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Items: 1 to 20 of 17230

1.

Desiccation induces varied responses within a soil bacterial genus

(Submitter supplied) Nine Curtobacterium strains (three from three clades) were subjected to a lab desiccation experiment with no access to moisture or nutrients to compare between clades. RNA was extracted at days 0, 1, and 32 and sequenced
Organism:
Curtobacterium
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33356
81 Samples
Download data: CSV, SF
Series
Accession:
GSE230266
ID:
200230266
2.

The Fur-like regulatory protein MAP3773c modulates key metabolic pathways in Mycobacterium avium subsp. paratuberculosis under in-vitro iron starvation

(Submitter supplied) Mycobacterium avium subsp. paratuberculosis (MAP) carries MAP3773c, a putative metal regulator, on its genome which is absent in other mycobacteria. Homologues of this gene in enterobacteria have roles in global iron regulation and homeostasis. The role of MAP3773c in regulating intracellular iron in MAP is poorly understood. Functional analysis of DEGs in ΔMAP3773c revealed that pantothenate (Pan) biosynthesis, polysaccharide biosynthesis, sugar metabolism and N-acetyltransferase enhanced intracellular survival genes were downregulated at 30 minutes post-iron starvation whereas ATP-binding cassette (ABC) type metal transporters, putative siderophore biosynthesis, arginine and proline metabolism, PPE, PE family and mammalian cell entry (MCE) genes were upregulated at that same time point. more...
Organism:
Mycobacterium avium subsp. paratuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33823
20 Samples
Download data: TXT
Series
Accession:
GSE244734
ID:
200244734
3.

Co-existence of CBB cycle and rTCA carbon fixation pathway in thermophilic Actinomycetota Carbonactinospora thermoautotrophica StC and correlation with the CO2-concentrating microcompartment

(Submitter supplied) Seven carbon autotrophic fixation pathways were described so far. However, it is not common to find the co-existence of more than one cycle in a single cell. Here, we describe a thermophilic bacterium Carbonactinospora thermoautotrophica StC with a unique and versatile carbon metabolism. StC was isolated from a consortium found in a burning organic pile that exhibits an optimal growth temperature between 55° and 65° C. more...
Organism:
Carbonactinospora thermoautotrophica
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34357
14 Samples
Download data: FA, TXT
Series
Accession:
GSE263135
ID:
200263135
4.

A cell-free pipeline for recreating methylation patterns radically enhances DNA transformation in bacteria

(Submitter supplied) The bacterial world offers diverse strains for understanding medical and environmental processes and for engineering synthetic-biology chasses. However, genetically manipulating these strains has faced a long-standing bottleneck: how to efficiently transform DNA. Here we report IMPRINT, a generalized, rapid and scalable approach to overcome DNA restriction, a prominent barrier to transformation. IMPRINT utilizes cell-free systems to express DNA methyltransferases from the bacterial host’s restriction-modification systems. more...
Organism:
Escherichia coli; Bifidobacterium breve
Type:
Other
Platforms:
GPL25368 GPL33564
7 Samples
Download data: TSV
Series
Accession:
GSE240651
ID:
200240651
5.

Maize root bacteria degrade host-specialized metabolites through the lactonase BxdA

(Submitter supplied) Root exudates contain specialised metabolites that affect the plant’s root microbiome. How host-specific microbes cope with these bioactive compounds, and how this ability shapes root microbiomes, remains largely unknown. We investigated how maize root bacteria metabolise benzoxazinoids, the main specialised metabolites of maize. Diverse and abundant bacteria metabolised the major compound in the maize rhizosphere MBOA and formed AMPO. more...
Organism:
Microbacterium sp. LMB2-1.2
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34376
10 Samples
Download data: TXT
Series
Accession:
GSE263275
ID:
200263275
6.

Allosteric regulation by c-di-AMP modulates global signal integration in Actinobacteria

(Submitter supplied) C-di-AMP is primarily associated with the regulation of carbon utilization as well as other central traits, central metabolism, and bacterial stringent response to environmental changes. Elevated c-di-AMP levels result in aberrant physiology for most c-di-AMP synthesizing organisms, drawing particular attention to the importance of the c-di-AMP homeostasis and the molecular mechanisms pertaining to nucleotide metabolism and signal transduction. more...
Organism:
Saccharopolyspora erythraea
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33125
4 Samples
Download data: TDF
Series
Accession:
GSE229938
ID:
200229938
7.

