scholarly journals Antimicrobial Spectrum, Growth/Killing Kinetics, Conventional/Molecular Assay of Characterizing Non-Leguminous Endophytic Bacteria and Fungi from Helianthus annuus, Carica papaya and Lycoperesicum solanum

2021 ◽  
Vol 2 (10) ◽  
pp. 1018-1034
Author(s):  
Osuntokun OT ◽  
Azuh VO ◽  
Adejoro BF ◽  
Akele EO

The aim of this study is to comparative study between conventional and molecular assay of isolation, identification and characterization of non-leguminous endophytic bacteria and fungi in the leguminous root samples. The plant root samples, Helianthus annuus, Carica papaya and Lycoperesicum solanum (Sunflower root and stem, pawpaw root and stem, and tomato root and stem from Adekunle Ajasin University School farm, Akungba Akoko, Ondo state, Nigeria. The isolation of endophytic bacteria were performed using the conventional method of isolation (biochemical test) and characterization were done using both the conventional and molecular method of bacteria characterization. The antibiotic susceptibility test (Antibiogram) was observed using disc diffusion. The four bacteria identified were Bacillus cereus, Enterobacter sp. Actnomycoses sp. and Aeromonas sp. for conventional method and Fusarium solani, Fusarium vortecelium and Bacillus thuringiensis for molecular method as confirmatory point of view. In this study, all isolated organisms tends to be Gram positive using the gram staining technique. Antibiogram shows the zones of inhibition with diameter ranging from 0-20 mm, Enterobacter sp. were more sensitive to the various antibiotics used. Ultraviolet spectrophotometer was also used to determine the growth dynamic as well as the death rate of the isolates, the addition of antibiotics (ciprofloxacin) to the isolates at the 24th hour speed up the death rate of the isolates from non-leguminous endophytic bacteria. After the preliminary identification of the bacteria isolates and the confirmatory identification of both bacteria and fungi isolates of the non-leguminous endophytic microorganism, it was noted that the preliminary identification was only able to achieve the genus level of taxonomic characterization, While the molecular method confirm the molecular sub level identification of isolates depletes the absolute taxonomic identification and characterization to the sub-species level. The results of this study validates the use of molecular sequencing for the assay identification and characterization of non-leguminous endophytic bacteria and fungi as the easy and best mode of identification of both bacteria and fungi isolates as a veritable tools for research purposes.

2016 ◽  
Vol 124 ◽  
pp. 29-37 ◽  
Author(s):  
Anna-Katharina Aschenbrenner ◽  
Moonhyuk Kwon ◽  
Jürgen Conrad ◽  
Dae-Kyun Ro ◽  
Otmar Spring

2019 ◽  
Vol 155 (4) ◽  
pp. 1077-1091 ◽  
Author(s):  
Wael Alsultan ◽  
Ganesan Vadamalai ◽  
Ahmad Khairulmazmi ◽  
Halimi Mohd Saud ◽  
Abdullah M. Al-Sadi ◽  
...  

AMB Express ◽  
2014 ◽  
Vol 4 (1) ◽  
Author(s):  
Vivian Jaskiw Szilagyi-Zecchin ◽  
Angela Cristina Ikeda ◽  
Mariangela Hungria ◽  
Douglas Adamoski ◽  
Vanessa Kava-Cordeiro ◽  
...  

IUBMB Life ◽  
2020 ◽  
Vol 72 (5) ◽  
pp. 991-1000
Author(s):  
Elaheh Zadeh Hosseingholi ◽  
Neda Neghabi ◽  
Ghader Molavi ◽  
Seyed Mohammad Gheibi Hayat ◽  
Hamed Shahriarpour

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Rea Valaperta ◽  
Valeria Sansone ◽  
Fortunata Lombardi ◽  
Chiara Verdelli ◽  
Alessio Colombo ◽  
...  

The expansion of the specific trinucleotide sequence, [CTG], is the molecular pathological mechanism responsible for the clinical manifestations of DM1. Many studies have described different molecular genetic techniques to detect DM1, but as yet there is no data on the analytical performances of techniques used so far in this disease. We therefore developed and validated a molecular method, “Myotonic Dystrophy SB kit,” to better characterize our DM1 population. 113 patients were examined: 20 DM1-positive, 11 DM1/DM2-negative, and13 DM1-negative/DM2-positive, who had a previous molecular diagnosis, while 69 were new cases. This assay correctly identified 113/113 patients, and all were confirmed by different homemade assays. Comparative analysis revealed that the sensitivity and the specificity of the new kit were very high (>99%). Same results were obtained using several extraction procedures and different concentrations of DNA. The distribution of pathologic alleles showed a prevalence of the “classical” form, while of the 96 nonexpanded alleles 19 different allelic types were observed. Cardiac and neuromuscular parameters were used to clinically characterize our patients and support the new genetic analysis. Our findings suggest that this assay appears to be a very robust and reliable molecular test, showing high reproducibility and giving an unambiguous interpretation of results.


1986 ◽  
Vol 14 (6) ◽  
pp. 1226-1227 ◽  
Author(s):  
BALDEV S. BAINES ◽  
KEITH BROCKLEHURST ◽  
RAYMOND McKEE ◽  
MAIREAD O'DRISCOLL ◽  
ERDJAN SALIH ◽  
...  

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