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Items: 1 to 20 of 1022

1.

Compare transcriptome profile of reference strain and mutant of HapX during A.niger grown on maltose

(Submitter supplied) Transcriptome analysis was performed to identify the differentially expressed genes between hapX mutant and reference strains during their growth on maltose
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21721
4 Samples
Download data: XLS
Series
Accession:
GSE260627
ID:
200260627
2.

The pleiotropic phenotype of FlbA of Aspergillus niger is explained in part by the activity of seven of its downstream-regulated transcription factors.

(Submitter supplied) Aspergillus niger fulfills an important role in nature in nutrient cycling and is a main cell factory for the industrial production of metabolites and enzymes. Inactivation of flbA in A. niger results in thinner cell walls, increased cell lysis, abolished sporulation, and an increased secretome complexity. A total of 36 transcription factor genes are differentially expressed in ∆flbA. Here, seven of these genes (abaA, aslA, aslB, azf1, htfA, nosA, and srbA) were inactivated. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34135
9 Samples
Download data: TSV, XLSX
Series
Accession:
GSE254305
ID:
200254305
3.

Differential expression analysis of Aspergillus niger genes in mRMA level between in seed medium and fermentation media for L-malic acid production

(Submitter supplied) Generally, A. niger undergoes two steps consisting of seed stage and fermentation stage to synthesize malic acid. However, it remains unknown which metabolic pathways, regulators, and key genes respond to the transition from seed medium to fermentation medium. In this study, we obtained the total mRMA of a high L-malate-yielding strain A. niger RG0095 at seed stage and fermentation stage, respectively, and performed a global differential expression analysis.
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32288
6 Samples
Download data: TXT
Series
Accession:
GSE235528
ID:
200235528
4.

Regulation of inulin and sucrose utilization by Aspergillus niger AmyR and InuR

(Submitter supplied) The aim of this study was to investigate the regulatory role of Aspergillus niger AmyR and InuR during growth on inulin and sucrose
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32288
24 Samples
Download data: TSV, TXT
Series
Accession:
GSE204768
ID:
200204768
5.

Metabolic engineering reveals the relative importance of different sugar catabolic pathways during growth of Aspergillus niger on plant biomass

(Submitter supplied) To evaluate the relative contribution of individual sugar catabolic pathways to the overall physiology of A. niger during growth on plant biomass, the A. niger sugar catabolic pathways involved in converting the most common monomers of plant biomass polysaccharides were blocked, and the phenotype as well as the transcriptomic response of these single-pathway deletion mutants was analysed on two distinct plant biomass substrates: wheat bran (WB) and sugar beet pulp (SBP). more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31925
84 Samples
Download data: TXT
Series
Accession:
GSE196397
ID:
200196397
6.

Identification of three enzymes of the vanillin and vanillic acid metabolic pathway in the filamentous fungi Aspergillus niger

(Submitter supplied) The aim of this study was to find candidate genes in A. niger involved in the vanillic acid metabolic pathway.
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25519
8 Samples
Download data: TXT
Series
Accession:
GSE154865
ID:
200154865
7.

Comparative study of gene expression in Aspergillus niger solid and submerged growth during sugar beet pulp utilization

(Submitter supplied) In this study, we compared the gene expression pattern of A. niger grown in liquid sugar beet pulp (SBP) at different time points, a by-product of the sugar industry that consists mainly of cellulose, xyloglucan, and pectin. Finally, we compared A. niger genetic response to liquid SBP to that of the same fungus when grown on solid SBP plates and polygalacturonic acid (PGA).
Organism:
Aspergillus niger; Aspergillus niger CBS 513.88
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL6758
8 Samples
Download data: CEL, TXT
Series
Accession:
GSE175954
ID:
200175954
8.

