Phylogenetic characterization of several para- and meta-PCB dechlorinating Clostridium species: 16s rDNA sequence analyses

2000 ◽  
Vol 30 (3) ◽  
pp. 238-243 ◽  
Author(s):  
L.-H. Hou ◽  
S.K. Dutta
2014 ◽  
Vol 52 (12) ◽  
pp. 1056-1056
Author(s):  
Ok-Hwa Hwang ◽  
Sebastian Raveendar ◽  
Young-Ju Kim ◽  
Ji-Hun Kim ◽  
Tae-Hun Kim ◽  
...  

Sugar Tech ◽  
2012 ◽  
Vol 14 (4) ◽  
pp. 422-427 ◽  
Author(s):  
A. K. Verma ◽  
Shubhra Singh ◽  
Shalini Singh ◽  
Ashutosh Dubey

2014 ◽  
Vol 52 (11) ◽  
pp. 918-929 ◽  
Author(s):  
Ok-Hwa Hwang ◽  
Sebastian Raveendar ◽  
Young-Ju Kim ◽  
Ji-Hun Kim ◽  
Tae-Hun Kim ◽  
...  

2011 ◽  
Vol 63 (3) ◽  
pp. 697-704 ◽  
Author(s):  
A. Pavic ◽  
S. Stankovic ◽  
Zaklina Marjanovic

Available information on bacteria that influence the economically important white truffle (Tuber magnatum Pico) life cycle is scarce. From the ascocarp of white truffle we isolated a strain TMG 022C, capable for growth in nitrogendepleted conditions and assimilation of mannitol and trehalose. According to 16S rDNA sequence phylogeny, the strain was closely related to Sphingobium amiense. The strain had the ability to perform ammonification, reduce nitrate and solubilize Ca3(PO4)2, produce chitinase, lipase, phospholipase and ?-glucanase, but not cellulase, pectinase, protease and siderophores. The results suggest that Sphingobium sp. TMG 022C could have an influence on the Tuber magnatum life cycle through improved mycelium nutrition and ascocarp decomposition.


2000 ◽  
Vol 46 (3) ◽  
pp. 211-217 ◽  
Author(s):  
Razia Kutty ◽  
Hemant J Purohit ◽  
Purushottam Khanna

Pseudomonas sp. strain PH1 was isolated from soil contaminated with pharmaceutical and dye industry waste. The isolate PH1 could use m-aminophenol as a sole source of carbon, nitrogen, and energy to support the growth. PH1 could degrade up to 0.32 mM m-aminophenol in 120 h, when provided as nitrogen source at 0.4 mM concentration with citrate (0.5 mM) as a carbon source in the growth medium. The presence of ammonium chloride as an additional nitrogen source repressed the degradation of m-aminophenol by PH1. To identify strain PH1, the 16S rDNA sequence was amplified by PCR using conserved eubacterial primers. The FASTA program was used to analyze the 16S rDNA sequence and the resulting homology patterns suggested that PH1 is a Pseudomonas.Key words: m-aminophenol, resorcinol, DNA sequencing.


2004 ◽  
Vol 183 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Mette M. Svenning ◽  
Torsten Eriksson ◽  
Ulla Rasmussen

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

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