Promoter sequence of 3-phosphoglycerate kinase gene 2 of...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

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C435S069100, C435S471000

Reexamination Certificate

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06528636

ABSTRACT:

FIELD OF THE INVENTION
The present invention is a promoter sequence of 3-phosphogycerate kinase gene 2 of lactic acid-producing fungus
Rhizopus oryzae
and a method of expressing a gene of interest in fungal species.
BACKGROUND OF THE INVENTION
The genus of Rhizopus is versatile in the production of biocatalysts such as glucoamylase and lipase and chemicals including L-(+)-lactic acid, fumaric acid, and ethanol. Rhizopus is the member of the order Mucorales, which is within the class Zygomycetes of the division Amastigomycota.
Rhizopus oryzae
(ATCC 9363) is the best lactic acid producer found in the Rhizopus genus, while
Rhizopus delemar
and
Rhizopus niveus
can produce significant amount of extracellular lipase. In addition,
R. oryzae
can also secrete large amount of glucoamylase in the solid culture for starch hydrolysis. Therefore,
R. oryzae
could be potentially a host for upgrading lactic acid production as well as foreign protein production. However, in the current literature, there is very limited information available on gene clones as well as gene regulatory elements (promoters) for
R. oryzae
. Less than nine gene clone and partial gene sequences are reported for
R. oryzae
, which include glucoamylase, ribosomal genes, and aspartic proteinase genes (GenBank Data Base).
The ability to genetically manipulate filamentous fungi largely depends on the successfulness to develop the transformation methods and gene expression systems. Transformation methods have been developed for filamentous fungi, in particular,
Aspergillus nidulans
and
Neurospora crassa
, including others such as
Aspergillus niger, Aspergillus oryzae, Penicillium nalgiovense
. To effectively direct the transcription or expression of an interested gene, strong gene regulating elements or promoters are required. These promoters can be isolated from the upstream sequences of strongly expressed gene clones. Phosphoglycerate kinase gene is one of the highly expressed genes found in yeast and filamentous fungi. This gene encodes some of the most abundant mRNA in the yeast cells, accounting for up to 5% of the total cellular protein expression. After the discovery and characterization of
Saccharomyces cerevisiae
gene, other phosphoglycerate kinase genes were also isolated from various fungal species such as
Penicillium chrysogenum
and
Rhizopus niveus
using
S. cerevisiae phosphoglycerate
kinase gene as homologous gene probe. However, only a few of phosphoglycerate kinase gene promoters were isolated and characterized, which were from
S. cerevisiae, Trichoderma reesei
, and
R. niveus
, among others.
To genetically manipulate
R. oryzae
, either for the purpose of metabolic pathway modification, conferring necessary traits such as acid tolerance and upgrading of lactic acid production, or producing biocatalyst of interest, high levels of mRNA expression are always desirable. Therefore, there is a need to isolate strong promoter sequences of
R. oryzae
and design/develop expression vectors, harboring the isolated phosphoglycerate kinase gene promoter.
SUMMARY OF THE INVENTION
The present invention provides the promoter clone discovery of phosphoglycerate kinase gene 2 of a lactic acid-producing filamentous fungal strain,
Rhizopus oryzae
. The isolated promoter can constitutively regulate gene expression under various carbohydrate conditions. In addition, the present invention also provides a design of an integration vector for the transformation of a foreign gene in
Rhizopus oryzae.


REFERENCES:
patent: 3247286 (1991-11-01), None
CR Soccol et al. “Production of L-Lactic Acid by Rhizopus Species”, p. 433-435, 1994, vol. 10, World Journal Microbiol. Biotechnol.
MJ Haas et al. “Cloning Expression and Characterization of a cDNA Encoding a Lipase From Rhizopus Delemar”, p. 107-113, 1991, Gene, vol. 109.
P Yin et al. “Enhanced Production of L(+)-Lactic Acid Corn Starch in a Culture of Rhizopus Oryzae Using an Air-Lift Bioreactor”, p. 249-253. 1997 J. Fermentation and Bioengineering, vol. 84.
P Van Solingen et al. “Sequence of the Penicillium Chrysogenum Phosphoglycerate Kinase Gene”, p. 11823, 1988 Nuc. Acids Res. vol. 16.
RA Hitzeman et al. “The Primary Structure of the Saccharomyces Cerevisiae Gene for 3-Phosphoglycerate Kinase”, p. 7791-7808. 1982 Nuc. Acids Res. vol. 10.
N Takaya et al. “Analysis of the 3-Phosphoglycerate Kinase 2 Promoter in Rhizopus Niveus”, p. 121-125. 1995 Gene, vol. 152.
S Vanhanen et al. “Promoter Structure and Expression of the 3-Phosphoglycerate Kinase-Encoding Gene (pgkl) of Trichoderma Reesei”, p. 129-133. 1991. Gene, vol. 106.
MJ Haas et al. “Lipases of the Genera Rhizopus and Rhizomucor: Versatile Catalysts in Nature and the Laboratory”, p. 549-588, 1994.
N Takaya et al. “Cloning and Characterization of Two 3-Phosphoglycerate Kinase Genes of Rhizopus Niveus and Heterologous Gene Expression Using Their Promoters”, p. 524-530. 1994. Curr. Genet. vol. 25.
DJ Ballance. “Transformation Systems for Filamentous Fungi and an Overview of Fungal Gene Structure”, p. 1-29. 1991.
MG Richey et al. “Transformation of Filamentous Fungi with Plasmid DNA by Electroporation”, p. 844-847. 1989. Phytopathology vol. 79.
M Kapoor. “Gene Transfer by Electroporation of Filamentous Fungi”, p. 279-289. 1996 in Methods in Molecular Biology, vol. 47.
MJ Holland et al. “isolation and Identification of Yeast Messenger Ribonuclide Acids Coding for Enolase, Glyceraldehyde-3-Phosphate Dehydrogenase, and Phosphoglycerate Kinase”, p. 4900-4907. 1978 Biochemistry, vol. 17.
J Mellor et al. “Efficient Synthesis of Enzymatically Active Calf Chymosin in Saccharomyces Cerevisiae”, p. 1-14. 1983 Gene, vol. 24.

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