U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX23778922: GSM8117460: MG1655 dmhpR1; Escherichia coli str. K-12 substr. MG1655; RNA-Seq
1 ILLUMINA (NextSeq 1000) run: 3.9M spots, 231.8M bases, 81.4Mb downloads

External Id: GSM8117460_r1
Submitted by: AG K.Jung, LMU Munich
Study: Motility-activating mutations upstream of flhDC reduce acid shock survival of Escherichia coli
show Abstracthide Abstract
Many neutralophilic bacterial species try to evade acid stress with an escape strategy, which is reflected in the increased expression of genes coding for flagellar components. Extremely acid-tolerant bacteria, such as Escherichia coli, survive the strong acid stress, e.g. in the stomach of vertebrates. Recently, we were able to show that the induction of motility genes in E. coli is strictly dependent on the degree of acid stress, i.e. they are induced under mild acid stress but not under severe acid stress. However, it was not known to what extent fine-tuned expression of motility genes is related to fitness and the ability to survive periods of acid shock. In this study, we demonstrate that the expression of FlhDC, the master regulator of flagellation, is inversely correlated with acid shock survival of E. coli. We encountered this phenomenon when analyzing mutants from the Keio collection in which the expression of flhDC was altered by an IS element. These results suggest a fitness trade-off between acid tolerance and motility. Overall design: Comparison of genome-wide mRNA levels in E. coli MG1655 WT and dmhpR, as well as BW25113 and BW25113 mhpR::km (Keio collection) at pH 4.4 in LB medium.
Sample: MG1655 dmhpR1
SAMN40188372 • SRS20603655 • All experiments • All runs
Library:
Name: GSM8117460
Instrument: NextSeq 1000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: RNA was harvested using the miRNeasy Mini Kit (QIAGEN) in combination with the RNase-Free DNase Set (QIAGEN) following manufacturer's protocols. Ribosomal RNA depletion was performed using the NEBNext rRNA Depletion Kit for bacteria (NEB) following manufacturer's protocols. Integrity of RNA samples was evaluated by using the RNA 6000 Nano Kit (Agilent). cDNA libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB) following manufacturer's protocols. cDNA library quality was assessed by using a High Sensitivity DNA Kit (Agilent).
Runs: 1 run, 3.9M spots, 231.8M bases, 81.4Mb
Run# of Spots# of BasesSizePublished
SRR281481033,862,732231.8M81.4Mb2024-04-14

ID:
32072154

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...