The catabolism of ethylene glycol by Rhodococcus jostii RHA1 and its dependence on mycofactocin

(Submitter supplied) Ethylene glycol (EG) is a widely used industrial chemical with manifold applications and is also generated in the degradation of plastics such as PET. Rhodococcus jostii RHA1 (RHA1), a potential biocatalytic chassis, grows on EG. Transcriptomic analyses revealed four clusters of genes potentially involved in EG catabolism: the mad locus, predicted to encode mycofactocin-dependent alcohol degradation, including the catabolism of EG to glycolate; two GCL clusters, predicted to encode glycolate and glyoxylate catabolism; and the mft genes, predicted to specify mycofactocin biosynthesis. more...
Organism:
Rhodococcus jostii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34291
12 Samples
Download data: TSV
Series
Accession:
GSE261336
ID:
200261336
8.

Development of gene expression signatures in whole spectrum of leprosy

(Submitter supplied) To further development of our gene expression approach in different groups of leprosy, we have employed whole genome microarray expression profiling as a discovery platform to identify genes with the potential to distinguish leprosy reactions and relapse cases from healthy controls. Human biopsy and skin slit were collected from reaction cases, PB cases, MB cases, relapse cases and healthy contacts. more...
Organism:
Mycobacterium leprae
Type:
Expression profiling by array
Platform:
GPL33105
45 Samples
Download data: TXT
Series
Accession:
GSE224736
ID:
200224736
9.

The natural product co-evolved pyrroloquinoline quinone operon enhances their production when heterologously expressed in a variety of Streptomycetes

(Submitter supplied) Streptomyces has the largest repertoire of natural product biosynthetic gene clusters (BGCs), yet developing a universal engineering strategy for each Streptomyces species is challenging. Given that some Streptomyces species have larger BGC repertoires than others, we hypothesized that a set of genes co-evolved with BGCs to support biosynthetic proficiency must exist in those strains, and that their identification may provide universal strategies to improve the productivity of other strains. more...
Organism:
Streptomyces griseus; Streptomyces rapamycinicus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL27559 GPL34215
12 Samples
Download data: CSV
Series
Accession:
GSE256209
ID:
200256209
10.

MftG is crucial for alcohol metabolism of mycobacteria by linking mycofactocin oxidation to respiration

(Submitter supplied) Mycofactocin is a redox cofactor essential for the alcohol metabolism of Mycobacteria. While the biosynthesis of mycofactocin is well established, the mftG gene, which encodes an oxidoreductase of the glucose-methanol-choline superfamily remained functionally uncharacterized. Here, we show that MftG enzymes strictly require mft biosynthetic genes, and are found in 75% of organisms harboring these genes. more...
Organism:
Mycolicibacterium smegmatis MC2 155
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28006
12 Samples
Download data: XLSX
Series
Accession:
GSE250373
ID:
200250373
11.

Translatome analysis by Ribosome profiling of Streptomyces coelicolor A3(2) cold-shock response

(Submitter supplied) Ribosome profiling analysis of wild type prototrophic Streptomyces coelicolor A3(2) MT1110 strain to examine global translational vs transcriptional profile change when exposed to cold shock from 30°C to 10°C in minimal liquid medium.
Organism:
Streptomyces coelicolor
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28977
30 Samples
Download data: CSV, TSV
Series
Accession:
GSE230542
ID:
200230542
12.

Translatome analysis by Polysome profiling of Streptomyces coelicolor A3(2) cold-shock response

(Submitter supplied) Polysome profiling analysis of wild type prototrophic Streptomyces coelicolor A3(2) MT1110 strain to examine global translational vs transcriptional profile change when exposed to cold shock from 30°C to 10°C in minimal liquid medium.
Organism:
Streptomyces coelicolor A3(2)
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26763
27 Samples
Download data: CSV, TSV
Series
Accession:
GSE229820
ID:
200229820
13.

