Isolation and Identification of Aroma-producing Yeast from Mackerel Fermentation Broth and Its Fermentation Characteristics

Author(s):  
Yu Wu ◽  
Xiao’e Chen ◽  
Xubo Fang ◽  
Lili Ji ◽  
Fang Tian ◽  
...  
2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Huawei Zhang ◽  
Chuanfen Ruan ◽  
Xuelian Bai ◽  
Miao Zhang ◽  
Shuangshuang Zhu ◽  
...  

Endophytic microbe has been proved to be one of rich sources of bioactive natural products with potential application for new drug and pesticide discovery. One cyclodepsipeptide, beauvericin, was firstly isolated from the fermentation broth ofFusarium oxysporum5-19 endophytic onEdgeworthia chrysanthaLinn. Its chemical structure was unambiguously identified by a combination of spectroscopic methods, such as HRESI-MS and1H and13C NMR. ESI-MS/MS was successfully used to elucidate the splitting decomposition route of the positive molecule ion of beauvericin. Antimicrobial results showed that this cyclodepsipeptide had inhibitory effect on three human pathogenic microbes,Candida albicans,Escherichia coli, andStaphylococcus aureus. In particular, beauvericin exhibited the strongest antimicrobial activity againstS. aureuswith MIC values of 3.91 μM, which had similar effect with that of the positive control amoxicillin.


Author(s):  
Li Pei-Xia ◽  
Jan Tian-Tian ◽  
Li Wei-Yi ◽  
He Dong-Hao ◽  
Huang Yi

Aims: To promote the rational exploration of the mushroom resources, this study evaluated the in vitro antioxidant activity of 16 kinds of mushrooms collected from the Sichuan province in China and completed the identification of the optimal active strains. Place and Duration of Study: School of Life Science and Engineering, Southwest University of Science and Technology, Mianyang, Sichuan province, China. April 2019 to May 2020 (13 Months). Methodology: 16 kinds of mushrooms were collected in the wild. These strains were isolated and cultivated. The extract’s antioxidant activities of fermentation broth and mycelium were assessed using the DPPH radical-scavenging method. The higher activity strains were also evaluated by Trolox equivalent antioxidant capacity (TEAC) and the Ferric reducing antioxidant power (FRAP) assay. Meanwhile, the contents of total flavonoids and total phenols were determined. Finally, The highly active strains were identified by internal transcribed spacer (ITS) Identification. Results: All extract of fermentation broth and mycelium from 16 kinds of mushrooms had scavenging effects on DPPH. Among them, strain No. 6 and No. 7 exhibited obvious antioxidant capacity, and the scavenging rates of their fermentation broths on DPPH were 89.47% and 84.27%, respectively. And the results of TEAC and FRAP were consistent with those of DPPH. Besides, these two kinds of mushrooms were all rich in phenolic and flavonoid compounds, and the content in the fermentation broth was significantly higher than that in the mycelium, indicating that phenolic and flavonoid substances may be the material basis of their antioxidant effect. The strain No. 6 and No. 7 were confirmed to be Bjerkandera and Nigrospora sp, respectively by 16S nrDNA sequence identification. Conclusion: The results showed that Bjerkandera and Nigrospora sp. possessed the highest antioxidant capacities with rich total phenolic and total flavonoids. They could be potential sources of natural antioxidants for further exploration and application.


2006 ◽  
Vol 73 (1) ◽  
pp. 168-178 ◽  
Author(s):  
Zengguo He ◽  
Duygu Kisla ◽  
Liwen Zhang ◽  
Chunhua Yuan ◽  
Kari B. Green-Church ◽  
...  

