Deciphering the Probiotic Potential of Bacillus amyloliquefaciens COFCAU_P1 Isolated from the Intestine of Labeo rohita Through In Vitro and Genetic Assessment

Author(s):  
Md. Idrish Raja Khan ◽  
Dibyendu Kamilya ◽  
Tanmoy Gon Choudhury ◽  
Partha Sarathi Tripathy ◽  
Gaurav Rathore
2021 ◽  
Vol 9 (5) ◽  
pp. 1370-1383
Author(s):  
Xiaoyu Lei ◽  
Jian Wang ◽  
Jie Chen ◽  
Jing Gao ◽  
Jinzheng Zhang ◽  
...  

Combined with a series of antibacterial tests and the genetic assessment of the apoptotic pathway, an evaluation system has been rationalized to govern the fate of the different compositions of PU-based sealers.


2018 ◽  
Vol 6 (25) ◽  
Author(s):  
Thao D. Tran ◽  
Steven Huynh ◽  
Craig T. Parker ◽  
Robert Hnasko ◽  
Lisa Gorski ◽  
...  

ABSTRACT Here, we report the complete genome sequences of three Bacillus amyloliquefaciens strains isolated from alfalfa, almond drupes, and grapes that inhibited the growth of Listeria monocytogenes strain 2011L-2857 in vitro. We also report multiple gene clusters encoding secondary metabolites that may be responsible for the growth inhibition of L. monocytogenes.


Author(s):  
Kamni Rajput ◽  
Ramesh Chandra Dubey

In this paper, an investigation on lactic acid bacterial isolates from ethnic goat raw milk samples were examined for their probiotic potential and safety parameters. For this purpose, isolated bacterial cultures were screened based on certain parameters viz., sugar fermentation, tolerance to temperature, salt, low pH, bile salts, and phenol resistance. After that, these bacterial cultures were more estimated in vitro for auto-aggregation, cell surface hydrophobicity, response to simulated stomach duodenum channel, antibiotic resistance, and antimicrobial activity. Besides, probiotic traits show the absence of gelatinase and hemolytic activity supports its safety. The isolate G24 showed good viability at different pH, bile concentration, phenol resistance and response to simulated stomach duodenum passage but it did not show gelatinase and hemolytic activities. Isolate G24 was susceptible to amikacin, carbenicillin, kanamycin, ciprofloxacin, co-trimazine, nitrofurantoin, streptomycin, and tetracycline. Isolate G24 also exhibited antimicrobial action against five common pathogenic bacteria, such as Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Listeria monocytogens, and Salmonella typhimurium. It displayed the maximum auto-aggregation, cell surface hydrophobicity to different hydrocarbons. Following molecular characterization the isolate G24 was identified as Enterococcus hirae with 16S rRNA gene sequencing and phylogeny. E. hirae G24 bears the excellent properties of probiotics.


2017 ◽  
Vol 11 (1) ◽  
pp. 95-103
Author(s):  
Lamia Mermouri ◽  
Malika Dahmani ◽  
Aicha Bouhafsoun ◽  
Thierry Berges ◽  
Mourad Kacem ◽  
...  

Author(s):  
R.I. Tarakanov ◽  
◽  
P.A. Vasilyev ◽  
K.S. Troshin ◽  
F.-S. U. Dzhalilov

the article presents data on the effectiveness of biological preparations based on bacteria of the genus Bacillus against pathogens of soybean bacteriosis. The results show high activity of the biofungicide based on Bacillus amyloliquefaciens MBI600 both in vitro and in the vegetative experiment against bacterial blight.


2020 ◽  
Vol 110 (2) ◽  
pp. 317-326 ◽  
Author(s):  
Ayaz Farzand ◽  
Anam Moosa ◽  
Muhammad Zubair ◽  
Abdur Rashid Khan ◽  
Muhammad Ayaz ◽  
...  

Sclerotinia sclerotiorum is a devastating necrotrophic pathogen that infects multiple crops, and its control is an unremitting challenge. In this work, we attempted to gain insights into the pivotal role of lipopeptides (LPs) in the antifungal activity of Bacillus amyloliquefaciens EZ1509. In a comparative study involving five Bacillus strains, B. amyloliquefaciens EZ1509 harboring four LPs biosynthetic genes (viz. surfactin, iturin, fengycin, and bacilysin) exhibited promising antifungal activity against S. sclerotiorum in a dual-culture assay. Our data demonstrated a remarkable upsurge in LPs biosynthetic gene expression through quantitative reverse transcription PCR during in vitro interaction assay with S. sclerotiorum. Maximum upregulation in LPs biosynthetic genes was observed on the second and third days of in vitro interaction, with iturin and fengycin being the highly expressed genes. Subsequently, Matrix-assisted laser desorption/ionization-time of flight-mass spectrometry analysis confirmed the presence of LPs in the inhibition zone. Scanning electron microscope analysis showed disintegration, shrinkage, plasmolysis, and breakdown of fungal hyphae. During in planta evaluation, S. sclerotiorum previously challenged with EZ1509 showed significant suppression in pathogenicity on detached leaves of tobacco and rapeseed. The oxalic acid synthesis was also significantly reduced in S. sclerotiorum previously confronted with antagonistic bacterium. The expression of major virulence genes of S. sclerotiorum, including endopolygalacturonase-3, oxalic acid hydrolase, and endopolygalacturonase-6, was significantly downregulated during in vitro confrontation with EZ1509.


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