Abstract: Genes encoding microbial ?-glucuronidases and proteins and their uses are provided.

Abstract: Genes encoding microbial ?-glucuronidase and protein that is secreted and its uses are provided.

Abstract: Genes encoding microbial?-glucuronidases and proteins and their uses are provided.

Abstract: Clones containing a sequence encoding a glucuronide repressor are described. The nucleotide and amino acid sequences of a repressor (gusR) are presented. A glucuronide repressor is used to control expression of a transgene, detect glucuronides in a sample, and isolate glucuronides from a sample, among other uses.

Abstract: This invention relates generally to technologies for the transfer of nucleic acids molecules to eukaryotic cells. In particular non-pathogenic species of bacteria that interact with plant cells are used to transfer nucleic acid sequences. The bacteria for transforming plants usually contain binary vectors, such as a plasmid with a vir region of a Ti plasmid and a plasmid with a T region containing a DNA sequence of interest.

Abstract: This invention relates generally to technologies for the transfer of nucleic acids molecules to eukaryotic cells. In particular non-pathogenic species of bacteria that interact with plant cells are used to transfer nucleic acid sequences. The bacteria for transforming plants usually contain binary vectors, such as a plasmid with a vir region of a Ti plasmid and a plasmid with a T region containing a DNA sequence of interest.

Abstract: Genes encoding microbial &bgr;-glucuronidases and proteins and their uses are provided.

Abstract: Genes encoding microbial &bgr;-glucuronidases and proteins and their uses are provided.

Abstract: A continuous operation metering valve, based on true volumetric positive displacement technology, uses an innovative dual rack and drive pinion design that enables the valve to dispense from one meter chamber while the other meter chamber is filling. This provides greater dispense cycle rates because it does not require a fill or reload period. With an optional encoder-controlled motor, the inventive metering valve is capable of almost unlimited precision dispensing with “on-the-fly” adjustment capability. The metering valve is easily disassembled and cleaned, using stainless steel wetted path components and Teflon seals for the widest range of chemical compatibility. An integral electronic board, mounted to the side of the valve, may be utilized to control the 4-way directional valve and motor direction (when not using a rotary encoder control).

Abstract: Genes encoding microbial &bgr;-glucuronidase and protein that is secreted and its uses are provided.

Abstract: Clones containing a sequence encoding a glucuronide repressor are described. The nucleotide and amino acid sequences of a repressor (gusR) are presented. A glucuronide repressor is used to control expression of a transgene, detect glucuronides in a sample, and isolate glucuronides from a sample, among other uses.

Abstract: Clones containing a sequence encoding a glucuronide repressor are described. The nucleotide and amino acid sequences of a repressor (gusR) are presented. A glucuronide repressor is used to control expression of a transgene, detect glucuronides in a sample, and isolate glucuronides from a sample, among other uses.

Abstract: Genes encoding microbial &bgr;-glucuronidase and protein that is secreted and its uses are provided.

Abstract: Cellobiuronic acid may be prepared by hydrolysis of gellan. The method provides embodiments expressed in terms of amounts of cellobiuronic acid produced, amounts of gellan gum hydrolyzed and amounts of cellobiuronic acid present in fractions of a hydrolysate The method may further include isolation of a separated fraction of the hydrolysate where the separated fraction comprises cellobiuronic acid. A preferred embodiment of the method includes hydrolyzing gellan gum with a protic acid under reaction conditions that convert at least 95 wt.% of the gellan gum to a hydrolysate comprised of cellobiuronic acid and monosaccharides and isolating a separated fraction of the hydrolysate where cellobiuronic acid comprises at least a 95 wt.% of saccharides in the separated fraction.

Abstract: Cellobiuronic acid may be prepared by hydrolysis of gellan. The method provides embodiments expressed in terms of amounts of cellobiuronic acid produced, amounts of gellan gum hydrolyzed and amounts of cellobiuronic acid present in fractions of a hydrolysate The method may further include isolation of a separated fraction of the hydrolysate where the separated fraction comprises cellobiuronic acid. A preferred embodiment of the method includes hydrolyzing gellan gum with a protic acid under reaction conditions that convert at least 95 wt. % of the gellan gum to a hydrolysate comprised of cellobiuronic acid and monosaccharides and isolating a separated fraction of the hydrolysate where cellobiuronic acid comprises at least a 95 wt. % of saccharides in the separated fraction.

Abstract: Clones containing a sequence encoding a glucuronide repressor are described. The nucleotide and amino acid sequences of a repressor (gusR) are presented. A glucuronide repressor is used to control expression of a transgene, detect glucuronides in a sample, and isolate glucuronides from a sample, among other uses.

Abstract: The present invention relates to the .beta.-glucuronidase (GUS) gene fusion system, and to the cloning and characterization of the .beta.-glucuronidase and glucuronide permease genes of Escherichia coli. It is based on the surprising discovery that gene fusions comprising the .beta.-glucuronidase gene may be effectively expressed in a wide variety of organisms to produce active .beta.-glucuronidase enzyme. Because of the abundance and availability of useful substrates for .beta.-glucuronidase enzyme, GUS gene fusions may serve as a superior reporter gene system as well as an effective means of altering cellular phenotype. In conjunction with recombinant glucuronide permease, which may be used to render host cells permeable to .beta.-glucuronidase substrates, the GUS gene fusion system offers almost unlimited applications in the fields of plant and animal genetic engineering.

Abstract: The present invention relates to the .beta.-glucuronidase (GUS) gene fusion system, and to the cloning and characterization of the .beta.-glucuronidase and glucuronide permease genes of Escherichia coli. It is based on the surprising discovery that gene fusions comprising the .beta.-glucuronidase gene may be effectively expressed in a wide variety of organisms to produce active .beta.-glucuronidase enzyme. Because of the abundance and availability of useful substrates for .beta.-glucuronidase enzyme, GUS gene fusions may serve as a superior reporter gene system as well as an effective means of altering cellular phenotype. In conjunction with recombinant glucuronide permease, which may be used to render host cells permeable to .beta.-glucuronidase substrates, the GUS gene fusion system offers almost unlimited applications in the fields of plant and animal genetic engineering.

Abstract: The present invention relates to the .beta.-glucuronidase (GUS) gene fusion system, and to the cloning and characterization of the .beta.-glucuronidase and glucuronide permease genes of Escherichia coli. It is based on the surprising discovery that gene fusions comprising the .beta.-glucuronidase gene may be effectively expressed in a wide variety of organisms to produce active .beta.-glucuronidase enzyme. Because of the abundance and availability of useful substrates for .beta.-glucuronidase enzyme, GUS gene fusions may serve as a superior reporter gene system as well as an effective means of altering cellular phenotype. In conjunction with recombinant glucuronide permease, which may be used to render host cells permeable to .beta.-glucuronidase substrates, the GUS gene fusion system offers almost unlimited applications in the fields of plant and animal genetic engineering.