Re-routing of sugar catabolism provides a better insight into fungal flexibility in using plant biomass-derived monomers as substrates

(Submitter supplied) The filamentous ascomycete Aspergillus niger has received increasing interest as a cell factory, being able to efficiently degrade plant cell wall polysaccharides as well as having an extensive metabolism to convert the released monosaccharides into value added compounds. The pentoses D-xylose and L-arabinose are the most abundant monosaccharides in plant biomass after D-glucose, being major constituents of xylan, pectin and xyloglucan. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21818
90 Samples
Download data: TXT
Series
Accession:
GSE162901
ID:
200162901
9.

The molecular response of Aspergillus niger to guar gum

(Submitter supplied) Guar gum consists mainly of galactomannan, and constitutes the endosperm of guar seeds that acts as a reserve polysaccharide for germination. Due to its molecular structure and physical properties, this biopolymer has been considered as one of the most important and widely used gums in industry. However, for many of these applications this (hemi-)cellulosic structure needs to be modified or (partially) depolymerized in order to customize and improve its physicochemical properties. more...
Organism:
Aspergillus niger; Aspergillus niger CBS 513.88
Type:
Expression profiling by array
Platform:
GPL6758
16 Samples
Download data: CEL
Series
Accession:
GSE119310
ID:
200119310
10.

Deletion of the Aspergillus niger pro-protein processing protease gene kexB results in a pH-dependent morphological transition during submerged cultivations and increases cell wall chitin content

(Submitter supplied) There is a growing interest for the use of post-fermentation mycelial waste to obtain cell wall chitin as an added-value product. In the pursuit to identify suitable production strains that can be used for post-fermentation cell wall harvesting, we turned to an Aspergillus niger strain in which the kexB (also named pclA in literature) gene was deleted. Previous work has shown that deletion of kexB causes hyper-branching and thicker cell walls, which is beneficial as these properties reduce fermentation viscosity and lysis. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25519
4 Samples
Download data: TSV
Series
Accession:
GSE151618
ID:
200151618
11.

Evolutionary adaptation of Aspergillus niger for increased ferulic acid tolerance

(Submitter supplied) The aim of this study was to find candidate genes in A. niger involved in the increase tolerance against ferulic acid in A. niger Fa6
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21721
8 Samples
Download data: TXT
Series
Accession:
GSE135001
ID:
200135001
12.

Discovery and characterization of a novel p-hydroxybenzoate-m-hydroxylase, protocatechuate 3,4 ring-cleavage dioxygenase and hydroxyquinol 1,2 ring-cleavage dioxygenase from Aspergillus niger

(Submitter supplied) The aim of this study was to find candidate genes in A. niger involved in the degradation of benzoic acid.
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21721
10 Samples
Download data: TXT
Series
Accession:
GSE134999
ID:
200134999
13.

Omics analysis with modeling reveals global adaptation of Aspergillus niger to hypoxic condition

(Submitter supplied) Oxygen limitation is regarded as a useful strategy to improve enzyme production by mycelial fungus like Aspergillus niger. However, the intracellular metabolic response of A. niger to oxygen limitation is still obscure. To address this, the metabolism of A. niger was studied using multi-omics integrated analysis based on the latest GEMs (genome-scale metabolic model), including metabolomics, fluxomics and transcriptomics. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21721
11 Samples
Download data: XLS
Series
Accession:
GSE109525
ID:
200109525
14.

A seven-membered cell wall related transglycosylase gene family in Aspergillus niger is relevant for cell wall integrity in cell wall mutants with reduced α-glucan or galactomannan

(Submitter supplied) Chitin is an important fungal cell wall component that is cross-linked to β-glucan for structural integrity. Acquisition of chitin to glucan cross-links has previously been shown to be performed by transglycosylation enzymes in S. cerevisiae, called Congo Red hypersensitive (Crh) enzymes. Here, we characterized the impact of deleting all seven gene members of the crh gene family (crhA-G) in Aspergillus niger on cell wall integrity, cell wall composition and genome-wide gene expression. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21090
8 Samples
Download data: TXT
Series
Accession:
GSE142461
ID:
200142461
15.

