Plasmids yeast

Yeast. The advantages of expression in yeast include potentially high level production of proteins, the abiUty to have expressed proteins secreted into the media for ease of purification, and relatively low cost, easy scale-up. A disadvantage is that plasmid instabiUty may be a problem which can lead to low product yield. Whereas post-translational modification occurs in yeast, proteins are quite often hyperglycosylated. This is generally a problem with expression in Saccharomyces cerevisiae but not for the more recently used yeast host Pichiapastoris (25) (see Yeasts). 

The test system was considerably less sensitive to endosulfan when mouse ER, rather than human ER, was used to mediate (3-gal activity (Ramamoorthy et al. 1997). In similar assays, endosulfan at 10 jM had no effect on (3-gal activity in yeast Saccharomyces) transfected with either the human or rainbow trout ER (Andersen et al. 1999). In addition, no effect was observed on transcriptional activation of HeLa cells transfected with plasmids containing an estrogen receptor as a responsive element (Shelby et al. 1996). Endosulfan also did not induce transient reporter gene expression in MCF-7 human breast cancer cells at an incubation concentration of 2.5 pM (Andersen et al. 1999). Maximum endosulfan-induced ER-mediated luciferase reporter gene expression occurred in vitro in a T47D human breast adenocarcinoma cell line at approximately 10 pM, while 50% expression of luciferase occurred at about 5.9 pM the maximum expression was approximately 59% of the effect from exposure to 0.03 nM estradiol (0.00003 pM) (Legler et al. 1999). Luciferase expression from combined treatment with endosulfan and dieldrin was additive over concentrations ranging from 3 to 8 pM. 

In the biosynthetic approach, protein expression in E. coli [27], yeast [28, 29], and plants [30, 31] have been employed. This approach requires the construction of genes encoding for these repetitive polypeptides. Different methods for gene construction have been pubhshed multimerization [32], recursive directional ligation [33], and recursive directional ligation via plasmid reconstruction [23, 34]. 

Transgenic E. coli accumulate comparatively low levels of carotenoids " compared to microbial algae, yeasts, and bacteria. Many efforts ° have focused on increasing accumulation by manipulation of factors affecting metabolic flux and metabolite accnmnlation (listed and discnssed in Sections 5.3.1.1 and 5.3.1.3 A) and have been reviewed." - " In bacterial systems, approaches to control can be categorized as either infrastructural (plasmids, enzymes, strains) or ultrastructural (media and feeding, enviromnent, precursor pools, substrate flux). 

Each of the -6000 PCR products was then co-transformed into yeast along with the recipient vector that had been linearized using a restriction enzyme that digests the plasmid at the desired cloning site. The 70 bp of homologous flanking sequence on each end of the PCR products is sufficient for the yeast homologous recombination system to act upon and insert the PCR product into the vector (Hudson et al., 1997 Ma et al., 1987). 

Plasmids are small, circular DNAs that range in size from 2 to approximately 100 kb. They also can be amplified to approximately 20 copies per cell. In addition, plasmids can be introduced into bacterial cells, although less efficiently than phage vectors. Some plasmids can be used to introduce recombinant DNA into yeast cells. 

Yeast-bacteria shuttle plasmids are usually able to be maintained in both E. coli and yeast and can be episomal or integrated into the host genome. First, plasmid DNA is usually amplified in E. coli before yeast gets transformed. Different antibiotic resistance cassettes are available, and also an abundance of autotrophic markers was established. 

Bacteria normally harbour a single, circular chromosome that tends to be tethered to the bacterial plasma membrane and tends to have few if any closely associated proteins. Many bacteria also contain extra-chromosomal DNA in the form of plasmids, as will be discussed later. Eukaryotes (plants, animals and yeasts) posses multiple linear chromosomes contained within a cell nucleus, and these chromosomes are normally closely associated with proteins termed histones (the pro-tein-DNA complex is termed chromatin). Eukaryotes also invariably possess DNA sequences within mitochondria and in chloroplasts in plants. The (usually circular) DNA molecules are much... 

To meet the infectivity requirement in the definition of a prion, the abnormal form of the protein must be transmissible to other cells and organisms of the same species. In yeast and filamentous fungi, infectious agents such as viruses and plasmids are naturally transmitted by cytoplasmic mixing during mating or heterokaryon formation (Wickner, 2001). 

Walker and Dhurjati1421 have used culture fluorescence for on-line discrimination of host and plasmid-carrying strains of Escherichia coll In addition, culture fluorescence has also been used in the control of fed-batch fermentation on yeast cell production/29, 431... 

Technically, cDNAs are cloned into plasmids carrying an antibiotic selection marker for propagation in bacteria, a nutritional selection marker for selection of transfected yeast as well as the respective origins of replication. After amplification in bacteria, the plasmids are transfected into the corresponding auxothrophic yeast strain using similar methods as for bacteria and stably... 

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