The spin-coherent quantum transport through multiwall carbon nanotubes contacted by ferromagnetic Co pads is investigated experimentally. At 4.2 K, the devices show a remarkable increase of the magnetoresistance (MR) ratio with decreasing junction bias, reaching a maximum MR ratio of 30% at a junction bias current of 1 nA. The experimental results suggest the transport to be dominated by spin-dependent tunneling processes at the Co/nanotube interfaces and governed by the local magnetization. We also observe an asymmetry of the magnetoresistance peak position and width which is attributed to a local exchange biasing in the electrode material.

SUMMARY The adenylation (A) domains of nonribosomal peptide synthetases (NRPSs) activate aryl acids or amino acids to launch their transfer through the NRPS assembly line for the biosynthesis of many medicinally important natural products. In order to expand the substrate pool of NRPSs, we developed a method based on yeast cell surface display to engineer the substrate specificities of the A-domains. We acquired A-domain mutants of DhbE that have 11- and 6-fold increases in kcat/Km with nonnative substrates 3-hydroxybenzoic acid and 2-aminobenzoic acid, respectively and corresponding 3- and 33-fold decreases in kcat/Km values with the native substrate 2,3-dihydroxybenzoic acid, resulting in a dramatic switch in substrate specificity of up to 200-fold. Our study demonstrates that yeast display can be used as a high throughput selection platform to reprogram the “nonribosomal code” of A-domains.

Engineering the ubiquitin transfer cascades by phage display enables an efficient way to profile E3 substrates.

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