ABSTRACT A new bacterial strain, displaying potent antimicrobial properties against gram-negative and gram-positive pathogenic bacteria, was isolated from food. Based on its phenotypical and biochemical properties as well as its 16S rRNA gene sequence, the bacterium was identified as Paenibacillus polymyxa and it was designated as strain OSY-DF. The antimicrobials produced by this strain were isolated from the fermentation broth and subsequently analyzed by liquid chromatography-mass spectrometry. Two antimicrobials were found: a known antibiotic, polymyxin E1, which is active against gram-negative bacteria, and an unknown 2,983-Da compound showing activity against gram-positive bacteria. The latter was purified to homogeneity, and its antimicrobial potency and proteinaceous nature were confirmed. The antimicrobial peptide, designated paenibacillin, is active against a broad range of food-borne pathogenic and spoilage bacteria, including Bacillus spp., Clostridium sporogenes, Lactobacillus spp., Lactococcus lactis, Leuconostoc mesenteroides, Listeria spp., Pediococcus cerevisiae, Staphylococcus aureus, and Streptococcus agalactiae. Furthermore, it possesses the physico-chemical properties of an ideal antimicrobial agent in terms of water solubility, thermal resistance, and stability against acid/alkali (pH 2.0 to 9.0) treatment. Edman degradation, mass spectroscopy, and nuclear magnetic resonance were used to sequence native and chemically modified paenibacillin. While details of the tentative sequence need to be elucidated in future work, the peptide was unequivocally characterized as a novel lantibiotic, with a high degree of posttranslational modifications. The coproduction of polymyxin E1 and a lantibiotic is a finding that has not been reported earlier. The new strain and associated peptide are potentially useful in food and medical applications.


Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
YJ Lee ◽  
J Kim ◽  
J Lee ◽  
ES Cho ◽  
OS Bang

Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
CJ Ma ◽  
KY Lee ◽  
HK Yang ◽  
JS Yoon ◽  
YC Kim ◽  
...  

2012 ◽  
Vol 6 (2) ◽  
pp. 7-10
Author(s):  
Mohammad Murshed ◽  
Sabeena Shahnaz ◽  
Md. Abdul Malek

Isolation and identification of post operative hospital acquired infection was carried out from July 2008 to December 2008 in Holy Family Red Crescent Medical College Hospital (private hospital). The major pathogen of wound infection was E. coli. A total; of 120 samples were collected from the surrounding environment of post operative room like floor, bed sheets, instruments, dressing materials, catheter, nasogastric and endotracheal tube. E. coli (40%) was the predominant organism followed by S. aureus (24%). DNA fingerprinting analysis using pulsed field gel electreopheresis of XbaI restriction digested genomic DNA showed that clonal relatedness between the two clinical nd environmental isolates were 100%.DOI: http://dx.doi.org/10.3329/bjmm.v6i2.19369 Bangladesh J Med Microbiol 2012; 06(02): 7-10


2020 ◽  
Vol 26 (1-2) ◽  
pp. 73-78
Author(s):  
A Hossen ◽  
MH Rahman ◽  
MZ Ali ◽  
MA Yousuf ◽  
MZ Hassan ◽  
...  

Duck plague (DP) is the most important infectious disease of geese, ducks and free-ranging water birds. The present study was conducted to determine the prevalence of duck plague virus followed by isolation and identification. For these purposes, a total of 155 cloacal swabs samples were collected randomly from duck of different haor areas of Bangladesh including 45 (41 surveillance and 4 clinical) samples from Netrokona; 42 (40 surveillance and 2 clinical) samples from Kishoregonj; 30 samples from Brahmanbaria and 38 samples from Sunamganj. The samples were processed and pooled (1:5 ratio) for initial screening of target polymerase gene of duck plague virus by polymerase chain reaction (PCR) method. All the samples of a positive pool were then tested individually for identifying the individual positive samples. The result showed that out of 155 samples, 41 (26.45%) were found positive in which 17 were from Netrokona, where 15 (36.58%) were from surveillance samples and 2 (50%) were from clinical sample; 16 were from Kishoregonj, where 14 (35%) were from surveillance samples and 2 (100%) were from clinical sample; 2 (6.6%) were from Brahmanbaria and 5 (13.15%) were from Sunamganj. These positive samples were inoculated into 9-10 days embryonated duck eggs (EDE) through chorioallantoic membrane (CAM) route for the isolation of virus. The EDE died earlier was also chilled, and in a similar way, the CAMs were collected and again performed PCR for id entification of virus. Out of 41 PCR positive samples, 26 samples were isolated and reconfirmed by PCR. Subsequently, DPV was isolated in primary duck embryo fibroblasts cell culture and confirmed by observing cytopathic effect (CPE). Bang. J. Livs. Res. Vol. 26 (1&2), 2019: P. 73-78


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