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Investigation of the diversity and safety of the predominant Bacillus pumilus sensu lato and other Bacillus species involved in the alkaline fermentation of cassava leaves for the production of Ntoba Mbodi

机译:木薯叶片碱性发酵过程中主要的短小芽孢杆菌和其他芽孢杆菌物种的多样性和安全性研究,用于生产Ntoba Mbodi

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摘要

The objective of the study was to investigate the identity, diversity, and safety of the Bacillus population involved in the fermentation of cassava (Manihot esculenta Crantz) leaves for the production of Ntoba Mbodi, a Congolese food. Ninety bacteria were identified by phenotyping and genotyping using ITS-PCR, rep-PCR, and sequencing of the 16S rRNA, gyrA, gyrB and rpoB genes. Moreover, the isolates were screened for the presence of genes coding for haemolytic (HblC, HblD) and non-haemolytic enterotoxins (NheA, NheB and NheC), cytotoxin K (CytK) and emetic toxin (EM1) as well as their ability to produce haemolysin.The investigations revealed the predominance (72.21 %) of species of the Bacillus pumilus group i.e. B. safensis (48), B. pumilus (7), and B. pumilus sensu lato (10). Other species of Bacillus including B. cereus sensu lato (11), B. megaterium (4), B. subtilis (4), B. amyloliquefaciens (2), B. siamensis (2), B. licheniformis (1) and Lysinibacillus louembei were also identified. Haemolytic, non-haemolytic and cytokin toxin genes were detected in the B. cereus strains which were also able to produce haemolysin. The emetic toxin gene was not detected in any isolates. The toxin genes screened were not detected in any of the non B. cereus species.
机译:这项研究的目的是调查参与木薯(Manihot esculenta Crantz)叶片发酵的芽孢杆菌种群的身份,多样性和安全性,以生产刚果粮食Ntoba Mbodi。使用ITS-PCR,rep-PCR对16S rRNA,gyrA,gyrB和rpoB基因进行表型和基因分型,鉴定出90种细菌。此外,筛选分离株的编码溶血性(HblC,HblD)和非溶血性肠毒素(NheA,NheB和NheC),细胞毒素K(CytK)和催吐毒素(EM1)的基因及其产生能力调查显示,短小芽孢杆菌属的种占优势(72.21%),即安全杆菌(B. safensis)(48),短小芽孢杆菌(B. pumilus)(7)和短小芽孢杆菌(B. pumilus sensu lato)(10)。芽孢杆菌的其他物种包括蜡状芽孢杆菌(11),巨大芽孢杆菌(4),枯草芽孢杆菌(4),解淀粉芽孢杆菌(2),暹罗芽孢杆菌(2),地衣芽孢杆菌(1)和Lysinibacillus louembei也被确定。在蜡状芽孢杆菌菌株中检​​测到溶血,非溶血和细胞因子毒素基因,它们也能够产生溶血素。在任何分离物中均未检测到催吐毒素基因。在任何非蜡状芽孢杆菌物种中均未检测到所筛选的毒素基因。

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