University of California

University of Illinois

Bp Corporation North America Inc.

N Louise Glass

James Harrison Doudna Cate

Chaoguang Tian

Huimin Zhao

Yong-Su Jin

William T Beeson, Iv

Suk-Jin Ha

Soo Rin Kim

Jing Du

Jin Ho Choi

Jonathan M Galazka

Sijin Li

Xiaomin Yang

Trent Russell Northen

James R Craig

Teresa Shock

Samuel Coradetti

Jens Heller

Lauren Jabusch

Peter Kim

Elizabeth A Znameroski

This disclosure provides systems, methods, and apparatus related to the determination of ecological processes. In one aspect, a device includes a base and a substrate in contact with a first side of the base. The base defines a stem port. The substrate and the first side of the base define a chamber. The chamber includes a root chamber and a first nutrient chamber. The root chamber and the first nutrient chamber are separated by a first mesh having openings of about 1 micron to 300 microns. The device is operable to house a plant, with roots of the plant being in the root chamber, and a stem of the plant passing through the stem port.

Devices for studying plant-fungus interactions and for imaging plant roots

The present disclosure provides mutant cells for the secretion of proteins and for the degradation of lignocellulosic biomass. Methods for the use of these cells are also provided. Specifically, the utility of combined genetic deletions of &#x3b2;-glucosidases and the catabolite repressor gene creA/cre-1 for protein secretion in fungal and yeast cells is disclosed.

Mutant cells for protein secretion and lignocellulose degradation

Provided herein are methods and compositions for increasing the production of one or more cellulases from a fungal host cell. The disclosure is based, on the surprising discovery that mis-expression of the transcriptional regulator clr-2 in a filamentous fungal cell was able to induce expression of cellulase genes under non-inducing or starvation conditions, resulting in increased secretion of cellulases from the cell. Advantageously, mis-expression of the transcription factor clr-2 in a filamentous fungal cell cultured in the absence of cellulose or cellobiose results in increased secretion of cellulases. The disclosure relates inter alia to a method of degrading cellulose-containing material, to a method of increasing the production of one or more cellulases from a fungal cell and to a method of reducing the viscosity of a pretreated biomass material, by contacting pretreated biomass material with a fungal host cell containing at least one recombinant nucleic acid encoding clr-2 or a related transcription factor.

Transcription factors for cellulosic enzyme production

The present disclosure relates to host cells containing a recombinant polynucleotide encoding a polypeptide where the polypeptide transports cellodextrin into the cell. The present disclosure further relates to methods of increasing transport of cellodextrin into a cell, methods of increasing growth of a cell on a medium containing cellodextrin, methods of co-fermenting cellulose-derived and hemicellulose-derived sugars, and methods of making hydrocarbons or hydrocarbon derivatives by providing a host cell containing a recombinant polynucleotide encoding a polypeptide where the polypeptide transports cellodextrin into the cell. The present disclosure relates to host cells containing a recombinant polynucleotide encoding a polypeptide where the polypeptide transports a pentose into the cell, methods of increasing transport of a pentose into a cell, methods of increasing growth of a cell on a medium containing pentose sugars, and methods of making hydrocarbons or hydrocarbon derivatives by providing a host cell containing a recombinant polynucleotide encoding a polypeptide where the polypeptide transports a pentose into the cell.

Methods and compositions for improving sugar transport, mixed sugar fermentation, and production of biofuels

Growing community of inventors

Berkeley, CA, United States of America

N Louise Glass