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SRX8485153: GSM4594096: B. subtilis PY79 + E. coli MW1255; Escherichia coli; Bacillus subtilis; OTHER
1 ILLUMINA (NextSeq 550) run: 108.4M spots, 17.3G bases, 7.8Gb downloads

Submitted by: NCBI (GEO)
Study: Microbial single-cell RNA sequencing by split-pool barcoding
show Abstracthide Abstract
We introduce microSPLiT, a low cost and high-throughput single-cell RNA-sequencing method for gram-negative and gram-positive bacteria. We applied microSPLiT to >25,000 Bacillus subtilis cells sampled at different growth stages, creating a detailed atlas of changes in metabolism and lifestyle. We not only retrieve detailed gene expression profiles associated with known, but rare, states such as competence and PBSX prophage induction, but also identify novel and unexpected gene expression states including a heterogeneous activation of a niche metabolic pathway (myo-inositol catabolism) in a subpopulation of cells. Overall design: Single-cell RNA-seq (microSPLiT) was used to sample ten optical density (OD) points along the growth curve of the laboratory strain PY79 in LB medium ranging from OD0.5 to 6.0, with one replicate of 4 OD points. For validation of the method, we grew E. coli MW1255 and B. subtilis PY79 cells to OD600=0.5 and subjected half of each culture to a brief 47°C heat-shock. We performed a microSPLiT experiment on both samples, using the first barcode as a sample identifier.
Sample: B. subtilis PY79 + E. coli MW1255
SAMN15154358 • SRS6785174 • All experiments • All runs
Library:
Instrument: NextSeq 550
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: PAIRED
Construction protocol: Cells were fixed in cold formaldehyde overnight, permeabilized with Tween-20 and Lysozyme, then subjected to in-situ polyadenylation, reverse transcription and barcode ligation reactions. After barcoding, cells were lysed with proteinase K and barcoded cDNA was extracted on streptavidin beads Barcoded cDNA bound to streptavidin C1 beads had a 3' adapter appended through template switching, followed by qPCR amplification and fragmentation with WGS Fragmentation Mix (Enzymatics). Adapters for Illumina sequencing were then appended by the final round of PCR. SPLiT-seq, first barcode records sample identity
Experiment attributes:
GEO Accession: GSM4594096
Links:
Runs: 1 run, 108.4M spots, 17.3G bases, 7.8Gb
Run# of Spots# of BasesSizePublished
SRR11940662108,412,79917.3G7.8Gb2020-07-04

ID:
11027559

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