Project description:Gordonia rubripertincta CWB2 and an erbium pre-adapted strain were cultivated with and without addition of erbium. Metabolites were extracted from the supernatant and detected by LC-MS/MS.
Project description:Gordonia rubripertincta CWB2 and an erbium pre-adapted strain were cultivated with and without addition of erbium. Metabolites were extracted from the supernatant and detected by LC-MS/MS in negative mode.
Project description:The siderophore production of Gordonia rubripertincta CWB2 was investigated with special regards to the effects of rare earth metals on siderophore production.
Project description:The siderophore production of Gordonia rubripertincta CWB2 was investigated with special regards to the effects of rare earth metals on siderophore production.
Project description:Investigation of gene expression level changes in Gordonia sp. KTR9 and Gordonia sp. KTR9 mutant GlnR upon exposure to high and low nitrogen conditions The Gordonia sp. KTR9 strain used in this study has been previously described by Thompson KT, Crocker FH, Fredrickson HL.2005. Mineralization of the cyclic nitramine explosive hexahydro-1,3,5-trinitro-1,3,5-triazine by Gordonia and Williamsia spp. Appl Environ Microbiol. 2005 Dec;71(12):8265-72.
Project description:Gordonia rubripertincta CWB2 was grown at 30 °C in minimal media with fructose (with and without Fe) and styrene as sole source of carbon, respectively. After 5 days of cultivation the culture was diluted 1/10 in fresh media and incubated for 24 h with the respective substrate in a set of four Erlenmeyer flasks. Prior harvesting the cells, 10 % of an ice-cold STOP-solution (10 % buffered phenol in ethanol) was added to the culture followed by centrifugation at 11,000 x g for 5 minutes at 4 °C. The supernatant was discarded and the pellet was stored until RNA isolation at -80 °C. To break up the cells, 150 µl of a 5 mg ml-1 lysozyme solution were added to the pellet, mixed and incubated at room temperature for 5 minutes. 450 µl of buffer RLT (Qiagen) and 50 mg of (0.1 mm) glass beads were added to resuspend and break the cells by repeated vortexing at 4 °C. The suspension was applied to QIAshredder column for homogenization and to remove particles from the sample. Extraction of total RNA Extraction was done by applying the RNeasy Mini Kit including on-column DNA digestion (Qiagen). Isolated RNA was stored at -80 °C and quality was controlled on the 2100 Bioanalyzer using the RNA 6000 Nano Kit (Agilent). RNA quality and quantity was again checked by an Agilent 2100 Bioanalyzer run (Agilent Technologies, Böblingen, Germany) and Trinean Xpose sytem (Gentbrugge, Belgium) prior and after rRNA depletion by Ribo-Zero rRNA Removal Kit (Bacteria) (Illumina, San Diego, CA, USA). TruSeq Stranded mRNA Library Prep Kit from (Illumina, (San Diego, CA, USA) was used to prepare the cDNA libraries to analyze the whole transcriptome. The resulting cDNAs were then sequenced paired end on an Illumina MiSeq and HiSeq 1500 system (San Diego, CA, USA) using 2 x 75 nt read length.