An Aspergillus niger colony locally adapts its molecular responses to spatially separated substrates

(Submitter supplied) Saprotrophic fungi, such as Aspergillus niger, grow as mycelial colonies that are often considered uniform entities. To test this uniformity, we analyzed pie-slice sections of a colony grown on spatially separated substrates (glucose, wheat bran, sugar beet pulp) using transcriptomics, proteomics and metabolomics. The colony tuned its response to the local carbon source composition. Plant biomass degrading CAZymes and intracellular carbon catabolic enzymes were more abundant in parts of the colony containing the corresponding sugars. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25482
27 Samples
Download data: TXT
Series
Accession:
GSE118894
ID:
200118894
16.

Comparative transcriptomics of Aspergillus niger when deleted or overexpressed for the putative transcription factors MjkA, MjkB and the histon deactelyase HdaX

(Submitter supplied) Purpose: Expression profiling of two ORFs encoding putative transcription factors: An07g07370 (TF1/MjkA) and An12g07690 (TF2/MjkB), and a histone deacetylase (An09g06520, HdaX) under carbon-limited batch cultivations (biological duplicate runs) in Aspergillus niger. Methods: Single deletion strains for TF1, TF2 and HD, respectively, (ii) a double deletion strain for TF1 and TF2, and (iii) individual conditional overexpression mutants for TF1, TF2 and HD using the Tet-on system were analysed. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25519
28 Samples
Download data: TXT
Series
Accession:
GSE119311
ID:
200119311
17.

Deletion of the FlbA-regulated transcription factor msnB of Aspergillus niger affects protein secretion

(Submitter supplied) Colonies of Aspergillus niger secrete proteins throughout the colony except for the sporulating zone. Strains in which the sporulation gene flbA is deleted do not reproduce asexually and secrete proteins throughout the mycelium. Moreover, ΔflbA hyphae lyse and have thinner cell walls. This pleiotropic phenotype is associated with differential expression of 36 transcription factor genes, of which msnB was inactivated in this study. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21818
6 Samples
Download data: TXT
Series
Accession:
GSE104669
ID:
200104669
18.

The FlbA-regulated predicted transcription factor rpnR of Aspergillus niger is involved in protein secretion and stress resistance

(Submitter supplied) Proteins are secreted throughout the mycelium of Aspergillus niger except for the sporulating zone. Inactivation of flbA results in colonies that do not reproduce asexually and secrete proteins throughout the colony. Moreover, ΔflbA hyphae lyse and have thinner cell walls. This pleiotropic phenotype is associated with differential expression of 38 transcription factor genes, of which rpnR was inactivated in this study. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21818
6 Samples
Download data: TXT
Series
Accession:
GSE102899
ID:
200102899
19.

The fungus Aspergillus niger consumes sugars in a sequential manner that is not mediated by the carbon catabolite repressor CreA

(Submitter supplied) Aspergillus niger is a filamentous ascomycete fungus that is commonly found in most biotopes around the globe. In nature, A. niger degrades the plant biomass polysaccharides to monomeric sugars, transports them into the cells, and uses a variety of catabolic pathways to convert them into biochemical building blocks and energy. We show that when grown in liquid cultures, A. niger takes up plant-biomass derived monomeric sugars (and maltose) in a highly sequential manner, rather than simultaneously. more...
Organism:
Aspergillus niger; Aspergillus niger CBS 513.88
Type:
Expression profiling by array
Platform:
GPL6758
8 Samples
Download data: CEL
Series
Accession:
GSE98434
ID:
200098434
20.

The FlbA-regulated transcription factor FusR of Aspergillus niger is involved in production of fumonisin

(Submitter supplied) Colonies of Aspergillus niger secrete proteins throughout the colony except for the sporulating zone. Inactivation of flbA results in colonies that are unable to reproduce asexually and that secrete proteins throughout the mycelium. In addition, the ΔflbA strain shows cell lysis and has thinner cell walls. This pleiotropic phenotype is associated with differential expression of 38 transcription factor genes. more...
Organism:
Aspergillus niger
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21090
4 Samples
Download data: DIFF
Series
Accession:
GSE93990
ID:
200093990
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