Sphaerocavum: a coccoid morphogenus identical to Microcystis in terms of 16S rDNA and ITS sequence phylogenies

Hydrobiologia ◽  
2017 ◽  
Vol 811 (1) ◽  
pp. 35-48 ◽  
Author(s):  
Janaina Rigonato ◽  
Célia L. Sant’Anna ◽  
Alessandra Giani ◽  
Mª Teresa P. Azevedo ◽  
Watson A. Gama ◽  
...  
Keyword(s):  
16S Rdna ◽  
Author(s):  
Dong Ju Lee ◽  
Il-Chul Kim

This is the first report of a freshwater crab (Naju crab) collected from the Korean peninsula. It was named after Naju city. The Naju crab was identified based on evidence of 2 mitochondrial DNA of 16S rDNA and cytochrome oxidase subunit1 (COI), supporting that the Naju crab belongs to the genus Geothelphusa. The variances of the nucleotide sequence of 16S rDNA are from 2.01% to 6.02% between the Naju crab and four G. dehaani isolates (AB290630, AB551391, AB187570, and AB535460, respectively). The variances of the nucleotide sequence of CO1 are from 2.58% to 7.96% between the Naju crab and four G. dehaani isolates (AB551393, AB187570, AB290648, and AB535491, respectively). The nuclear internal transcribed spacer (ITS) sequence (1515bp) of the Naju crab showed that its 5.8S nucleotide sequence was highly conserved to that of Sesarma spp, terrestrial crab endemic to the American continent. However, the nucleotide sequences of the ITS1 and the ITS2 are not found to be conserved in any species in the world.


2021 ◽  
Vol 79 (1) ◽  
Author(s):  
Karuppusamy Shanmugasundaram ◽  
Harisankar Singha ◽  
Sheetal Saini ◽  
Bhupendra N. Tripathi

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
YH Kim ◽  
JA Ryuk ◽  
BS Ko ◽  
JW Lee ◽  
SE Oh ◽  
...  

2012 ◽  
Vol 3 (3) ◽  
pp. 302-304
Author(s):  
G. D.Sharma G. D.Sharma ◽  
◽  
* Dhritiman Chanda ◽  
D.K. Jha D.K. Jha

2018 ◽  
Vol 4 (3) ◽  
pp. 80-85
Author(s):  
YU.А. LEONTIEVA ◽  
◽  
A.G. NALIAN ◽  
G.A. DAMOFF ◽  
A.V. MARTYNOVA-VAN KLEY ◽  
...  

2012 ◽  
pp. 15-19
Author(s):  
Thi Chau Anh Nguyen ◽  
Hoang Bach Nguyen ◽  
Hai Duong Huynh ◽  
Nu Xuan Thanh Le ◽  
Xuan Cuong Le ◽  
...  

Background: The Nested IS6110 PCR is used for detecting tuberculosis, however IS6110 sequence is not present in the genome of all strains of M.tuberculosis, the result may be false negative. The gene coding 16S ribosome always contains a short sequence specific to M. tuberculosis complex. Objects: Performance of the 16S Real-time PCR to detect M. tuberculosis and combining to the nested IS6110 PCR to determine the rate of Mtb strains without IS6110 from clinical samples. Materials and method: Performance of 16S rDNA PCR by commercial kit of Viet A Inc. for all 480 samples, the samples which were positive with the 16S rDNA PCR were retested in IS6110 PCR assay by in-house kit. Results: The Realtime 16S rDNA PCR detected 258 cases (53.8%) of tuberculosis. There were 3 (1.2 %) M. tuberculosis strains which do not harbor IS6110 sequence in genome. Conclusion: The IS6110 nested PCR can be applied more widely than the 16S rDNA realtime PCR. In case of using IS6110 PCR assay, results may show a low proportion of false negative. Combining 16S rDNA PCR with the IS6110 based PCR allowed detection of deletion of IS6110 sequence in M. tuberculosis isolates.


2008 ◽  
Vol 16 (6) ◽  
pp. 586 ◽  
Author(s):  
Zhang Jianping ◽  
Dong Naiyuan ◽  
Yu Haobin ◽  
Zhou Yongjun ◽  
Lu Yongliang ◽  
...  

1998 ◽  
Vol 37 (4-5) ◽  
pp. 303-306 ◽  
Author(s):  
R. Howarth ◽  
I. M. Head ◽  
R. F. Unz

Nearly complete 16S ribosomal RNA (rRNA) sequences were determined for fully characterised axenic strains of Thiothrix, Eikelboom type O21N, and Eikelboom type 1701 originally isolated from bulking activated sludges. Thiothrix strains formed a monophyletic group (100% bootstrap support) with previously described Thiothrix nivea strain JP2 and Thiothrix ramosa. Eikelboom type O21N strain AP3 revealed a sufficiently strong relationship to the Thiothrix group to suggest a common ancestry for the two organism although it was not possible to designate type 021N as a species of Thiothrix. Eikelboom type 1701 contained within its sequence the target sequence of an oligonucleotide probe for the detection of Sphaerotilus natans.


2019 ◽  
Vol 17 ◽  
Author(s):  
Farzane Kargar ◽  
Mojtaba Mortazavi ◽  
Mahmood Maleki ◽  
Masoud Torkzadeh Mahani ◽  
Younes Ghasemi ◽  
...  

Aims: The purpose of this study was to screen the bacteria producing cellulase enzymes and their bioinformatics studies. Background: Cellulose is a long-chain polymer of glucose that hydrolyzes by cellulases to glucose molecules. In order to design the new biotechnological applications, some strategies have been used as increasing the efficiency of enzyme production, generating cost-effective enzymes, producing stable enzymes and identification of new strains. Objective: On the other hand, some bacteria special features have made them suitable candidates for the identification of the new source of enzymes. In this regard, some native strains of bacteria were screened. Method: These bacteria were grown on a culture containing the liquid M9 media containing CMC to ensure the synthesis of cellulase. The formation of a clear area in the culture medium indicated decomposition of cellulose. In the following, the DNA of these bacteria were extracted and their 16S rDNA genes were amplified. Result: The results show that nine samples were able to synthesize cellulase. In following, these strains were identified using 16S rDNA. The results show that these screened bacteria belonged to the Bacillus sp., Alcaligenes sp., Alcaligenes sp., and Enterobacter sp.conclusionThe enzyme activity analysis shows that the Bacillus toyonensis, Bacillus sp. strain XA15-411 Bacillus cereus have produced the maximum yield of cellulases. However, these amounts of enzyme production in these samples are not proportional to their growth rate. As the bacterial growth chart within 4 consecutive days shows that the Alcaligenes sp. Bacillus cereus, Bacillus toyonensis, Bacillus sp. strain XA15-411 have a maximum growth rate. The study of the phylogenetic tree also shows that Bacillus species are more abundant in the production of cellulase enzyme. These bioinformatics analyses show that the Bacillus species have different evolutionary relationships and evolved in different evolutionary time. Other: However, for maximum cellulase production by this bacteria, some information as optimum temperature, optimum pH, carbon and nitrogen sources are needed for the ideal formulation of media composition. The cellulase production is closely controlled in microorganisms and the cellulase yields appear to depend on a variety of factors. However, the further studies are needed for cloning, purification and application of these new microbial cellulases in the different commercial fields as in food, detergent, and pharmaceutical, paper, textile industries and also various chemical industries. However, these novel enzymes can be further engineered through rational design or using random mutagenesis techniques.


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