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Rapid screening of starter cultures for maari based on antifungal properties

机译:基于抗真菌性能的Maari STARTER培养的快速筛选

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Forty Bacillus isolates obtained from maari (used as condiment in Burkina Faso) including 17 B. subtilis, 4 B. circulans, 7 B. pumilus and 6 B. licheniformis were investigated for use as starter cultures in maari production. The isolates were screened by PCR for the sfp gene responsible for the production of the lipopeptide biosurfactant, surfactin. The sfp gene was detected in all of the seventeen B. subtilis isolates, in 2 out of 7 B. pumilus, in 4 out of 6 B. licheniformis whereas no B. circulans was positive for the sfp gene by PCR screening. Furthermore, all the 40 Bacillus spp. were screened for biosurfactant production and inhibitory activity against Aspergillus flavus, A. niger, A. versicolor and Rhizopus oryzae. Results demonstrated a relationship between the presence of the sfp gene and the antifungal activity and biosurfactant production of Bacillus isolates. In addition, molecular typing of the 17 B. subtilis isolates by Multilocus Sequence Typing (MLST) resulted in 15 Sequence Types, one of them included three strains. Randomly Amplified Polymorphic DNA-PCR (RAPD-PCR), used for B. licheniformis, B. megaterium, B. circulans and B. pumilus revealed that the inhibitory activity and biosurfactant production were strain-dependent. Finally, the detection of chitinase (chi) and beta-glucanase (glu) biosynthesis genes was found to be associated with the antifungal activity for 16 B. subtilis isolates. The present work provides a greater understanding of the antifungal activity and biosurfactant production ability within the Bacillus spp. isolated from maari and contributes to the selection of Bacillus isolates to be used as starter cultures for controlled production of maari.
机译:从Maari获得的四十芽孢杆菌(在Burkina Faso中用作调味品),其中包括17 b.枯草芽孢杆菌,4b.Cirulans,7 b.Pumilus和6 B.Hiheniformis被研究用作Maari生产中的起始培养物。通过PCR筛选分离株,用于负责生产脂肽生物活性剂,SUSFACTIN的SFP基因。在7 b. b.pmulilus中的所有17个枯草芽孢杆菌中检测到SFP基因。在6 b中的4例中,在6 b.的4中,嗜睡,而No B.循环对SFP基因的PCR筛选是阳性的。此外,所有40个Bacillus SPP。针对生物活性剂的生产和抑制活性筛选,反对曲霉,A.尼日尔,A. versicolor和Rhizopus Oryzae。结果证明了SFP基因存在与抗真菌活性和生物素活性剂的存在之间的关系。另外,通过多点序列键入(MLST)的17 b.枯草芽孢杆菌分离株的分子键入导致15种序列类型,其中一个株包括三种菌株。随机扩增的多晶型DNA-PCR(RAPD-PCR),用于B.Licheniformis,B. Megutium,B.Cirulans和B.Pumilus揭示了抑制活性和生物活性剂的产生是依赖于应变的。最后,发现丁质酶(Chi)和β-葡聚糖酶(Glu)生物合成基因的检测与16 b.枯草芽孢杆菌分离株的抗真菌活性有关。本作者对芽孢杆菌内的抗真菌活性和生物活性剂的生产能力提供了更大了解。与Maari隔离,有助于选择芽孢杆菌的选择,以用作玛格氏的受控生产的起动器培养物。

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