Literature DB >> 17951635

Saturation of the secretory pathway by overexpression of a hookworm (Necator americanus) Protein (Na-ASP1).

Mehmet Inan1, Sarah A Fanders, Wenhui Zhang, Peter J Hotez, Bin Zhan, Michael M Meagher.   

Abstract

Human hookworm infection is one of the most significant parasitic infections, and a leading global cause of anemia and malnutrition of adults and children in rural areas of the tropics and subtropics. Necator americanus secretory protein (Na-ASP1), which is a potential vaccine candidate against hookworm infections, has been expressed in Pichia pastoris. Na-ASP1 protein was expressed extracellulary by employing the leader sequence of the alpha-mating factor of Saccharomyces cerevisiae. Most of the protein produced by single copy clones was secreted outside the cell. The Na-ASP1 steady state mRNA levels of the clones were correlated to their Na-ASP1 gene copy number. However, increasing gene copy number of Na-ASP1 protein in P. pastoris saturated secretory capacity and therefore, decreased the amount of secreted protein in clones harboring multiple copies of Na-ASP1 gene.

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Year:  2007        PMID: 17951635     DOI: 10.1007/978-1-59745-456-8_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  6 in total

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Journal:  Folia Microbiol (Praha)       Date:  2017-03-09       Impact factor: 2.099

4.  Recent advances on the GAP promoter derived expression system of Pichia pastoris.

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5.  Heterologous expression of recombinant urate oxidase using the intein-mediated protein purification in Pichia pastoris.

Authors:  Reihaneh Khaleghi; Sedigheh Asad
Journal:  3 Biotech       Date:  2021-02-08       Impact factor: 2.406

6.  Improving the secretion of a methyl parathion hydrolase in Pichia pastoris by modifying its N-terminal sequence.

Authors:  Ping Wang; Lu Huang; Hu Jiang; Jian Tian; Xiaoyu Chu; Ningfeng Wu
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  6 in total

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