Transcriptome analysis of cold-shock response in rich liquid (YEME), supplemented minimal solid (SMM) and supplemented minimal liquid (SMMS) media

(Submitter supplied) RNA-seq analysis of wild type prototrophic Streptomyces coelicolor A3(2) MT1110 strain to examine global transcriptional profile change when exposed to cold shock from 30°C to 10°C in rich liquid medium, minimal solid medium and in minimal liquid medium
Organism:
Streptomyces coelicolor A3(2)
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26763
36 Samples
Download data: CSV, TSV
Series
Accession:
GSE225850
ID:
200225850
14.

Establishing the conditions required to initiate a cold-shock response in Streptomyces coelicolor

(Submitter supplied) RNA-seq analysis of wild type Streptomyces coelicolor A3(2) MT1110 to examine global transcriptional profile change when exposed to cold shock from 30°C to 10°C in rich liquid medium and from 30°C to 4°C on minimal solid medium.
Organism:
Streptomyces coelicolor A3(2)
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26763
24 Samples
Download data: TSV
Series
Accession:
GSE220990
ID:
200220990
15.

Transcriptional profiling of M. intracellulare under acidic and oxidative stress conditions

(Submitter supplied) Mycobacterium avium complex (MAC), including Mycobacterium avium and Mycobacterium intracellulare (MI), accounts for a significant portion of nontuberculous mycobacterial lung disease affecting immunocompromised and lung structural disease patients. Adapting pathogens to a host-induced hostile environment is critical to establishing infection and persistence within the host. However, the cellular and molecular mechanisms of stress response for MAC still need to be elucidated. more...
Organism:
Mycobacterium intracellulare
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33797
9 Samples
Download data: TXT
Series
Accession:
GSE244264
ID:
200244264
16.

M.tb adaptation to human alveolar lining fluid (ALF)

(Submitter supplied) Superbugs such as drug-resistant Mycobacterium tuberculosis (DR-M.tb) poses a serious global health threat. Upon infection, M.tb reaches the alveolar space and comes in close contact with soluble components of the human alveolar lining fluid (ALF) for an uncertain period of time prior to and following its encounter with alveolar compartment cells. Homeostatic ALF hydrolases, which main function is maintaining lung health, modify the M.tb cell envelope, driving M.tb-host cell interactions. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22688
32 Samples
Download data: TXT
Series
Accession:
GSE228998
ID:
200228998
17.

Transcriptional regulator DhyR positively modulates biosynthesis of daptomycin in Streptomyces rosesporus

(Submitter supplied) The production of daptomycin (DAP) is precisely regulated by a complex regulatory network in Streptomyces roseosporus (S. roseosporus). Although the most biosynthetic pathway of DAP has been elucidated, the regulatory mechanism of its biosynthesis at transcriptional level is not fully understood. In the present study, a transcriptional regulator DhyR has been identified based on our previous quantification proteomics identification in S. more...
Organism:
Streptomyces filamentosus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34032
2 Samples
Download data: TXT
Series
Accession:
GSE251775
ID:
200251775
18.

Dual-active oxadiazoles targeting the Mycobacterium tuberculosis ESX-1 secretion system and boosting ethionamide activity 

(Submitter supplied) To find potential regulatory targets of the anti-virulence compound S3 in Mycobacterium tubercuolsis.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27507
4 Samples
Download data: TXT
Series
Accession:
GSE226474
ID:
200226474
19.

Gene expression in glucose-grown L-pipecolic acid production strains C.glutamicum LPA-1A and LPA-5 compared to the non-L-pipecolic acid-producing strain C. glutamicum LPA-0

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Corynebacterium glutamicum
Type:
Expression profiling by array
Platform:
GPL32785
12 Samples
Download data: TXT
Series
Accession:
GSE216736
ID:
200216736
20.

Gene expression in glucose-grown L-pipecolic acid production strains C.glutamicum LPA-1A and LPA-5 compared to the non-L-pipecolic acid-producing strain C. glutamicum LPA-0 [2]

(Submitter supplied) mRNA was sampled during exponential growth (OD660 = 4) strains: LPA-0 (L-lysine hyperproducing strain C. glutamicum LYS-12 (Becker et al. 2011) + pClik5a_MCS), C. glutamicum LPA-5 (C. glutamicum LPA-0 + pClik5a_peftu_lat_proC)
Organism:
Corynebacterium glutamicum
Type:
Expression profiling by array
Platform:
GPL32785
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE216735
ID:
200216735
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