Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Fictibacillus solisalsi strain:cgmcc 1.6854

ABSTRACT: Bacillus solisalsi CGMCC 1.6854 genome sequencing

PROVIDER: PRJNA303880 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Similar Datasets

phbC plays an important role in curdlan biosynthesis of Agrobacterium sp. CGMCC 11546

Project description:Purpose： The goal of this study is compare the effect of phbC gene in curdlan synthesis in Agrobacterium sp. CGMCC 11546. methods: The transcriptional and metabolomics analysis the function of phbC in Agrobacterium sp. CGMCC 11546. Results:The transcriptional and metabolomics showed that the decrease of curdlan production in the ΔphbC mutants may be caused by the insufficient supply of energy ATP conclusion:phbC play an important role in curdlan synthesis in Agrobacterium sp. CGMCC 11546

2022-06-30 | GSE153504 | GEO

Salibacterium qingdaonense strain:cgmcc 1.6134

Project description:Bacillus qingdaonensis CGMCC 1.6134 genome sequencing

| PRJNA303438 | ENA

Alkalicoccus daliensis strain:cgmcc 1.10369

Project description:Bacillus daliensis CGMCC 1.10369 genome sequencing

| PRJNA303439 | ENA

Glutamine synthetase gene glnA plays an important role in curdlan biosynthesis of Agrobacterium sp. CGMCC 11546

Project description:Purpose： The goal of this study is compare the effect of glnA gene in curdlan synthesis in Agrobacterium sp. CGMCC 11546. methods: The transcriptional and metabolomics analysis the function of glnA in Agrobacterium sp. CGMCC 11546. Results: The transcriptional and metabolomics showed that the decrease of curdlan production in the ΔglnA mutants may be caused by the insufficient supply of energy ATP conclusion: glnA play an important role in curdlan synthesis in Agrobacterium sp. CGMCC 11546

2022-06-30 | GSE153505 | GEO

Methionine biosynthetic pathway genes metH and metZ affect curdlan synthesis in Agrobacterium sp. CGMCC 11546

Project description:Purpose: The goal of this study is compare the effect of MetH and MetZ gene in curdlan synthesis in Agrobacterium sp. CGMCC 11546. methods: The transcriptional and metabolomics analysis the function of metH and metZ in Agrobacterium sp. CGMCC 11546. Results: The transcriptional and metabolomics showed that the decrease of curdlan production in the ΔmetH and ΔmetZ mutants may be caused by the insufficient supply of energy ATP conclusion: MetH and MetZ play an important role in curdlan synthesis in Agrobacterium sp. CGMCC 11546

2021-06-30 | GSE131215 | GEO

Bacillus velezensis strain:CGMCC 11640

Project description:Bacillus velezensis strain:CGMCC 11640 Genome sequencing

| PRJNA432489 | ENA

Transcriptomics analysis of Komagataeibacter europaeus CGMCC 20445 during acetic acid fermentation

Project description:We conducted transcriptome analysis of Komagataeibacter europaeus CGMCC 20445 samples under different acidity conditions to elucidate the changes in differentially expressed genes throughout the fermentation process.

2021-03-09 | GSE168432 | GEO

Bacillus tamaricis strain:CGMCC 1.15917

Project description:Bacillus tamaricis strain:CGMCC 1.15917 Genome sequencing and assembly

| PRJNA739830 | ENA

A Novel Nutrient Deprivation-Induced Neonicotinoid Insecticide Acetamiprid Degradation by Ensifer adhaerens CGMCC 6315

Project description:Proteomic Analysis. The proteomic expression of CGMCC 6315 under different nutrient concentration conditions was investigated by isobaric tags for relative and absolute quantitation (iTRAQ)-based quantitative proteomics. The CGMCC 6315 was cultured in LB broth and 1/15LB broth as described above, after which the strains were collected by centrifugation at 10,000× g for 10 min at 4°C. Protein extraction, digestion, iTRAQ labeling and peptide fractionation were performed using the protocol described by Jin et al. 29. Protein identification was conducted using a LC-20AD nano-HPLC instrument (Shimadzu, Kyoto, Japan) equipped with a Q EXACTIVE tandem mass spectrometer (Thermo Fisher Scientific, San Jose, CA, USA) for data-dependent acquisition detection by nano-electrospray ionization. The raw MS/MS data were converted into MGF format by the thermo scientific tool Proteome Discoverer, and the exported MGF files were searched using Mascot (version 2.3.02) against the selected database containing 7546 CGMCC 6315 coding genes. The IQuant software was used for quantitative analysis of the labeled peptides with isobaric tags. Fold changes of >1.7 with p-values <0.05 were used as a cut off for differentially regulated proteins.

2018-12-12 | PXD012014 | Pride

Bacillus licheniformis CGMCC 3963

Project description:Bacillus licheniformis CGMCC 3963 Genome sequencing and assembly

| PRJNA175351 | ENA