2019 ◽  
pp. 1-10
Author(s):  
Femi, Ayoade ◽  
Scott Fayemi ◽  
Olumide Olukanni ◽  
Tosin Ogunbiyi ◽  
Paul Oluniyi

Aim: The present work was aimed at ensuring the accurate taxonomic identification of the fermentation organisms previously isolated from spontaneously fermented cassava for the purpose of safety assessment and quality assurance. Study Design: Purposive sampling method was used as all the five isolated organisms (from the previous study); 2 bacterial and 3 fungal organisms were characterized using molecular methods. Place and Duration of Study:  The genotypically characterized organisms are from a previous study carried out in May 2016 where lactic acid bacterial and fungal organisms were isolated from spontaneously fermented cassava.  Methodology: Genomic DNA was extracted from the lactic acid microorganisms and this was used as a template in a polymerase chain reaction (PCR) reaction. The 16s rRNA genes were amplified for the bacterial isolates while nuclear ribosomal internal transcribed spacer (ITS) genes were targeted for the fungal isolates. The amplicons were electrophoresed on 2% agarose gel prepared with Tris Borate Ethylenediamintetraacetate (TBE) buffers stained with ethidium bromide. The sizes of the corresponding amplicon captured on gel images were compared with that of the ladder to determine their sizes. Furthermore, sequences of the PCR products were analyzed and the chromatograms subjected to BLAST (Basic Local Alignment Search Tool) analyses to identify the lactic acid organisms. Results: The 3 fungal isolates were identified as Schizophyllum commune (MK 431022), Aspergillus oryzae (MK434151), Aspergillus sydowii (MK434152), while the bacterial isolates were identified as Bacillus spp (MK450345) and Bacillus spp (MK 449018). A high level of discrepancies was observed when the results of identification of the same isolates by biochemical methods in an earlier report were compared with the results from the present study using molecular methods.  Conclusion: The identification and characterization of the isolates and the discrepancies between the outcomes of the biochemical and molecular methods underscore the limitations of phenotypic (biochemical) methods in characterizing organisms that may eventually be used as starter organisms in food fermentation. The present result makes quality assurance and safety assessment of foods prepared using these organisms as starter organisms possible.


2019 ◽  
pp. 1-7
Author(s):  
Femi, Ayoade ◽  
Scott Fayemi ◽  
Tosin Ogunbiyi ◽  
Olumide Olukanni ◽  
Paul Oluniyi

Aim: In order to ensure the accurate taxonomic identification of the lactic acid organisms that were previously isolated from spontaneously fermented yam for safety assessment and quality assurance purposes, phenotypic and genetic identification data were compared. Study Design: Using the purposive sampling method, four microorganisms were characterized using molecular methods. Place and Duration of Study:  Isolates of lactic acid microorganisms (2 bacterial and 2 fungal organisms) from spontaneously fermented yam in a previous study carried out in May 2016 were genetically identified using molecular methods.  Methodology: Genomic DNA extracted from the test lactic acid microorganisms were used as templates in a PCR reaction, then, 16s rRNA and nuclear ribosomal internal transcribed spacer (ITS) genes were amplified for the bacterial and fungal isolates respectively. The polymerase chain reaction (PCR) products were electrophoresed on 2% agarose gel prepared with Tris Borate Ethylenediamintetraacetate (TBE) buffers stained with ethidium bromide. Subsequently, the ladder was used in order to determine the sizes of the corresponding amplicons captured on gel images in comparisons. Moreover, sequences of the PCR products were analyzed and the chromatograms subjected to BLAST (Basic Local Alignment Search Tool) analyses to identify the lactic acid organisms. Results: The 2 bacterial isolates were identified as Bacillus subtilis (MK448227) and Bacillus pumilus (MK446418), on the other hand, the fungal isolates were identified as Aspergillus flavus (MK433604) and Aspergillus niger (MK430926). Discrepancies were observed when phenotypic identification data in an earlier report were compared with the molecular data from the present study.  Conclusion: The present results underscore the limitations of phenotypic (biochemical) methods in characterizing organisms, particularly, organisms that may end up being used in food processing. Moreover, this is the first report of the novel organisms reported in the present study and makes further work into the development of starter organisms for the production of amala possible in the near future. In addition, proper identification helps in benchmarking the quality assurance and safety assessment of foods prepared using these organisms.


1999 ◽  
Vol 8 (1) ◽  
pp. 15-17
Author(s):  
Michael Groher ◽  
Caryn Easterling
Keyword(s):  

2008 ◽  
Vol 18 (2) ◽  
pp. 87-98 ◽  
Author(s):  
Vinciya Pandian ◽  
Thai Tran Nguyen ◽  
Marek Mirski ◽  
Nasir Islam Bhatti

Abstract The techniques of performing a tracheostomy has transformed over time. Percutaneous tracheostomy is gaining popularity over open tracheostomy given its advantages and as a result the number of bedside tracheostomies has increased necessitating the need for a Percutaneous Tracheostomy Program. The Percutaneous Tracheostomy Program at the Johns Hopkins Hospital is a comprehensive service that provides care to patients before, during, and after a tracheostomy with a multidisciplinary approach aimed at decreasing complications. Education is provided to patients, families, and health-care professionals who are involved in the management of a tracheostomy. Ongoing prospective data collection serves as a tool for Quality Assurance.


2019 ◽  
Vol 25 ◽  
pp. 173
Author(s):  
Magnus Löndahl ◽  
Mona Landin-Olsson ◽  
Stig Attval ◽  
Colleen Mdingi ◽  
Katherine S Tweden
Keyword(s):  

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