Web(CDRs) were constructed by spiked mutagenesis using degenerate oligonucleotides and transformed into yeast strain BJ5465 (ATCC, VA, USA, no. 208289) using lithium acetate as described [16]. Libraries were induced and screened for improved binders using fluorescence-assisted cell sorting on a FACSAria cell sorter (BD Biosciences, WebMay 1, 2000 · This plasmid DNA was subsequently used for transformation into S.cerevisiae BJ 5465 as described above. Single colonies were picked from YNB plates and grown at …
Saccharomyces Genome Database SGD
WebMar 1, 2024 · Yeast surface display is a powerful technology for engineering proteins to improve their activity, specificity and stability as well as protein-protein interaction studies. WebCultivation profile of BJ5465.sfp.bpsA in different carbon sources. Concentrations of indigoidine (blue bars), consumed sugar (yellow line), dry cell weight (DCW, green line) and the by-products... can fisher cats swim
Production efficiency of the bacterial non-ribosomal peptide ...
WebTotal vector size (bp) 8218 Modifications to backbone yEVenus promoter replaced with minimal promoter and multiple cloning site. Vector type Yeast Expression, Synthetic Biology Selectable markers URA3 ; Nourseothricin … WebSaccharomyces cerevisiae strain BJ5465 was from LGC Promochem, whereas Escherichia coli XL1-Blue competent cells were from Stratagene. The expression shuttle vector pJRoC30, with uracil auxotrophy and an ampicillin marker for selection, came from the California Institute of Technology. ... DNA polymerase, and yeast transformation kit were ... WebJul 1, 2014 · All yeast strains used in this study are derivatives of BJ5465 (MATa ura3-52 trp1 leu2Δ1 his3Δ200 pep4::HIS3 prb1Δ1.6R can1). ... Yeast cells were grown at 30°C in SD medium to saturation, and sequential 10-fold serial dilutions were made. For temperature sensitivity test, the diluted samples were spotted onto YPD (1% yeast extract, 2% ... can fishers swim