Enhanced expression of proteolytic enzymes in koji mold

Chemistry: molecular biology and microbiology – Enzyme – proenzyme; compositions thereof; process for... – Hydrolase

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435183, 435195, 435212, 435219, 4352541, 43525411, 4352543, 4352548, 4352549, 435 691, 435 711, C12N 958

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060906073

DESCRIPTION:

BRIEF SUMMARY
TECHNICAL FIELD

The invention relates to genetic modifications of koji molds allowing enhanced expression of proteolytic enzymes.


BACKGROUND OF THE INVENTION

Hydrolyzed proteins, which are widely used in the food industry, may be prepared by hydrolysis of protein material with acid, alkali or enzymes. Various methods have been used koji molds for the preparation food products, which are hydrolyzed by action of a large variety of secreted amylases, proteinases and peptidases. Koji molds are those traditionally used for making a koji culture (U.S. Pat. No. 4,308,284) including cells of the genus Aspergillus, Rhizopus and/or Mucor, especially Aspergillus soyae, Aspergillus oryzae, Aspergillus phoenicis, Aspergillus niger, Aspergillus awamori, Rhizopus oryzae, Rhizopus oligosporus, Rhizopus japonicus, Rhizopus formosaensis, Mucor circinelloides, Mucor japanicus, Penicillium glaucum and Penicillium fuscum, for example.
According to the rules of the International Code of Botanical Nomenclature (ICBN), Aspergillus is an anamorphic genus. This means that true Aspergillus only reproduce asexually through conidiophores. However, the typical Aspergillus conidiophore morphology can also be found in fungi that can reproduce sexually via ascospores. Some Aspergillus taxonomists caused confusion, because they did not adhere to ICBN terminology. Instead, they attempted to make various revisions of taxonomical schemes to include Aspergillus nidulans in this genus, despite the fact that its taxonomically correct name is Emericelia nidulans (Samson, In: Aspergillus. Biology and Industrial Applications, pp 355-390, Ed. by Bennett and Klich, Boston)
EP417481 (Societe des Produits Nestle) thus describes a process for the production of a fermented soya sauce, in which a koji is prepared by mixing a koji culture with a mixture of cooked soya and roasted wheat, the koji is then hydrolyzed in aqueous suspension for 3 to 8 hours at 45.degree. C. to 60.degree. C. with the enzymes produced during fermentation of the koji culture, a moromi is further prepared by adding sodium chloride to the hydrolyzed koji suspension, the moromi is left to ferment and is then pressed and the liquor obtained is pasteurized and clarified.
EP429760 (Societe des Produits Nestle) describes a process for the production of a flavoring agent in which an aqueous suspension of a protein-rich material is prepared, the proteins are solubilized by hydrolysis of the suspension with a protease at pH6.0 to 11.0, the suspension is heat-treated at pH 4.6 to 6.5, and the suspension is ripened with enzymes of a koji culture.
Likewise, EP96201923.8 (Societe des Produits Nestle) describes a process for the production of a meat flavor, in which a mixture containing a vegetal proteinaceous source and a vegetal carbohydrates containing source is prepared, said mixture having initially at least 45% dry matter, the mixture is inoculated with a koji culture and by one or more another species of microorganisms involved in the traditional fermentation of meat, and the mixture is incubated until meat flavors are formed.
However, on the one hand, acid or alkaline hydrolysis can destroy the essential amino acids produced during hydrolysis thus reducing the nutritional value, whereas enzymatic hydrolysis rarely goes to completion so that the hydrolyzed protein contains substantial amounts of peptides. The optimization and further development of koji processes have been seriously hampered by the lack of knowledge on the nature of the hydrolytic enzymes, their regulation and how process parameters affect their expression and activity (e.g. temperature, pH, water activity, and salt concentration).
In the fungal Emericella nidulans (Katz et al., Gene, 150, 287-292, 1994), fermentation activity is subject to at least three general control circuits including carbon catabolite repression, nitrogen and sulfur metabolite repression. These three regulatory circuits ensure that the available nitrogen-, carbon-, and sulfur sources in a substrate are utilized sequentially according to their ni

REFERENCES:
patent: 4308284 (1981-12-01), Noda et al.
Kudla et al. The EMBO Journal. vol. 9(5), pp. 1355-1364, 1990.
Stankovich et al. Molecular Microbiology. vol. 7(1), pp. 81-87, 1993.
Kudla, Bernard et al. XP000615427. "The regulatory gene areA mediating nitrogen metabolite repression in Aspergillus nidulans. Mutations affecting specificity of gene activation alter a loop residue of a putative zinc finger". The EMBO Journal vol. 9 No. 5 pp. 1355-1364, 1990.
Stankovich, M. et al. XP002048815. "C-terminal truncation of the transcriptional activator encoded by areA in Aspergillus nidulans results in both loss-of-function and gain-of-function phenotypes". Molecular Microbiology (1993) 7(1) pp. 81-87.
Platt, Adam et al. XP002077390. "Nitrogen metabolite signaling involves the C-terminus and the GATA domain of the Aspergillus transcription factor AREA and the 3 ' untranslated region of its mRNA". The EMBO Journal vol. 15 No. 11 pp. 2791-2801, 1996.
van den Hombergh, Johannes, P.T.W. et al. XP002048806. "Aspergillus as a host for heterologous protein production: the problem of proteases". Tibtech Jul. 1997 (vol. 15). pp. 256-263.
Jarai, G. et al. XP002077528. Abstract for "Nitorgen, carbon, and pH regulation of extracellular acidic proteases of Aspergillus niger". Current Genetics 26 (3). 1994. pp. 238-244.
XP 002048808. Abstract for "Enzyme compositions useful preparation hydrolysis food protein contain prolyl endo peptidase obtain mircrobe pseudomonas species". May 9, 1995.

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