DNA FINGERPRINTING IN STUDYING THE GENETIC DIVERSITY OF BETA VULGARIS L.

2018 ◽  
Vol 3 (58) ◽  
pp. 46-53
Author(s):  
Tatiana P. Fedulova ◽  
◽  
Dmitriy N. Fedorin ◽  
Mikhail A. Bogomolov ◽  
Galina G. Goleva ◽  
...  
2019 ◽  
Vol 3 (62) ◽  
pp. 46-53
Author(s):  
Tatiana P. Fedulova ◽  
◽  
Dmitriy N. Fedorin ◽  
Mikhail A. Bogomolov ◽  
Galina G. Goleva ◽  
...  

2014 ◽  
Vol 80 (14) ◽  
pp. 4398-4413 ◽  
Author(s):  
Sam Crauwels ◽  
Bo Zhu ◽  
Jan Steensels ◽  
Pieter Busschaert ◽  
Gorik De Samblanx ◽  
...  

ABSTRACTBrettanomycesyeasts, with the speciesBrettanomyces(Dekkera)bruxellensisbeing the most important one, are generally reported to be spoilage yeasts in the beer and wine industry due to the production of phenolic off flavors. However,B. bruxellensisis also known to be a beneficial contributor in certain fermentation processes, such as the production of certain specialty beers. Nevertheless, despite its economic importance,Brettanomycesyeasts remain poorly understood at the genetic and genomic levels. In this study, the genetic relationship between more than 50Brettanomycesstrains from all presently known species and from several sources was studied using a combination of DNA fingerprinting techniques. This revealed an intriguing correlation between theB. bruxellensisfingerprints and the respective isolation source. To further explore this relationship, we sequenced a (beneficial) beer isolate ofB. bruxellensis(VIB X9085; ST05.12/22) and compared its genome sequence with the genome sequences of two wine spoilage strains (AWRI 1499 and CBS 2499). ST05.12/22 was found to be substantially different from both wine strains, especially at the level of single nucleotide polymorphisms (SNPs). In addition, there were major differences in the genome structures between the strains investigated, including the presence of large duplications and deletions. Gene content analysis revealed the presence of 20 genes which were present in both wine strains but absent in the beer strain, including many genes involved in carbon and nitrogen metabolism, and vice versa, no genes that were missing in both AWRI 1499 and CBS 2499 were found in ST05.12/22. Together, this study provides tools to discriminateBrettanomycesstrains and provides a first glimpse at the genetic diversity and genome plasticity ofB. bruxellensis.


2002 ◽  
Vol 62 (3) ◽  
pp. 503-508 ◽  
Author(s):  
N. MORAES ◽  
J. S. MORGANTE ◽  
C. Y. MIYAKI

In this study we analyzed a population of Bradypus torquatus with individuals originally distributed in different localities of Bahia, and two populations of B. variegatus with individuals from Bahia and São Paulo States. Using the DNA fingerprinting method, we assessed the genetic variability within and between populations. Analysis of the DNA profiles revealed genetic similarity indices ranging from 0.34 ± 0.07 to 0.87 ± 0.04. Similar low levels of genetic variability were found only in isolated mammalian populations or among related individuals. This study presents the first analyses of genetic diversity in sloth populations.


2000 ◽  
Vol 37 (3) ◽  
pp. 79-87 ◽  
Author(s):  
H. M. Srivastava ◽  
H. N. Shahi ◽  
R. Kumar ◽  
S. Bhatnagar

2011 ◽  
Vol 334 (4) ◽  
pp. 282-289 ◽  
Author(s):  
M.A. Latif ◽  
Mohd Rafii Yusop ◽  
M. Motiur Rahman ◽  
M.R. Bashar Talukdar

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