C12N1/145

BIOLOGICAL CONTROL AGENT FORMULATIONS INCLUDING TRICHODERMA

The present disclosure relates to formulations including Trichoderma isolates, as well as methods thereof. In particular embodiments, the formulation can include one or more Trichoderma isolates, in which the formulation can include solid carriers and/or liquid carriers. Such formulations can be useful for treating or protecting plants, as well as counteracting growth of pathogenic organisms in proximity to the plant.

Hybrid mycelial cellulose sheet and preparation thereof

A leather-like hybrid mycelial cellulose sheet and production thereof. Precise selection of mushroom species and reagents allows for production at low pH, thereby resulting in a strong, flexible, and dry leather-like material suitable for application in various industries.

METHODS OF INCREASING THE GERMINATION RATE OF FUNGAL SPORES
20220312776 · 2022-10-06 ·

The present invention relates to a method of increasing the germination rate of spores of a fungal microorganisms formulated in a liquid composition essentially free of water, comprising, prior to applying to a plant, plant part or locus where a plant is growing or intended to be grown, suspending said composition in an agriculturally acceptable water-based liquid in a ratio of liquid composition and water-based liquid of between 1000:1 and 1:10. The invention further relates to a method of increasing efficacy of a biological control agent based on spores of a fungal microorganisms and a method of controlling the quality of such biological control agents.

RECOMBINANT FUNGAL STRAINS WITH REDUCED LEVELS OF MYCOTOXINS
20220315881 · 2022-10-06 ·

Described herein are recombinant edible filamentous fungal strain comprising a genetic modification of a gene in a mycotoxin biosynthesis pathway and methods to produce such recombinant edible filamentous fungal strains. Such recombinant strains comprise reduced levels of mycotoxins. Also described are food materials comprising the recombinant edible filamentous fungal strains described herein, and methods to prepare them.

INDOLE DITERPENE BIOSYNTHESIS

The present invention generally relates to methods of producing one or more indole diterpene compounds in the epoxy janthitrem biosynthetic pathway and polynucleotides, polypeptides, expression constructs and host cells useful in the production of one or more indole diterpene compounds, and methods of using same to confer a benefit to an organism, such as increased insect pest resistance.

FILAMENTOUS FUNGAL BIOMATS, METHODS OF THEIR PRODUCTION AND METHODS OF THEIR USE
20230141365 · 2023-05-11 ·

A novel method of growing fungi is disclosed which uses an engineered artificial media and produces high density filamentous fungi biomats that can be harvested with a minimum of processing and from which fungal products such as antibiotics, proteins, and lipids can be isolated, the method resulting in lowered fungus cultivation costs for energy usage, oxygenation, water usage and waste stream production.

OLEAGINOUS YEAST VARIANT, METHOD FOR OBTAINING THEREOF AND USE THEREOF FOR LIPID PRODUCTION

The present invention concerns an oleaginous yeast variant of the species Rhodosporidium azoricum characterized by higher biomass yields and intra- cellular lipid accumulation useful for the production of bio-fuels higher, in determined conditions, with respect to the wild type strain of the same species. Furthermore, the invention concerns a method through which said oleaginous yeast variant of the species Rhodosporidium azoricum was obtained. The invention further concerns the lipid production by means of said variant strain of oleaginous yeast of the species Rhodosporidium azoricum.

HIGHLY EFFICIENT ETHANOL-FERMENTATIVE YEAST
20170369906 · 2017-12-28 ·

A highly efficient ethanol-fermentative yeast having high efficiency in ethanol production is provided without introducing a foreign gene. The highly efficient ethanol-fermentative yeast features a fermentative yeast effectively producing ethanol from pentose and hexose and being deposited to NITE Patent Microorganisms Depositary under the accession number NITE BP-01963.

BIPOLARIS YAMADAE (Y. NISIK.) SHOEMAKER, AND SCREENING AND IDENTIFICATION METHOD THEREFOR AND USE THEREOF
20230203429 · 2023-06-29 · ·

A Bipolaris yamadae (Y. Nisik.) shoemaker (HXDC-1-2), and a screening and identification method therefor and use thereof. The Bipolaris yamadae (Y Nisik.) strain (HXDC-1-2) is deposited in the China General Microbiological Culture Collection Center with the accession number CGMCC No. 17778. The Bipolaris yamadae (Y. Nisik.) strain (HXDC-1-2) is applied to biological weed control when the conidial concentration is 10.sup.2 conidia/ml or more.

TRANSFORMANT AND ITS PRODUCTION PROCESS, AND METHOD FOR PRODUCING LACTIC ACID
20170356017 · 2017-12-14 ·

Provided is a transformant which can produce lactic acid with a high productivity without requiring neutralization with an alkali and is excellent in both of lactic acid production capability and growth ability and its production process, and a method for producing lactic acid by using the transformant.

A transformant containing from 3 to 5 copies of a lactate dehydrogenase gene derived from human and introduced into a Schizosaccharomyces pombe host, wherein a gene that is a part of a group of genes encoding pyruvate decarboxylase of the Schizosaccharomyces pombe host is deleted or inactivated. A transformant characterized by providing a cell concentration of at least 4.0 g (on a dry cell weight basis)/L of a culture broth prepared by inoculating cells, at an initial cell concentration of 0.04 g (on a dry cell weight basis)/L, into a 500 mL Sakaguchi flask containing 100 mL of a liquid culture broth which includes 1% of yeast extract, 2% of peptone and 6% of glucose, and then cultivating 20 hours at a temperature of 32° C. under shaking conditions of 110 rpm and 7 cm stroke, and providing a lactic acid concentration of at least 80 g/L of a fermentation liquor prepared by inoculating cells obtained by cultivating 20 hours under the above-described conditions, at an initial cell concentration of 36 g (on a dry cell weight basis)/L, into a 11.1% glucose aqueous solution, and then fermenting 3 hours at a temperature of 32° C. under shaking conditions of 110 rpm and 7 cm stroke. A method for producing lactic acid by using these transformants.