Title |
Glyco-Engineering
|
---|---|
Published by |
Methods in molecular biology, January 2015
|
DOI | 10.1007/978-1-4939-2760-9 |
Pubmed ID | |
ISBNs |
978-1-4939-2759-3, 978-1-4939-2760-9
|
Authors |
Alexandra Castilho, Jaffé, Stephen R P, Strutton, Benjamin, Pandhal, Jagroop, Wright, Phillip C |
Editors |
Alexandra Castilho |
Abstract |
Inverse metabolic engineering (IME) provides a strategy to rapidly identify the genetic elements responsible for the desired phenotype of a chosen target organism. This methodology has been successfully applied towards enhancing the N-linked glycosylation efficiency of Escherichia coli. Here, we describe the generation of differentially sized libraries from the E. coli W3110 genome followed by high-throughput semiquantitative glycan specific screening. DNA sequenced targets demonstrating increased levels of glycan production were selected for forward engineering, protein overexpression, and absolute quantification of glycoproteins. |
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Mendeley readers
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Student > Ph. D. Student | 25 | 19% |
Researcher | 20 | 15% |
Student > Bachelor | 17 | 13% |
Other | 7 | 5% |
Other | 14 | 11% |
Unknown | 23 | 17% |
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Chemistry | 7 | 5% |
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Other | 8 | 6% |
Unknown | 23 | 17% |