Total first strand cDNA was produced with random hexamer primers (Random Primer 6 5′d(N6)3′, Biolabs) using either PowerScript Reverse Transcriptase (Clonetech) or PrimeScript Reverse Transcriptase (Takara). The quality of each template cDNA was checked using the Bioanalyzer 2100 (Agilent). qPCR was performed using specific primers (75-100 nM each) according to the recommended protocol for each SYBR Green mix used (SYBR Green MasterMix 2X from ABgene or MESA GREEN MasterMix from Eurogentec). Reactions were run on an ABI PRISM 7900 HT instrument (Applied Biosystems) or a Mastercycler Realplex 2 S instrument
(Eppendorf) using https://www.selleckchem.com/screening/fda-approved-drug-library.html 40 cycles of denaturation at 95°C for 15 s and extension at 60°C for 1 min. The cycles were preceded MG-132 manufacturer by DNA polymerase activation at 95°C and followed by a denaturation cycle to check the specificity of the PCR products. Mean Ct obtained for studied genes were between 16 and 28.5, with the exception of comC and dprA in WT strain at 31 and 32.9 respectively (in the same time ‘No Template Controls’ gave no signal after 34 cycles). Primers were designed with Primer Express 2 (Applied Biosystems) or Primer 3 http://frodo.wi.mit.edu/primer3 and validated by determining slopes of standard curves for PCR efficiencies between 90% and 100%. In this context, we used the 2-ΔΔCt method to express results as
fold change in the expression of each gene of interest relative to a calibrator sample and a reference gene used as an internal control for normalization of the results [55]. The stability of transcription Interleukin-2 receptor of the chosen reference gene ldh was checked by standard curves
performed for all environmental conditions used in this study. Unless otherwise indicated, quantitation experiments were performed with three independent samples, each well being duplicated two or three times. Values are expressed as mean ± standard deviation. Viability and UV assays Viable bacteria were counted by plating serial dilutions on MRS agar and incubating at 30°C for one to four days. For mixed cultures, classical enumeration on MRS supplemented with Xgal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside, 0.04 g.l-1) distinguished sigH(hy)* (white) from sigH(wt)* (blue) as well as sigH(nul) (white) from 23 K lacLM + (blue). For other tests, sampling for stationary phase survival in MCD was done after 6-8 hour culturing which corresponds to growth arrest, then once or twice a day. In these cases, comparative enumeration was performed by depositing drops (5 μl) of serial decimal dilutions for each strain on an agar plate. UV resistance was examined by exposing bacteria freshly plated on MRS medium to 254 nm UV-light (VL-15 C, Apelex) with fluences of 40 to 120 J/m2 (by step of 20) measured by the radiometer VLX-3 W equipped with a 254 nm sensor (Vilber Lourmat, France).
Related posts:
- In the DASL assay, total RNA was first converted into cDNA in a r
- RNA
isolation Total RNA was extracted from mononuclear ce - Similarly on the short RNA libraries, the degradome cDNA library
- The particular primers employed within this re action were as fol
- Total length cDNA encoding human WIPI was amplified by PCR from t