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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

ARG7 Arg7p

ARG7, Ornithine acetyltransferase
Top mentioned proteins: CAN, SET, ACID, Transcription Factor DP1, Enkephalin
Papers on ARG7
An improved ARS2-derived nuclear reporter enhances the efficiency and ease of genetic engineering in Chlamydomonas.
Mayfield et al., San Diego, United States. In Biotechnol J, Mar 2015
The improved arylsulfatase expression cassette was used to screen a new transgene promoter from the ARG7 gene, and found that the ARG7 promoter can express the ARS2 reporter as strongly as the HSP70-RBCS2 chimeric promoter that currently ranks as the best available promoter, thus adding to the list of useful nuclear promoters.
Improvement of L-citrulline production in Corynebacterium glutamicum by ornithine acetyltransferase.
Xu et al., Nanjing, China. In J Ind Microbiol Biotechnol, Feb 2015
To determine new strategies for further enhancement of L-citrulline production, the effect of L-citrulline on ornithine acetyltransferase (EC;
Studies on recombination processes in two Chlamydomonas reinhardtii endogenous genes, NIT1 and ARG7.
Slaninova et al., Bratislava, Slovakia. In Protist, 2013
In this study we compared two endogenous genes, NIT1 and ARG7, and their HR/NHR ratios when different types of fragments were used as donors of homologous sequences.
Improvement of L-arginine production by overexpression of a bifunctional ornithine acetyltransferase in Corynebacterium crenatum.
Xu et al., Wuxi, China. In Appl Biochem Biotechnol, 2011
Ornithine acetyltransferase (EC;
Isolation, characterization and long term preservation of mutant strains of Xanthophyllomyces dendrorhous.
Cifuentes et al., Santiago, Chile. In J Basic Microbiol, 2009
From a detailed analysis about the requirements of auxotrophic mutants the ARG7, ARG3 and PRO3 loci can be defined in this yeast.
Complementation of the Chlamydomonas reinhardtii arg7-8 (arg2) point mutation by recombination with a truncated nonfunctional ARG7 gene.
Slaninova et al., Regensburg, Germany. In Protist, 2007
Chlamydomonas reinhardtii arg7-8 (arg2) mutant strains carrying a hitherto undescribed mutation in their argininosuccinate lyase gene (ARG7) that leads to arginine auxotrophy have been used together with the corresponding wild-type gene as a very reliable transformation system since 1989.
Construction of modular tandem expression vectors for the green alga Chlamydomonas reinhardtii using the Cre/lox-system.
Zschoernig et al., Heidelberg, Germany. In Biotechniques, 2007
Tandem vectors carrying expression cassettes for Renilla luciferase and a metabolic selection marker (ARG7) were manufactured by fusing two plasmids in vitro using Cre/lox site-specific recombination.
Crystallization of ornithine acetyltransferase from yeast by counter-diffusion and preliminary X-ray study.
Zegers et al., Brussels, Belgium. In Acta Crystallogr Sect F Struct Biol Cryst Commun, 2007
The crystals belong to space group P4, with unit-cell parameters a = b = 66.98, c = 427.09 A, and a data set was collected to 2.76 A.
The LPB1 gene is important for acclimation of Chlamydomonas reinhardtii to phosphorus and sulfur deprivation.
Grossman et al., Stanford, United States. In Plant Physiol, 2005
The LPB1 gene was tagged by insertion of the ARG7 gene, which facilitated its isolation and characterization.
Insertional mutagenesis in a homologue of a Pi transporter gene confers arsenate resistance on chlamydomonas.
Tsuzuki et al., Hachiōji, Japan. In Plant Cell Physiol, 2003
An arsenate-resistant mutant AR3 of Chlamydomonas reinhardtii is a recessive mutant generated by random insertional mutagenesis using the ARG7 gene.
A Streptomyces rimosus aphVIII gene coding for a new type phosphotransferase provides stable antibiotic resistance to Chlamydomonas reinhardtii.
Hegemann et al., Saint Petersburg, Russia. In Gene, 2001
After addition of the 5'-region of hsp70A as a second promoter and insertion of the rbcS2 intron I, the transformation rate increased to two transformants per 1 x 10(5) cells, which is close to the efficiency of transforming auxotrophic strains with the homologous marker arg7.
Isolation and characterisation of chemotactic mutants of Chlamydomonas reinhardtii obtained by insertional mutagenesis.
Purton et al., Saint Petersburg, Russia. In Protist, 2000
The arginine-requiring strain arg7-8 was transformed with DNA carrying the wild-type ARG7 gene.
The yeast ARG7 gene product is autoproteolyzed to two subunit peptides, yielding active ornithine acetyltransferase.
Crabeel et al., Brussels, Belgium. In J Biol Chem, 2000
When artificially co-expressed from separate genes, the two subpeptides can complement an arg7 mutation; ornithine acetyltransferase activity is measurable.
The argininosuccinate lyase gene of Chlamydomonas reinhardtii: cloning of the cDNA and its characterization as a selectable shuttle marker.
Rochaix et al., Genève, Switzerland. In Mol Gen Genet, 1999
We describe the cDNA sequence for ARG7, the gene that encodes argininosuccinate lyase--a selectable nuclear marker--in Chlamydomonas reinhardtii.
Use of the ARG7 gene as an insertional mutagen to clone PHON24, a gene required for derepressible neutral phosphatase activity in Chlamydomonas reinhardtii.
Loppes et al., Liège, Belgium. In Mol Gen Genet, 1998
Twenty-four phoN mutants lacking the derepressible neutral (DN) phosphatase activity were isolated following transformation of the cw15arg7 strain with plasmid pASL harbouring the ARG7 gene encoding argininosuccinate lyase.
High-efficiency transformation of Chlamydomonas reinhardtii by electroporation.
Usuda et al., Hachiōji, Japan. In Genetics, 1998
Electroporation of strains CC3395 and CC425, cell wall-less mutants devoid of argininosuccinate lyase (encoded by ARG7), in the presence of the plasmid pJD67 (which contains ARG7) was used to optimize conditions for the introduction of exogenous DNA.
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