Study on the molecular basis of glucoamylase overproduction of a mutant strain Aspergillus niger T21

Science in China, Series C: Life Sciences

Volumn 44, Issue 3, 2001, Pages 287-293

  Xiaochun, F ^a   Runxiang, Q ^a   Li, L ^a   Guomin, T ^a  

^a INSTITUTE OF MICROBIOLOGY   (China)

Author keywords

Aspergillus niger; Deletion analysis; Glucoamylase; Promoter activity comparison

Indexed keywords

GENES; MOLECULAR BIOLOGY; MUTAGENS; RNA;

GLUCOAMLYASE;

GLUCOSE;

ASPERGILLUS NIGER;

EID: 0034940289     PISSN: 10069305     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf02879335     Document Type: Article

References (13)

1. The overall analysis and comparison of the expression of glucoamylase in the overproduction strain A. niger T21 and its original strain A. niger 3.795
2. Cloning, sequencing and comparison of the 5′-flanking regions of glaA gene from high and low glucoamylase producing strains of Aspergillus niger
3. Cloning and sequencing of glucoamylase gene from Aspergillus niger 3:795
4. Cotransformation of glucoamylase overproducing strain Aspergillus niger T21 with niaD and uidA gene
5. Expression of the Escherichia coli β-glucuronidase gene in industrial and phytopathogenic filamentous fungi
6. Protein measurement with the folin phenol reagent
7. Isolation of genomic DNAs from fungi using benzyl chloride
8. A small-scale procedure for the rapid isolation of plant RNAs
9. Improved transformation efficiency of Aspergillus niger using the homologous niaD gene for nitrate reductase
10. Regulation of the glaA gene of Aspergillus niger
11. The effect of multiple copies of the upstream region on expression of the Aspergillus niger glucoamylase-encoding gene
12. Aspergillus nidulans nuclear proteins bind to a CCAAT element and the adjacent upstream sequences in the promoter region of the starch-inducible Taka-amylase A gene
13. Functional elements of the promoter region of the Aspergillus oryzae glaA gene encoding glucoamylase