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Komagataeibacter medellinensis

ABSTRACT: Transcriptome analysis of Komagataeibater medellinensis NBRC 3288 and their thermally-adapted strains

PROVIDER: PRJDB12529 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	DRR326851_1.fastq.gz	Fastqsanger.gz
	DRR326851_2.fastq.gz	Fastqsanger.gz
	DRR326852_1.fastq.gz	Fastqsanger.gz
	DRR326852_2.fastq.gz	Fastqsanger.gz
	DRR326853_1.fastq.gz	Fastqsanger.gz

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Similar Datasets

Komagataeibacter medellinensis

Project description:Komagataeibacter medellinensis NBRC 3288 (thermally-adapted strain) genome sequencing project

| PRJDB12528 | ENA

Komagataeibacter medellinensis strain:NBRC 3288

Project description:Komagataeibacter medellinensis NBRC 3288 (cellulose producing adaptated strain) Whole Genome Sequencing Project

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Komagataeibacter medellinensis NBRC 3288

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Komagataeibacter medellinensis

Project description:Komagataeibacter medellinensis overview

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Komagataeibacter medellinensis NBRC 3288

Project description:Gluconacetobacter xylinus NBRC 3288 Genome sequencing project

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Komagataeibacter medellinensis strain:ID13488

Project description:Komagataeibacter medellinensis strain:ID13488 Genome sequencing and assembly

| PRJNA490026 | ENA

Expression analysis of Gluconacetobacter xylinus NBRC 3288 delta-fnrG mutant

Project description:Investigation of whole genome gene expression level changes in a Gluconacetobacter xylinus NBRC 3288 delta-fnrG mutant, compared to the wild-type strain.

2021-07-16 | GSE41775 | GEO

Acetobacter pasteurianus

Project description:Transcriptome analysis of Acetobacter pasteurianus SKU1108 and their thermally-adapted strains

| PRJDB15217 | ENA

Genome sequence and characterization of the bcs clusters for the production of nanocellulose from the low pH resistant strain Komagataeibacter medellinensis ID13488.

Project description:Komagataeibacter medellinensis ID13488 (formerly Gluconacetobacter medellinensis ID13488) is able to produce crystalline bacterial cellulose (BC) under high acidic growth conditions. These abilities make this strain desirable for industrial BC production from acidic residues (e.g. wastes generated from cider production). To explore the molecular bases of the BC biosynthesis in this bacterium, the genome has been sequenced revealing a sequence of 3.4 Mb containing three putative plasmids of 38.1 kb (pKM01), 4.3 kb (pKM02) and 3.3 Kb (pKM03). Genome comparison analyses of K. medellinensis ID13488 with other cellulose-producing related strains resulted in the identification of the bcs genes involved in the cellulose biosynthesis. Genes arrangement and composition of four bcs clusters (bcs1, bcs2, bcs3 and bcs4) was studied by RT-PCR, and their organization in four operons transcribed as four independent polycistronic mRNAs was determined. qRT-PCR experiments demonstrated that mostly bcs1 and bcs4 are expressed under BC production conditions, suggesting that these operons direct the synthesis of BC. Genomic differences with the close related strain K. medellinensis NBRC 3288 unable to produce BC were also described and discussed.

| S-EPMC6559206 | biostudies-literature

Effect of Different Carbon Sources on Bacterial Nanocellulose Production and Structure Using the Low pH Resistant Strain Komagataeibacter Medellinensis.

Project description:Bacterial cellulose (BC) is a polymer obtained by fermentation with microorganism of different genera. Recently, new producer species have been discovered, which require identification of the most important variables affecting cellulose production. In this work, the influence of different carbon sources in BC production by a novel low pH-resistant strain Komagataeibacter medellinensis was established. The Hestrin-Schramm culture medium was used as a reference and was compared to other media comprising glucose, fructose, and sucrose, used as carbon sources at three concentrations (1, 2, and 3% w/v). The BC yield and dynamics of carbon consumption were determined at given fermentation times during cellulose production. While the carbon source did not influence the BC structural characteristics, different production levels were determined: glucose > sucrose > fructose. These results highlight considerations to improve BC industrial production and to establish the BC property space for applications in different fields.

| S-EPMC5554020 | biostudies-other

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