. In this research, ss-Glucan which is a good source of feed additive fish probiotics, was used in order to benefit from feed quality in fishery products, to increase live weight gain and to strengthen the immune system. In this study, recombinant vector pNW33N carrying the ss-(1,3-1,4) glucanase (lichenase) gene of Streptococcus bovis genome was transferred to Bacillus subtilis RSKK246 (CMCase+) strain by electroporation. Subsequently, electrotransformation was performed on LB-agar plates containing lichenan and enzymatic activity regions of recombinant B. subtilis RSKK246 colonies were observed by staining with Congo red. In addition, the DNA from the recombinant plasmid pNW33N+Lichenase (pNW33NLic) was cut on both the BamHI and HindIII endonucleases and observed on the lichenase gene (1800 bp) agarose gel. On the other hand, the protein band corresponding to 26 kDa of the recombinant enzyme was observed by zymogram analysis. These results indicate that the ss-(1,3-1,4) glucanase gene has been successfully expressed to the B. subtilis strain RSKK246.
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页数:8
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