We demonstrate the generation of extreme-ultraviolet (XUV) free-electron laser (FEL) pulses with time-dependent polarization. To achieve polarization modulation on a femtosecond timescale, we combine two mutually delayed counterrotating circularly polarized subpulses from two cross-polarized undulators. The polarization profile of the pulses is probed by angle-resolved photoemission and above-threshold ionization of helium; the results agree with solutions of the time-dependent Schrödinger equation.
View Article and Find Full Text PDFTriggering and switching magnetic moments is of key importance for applications ranging from spintronics to quantum information. A noninvasive ultrafast control at the nanoscale is, however, an open challenge. Here, we propose a novel laser-based scheme for generating atomic-scale charge current loops within femtoseconds.
View Article and Find Full Text PDFBacterial natural products in general, and non-ribosomally synthesized peptides in particular, are structurally diverse and provide us with a broad range of pharmaceutically relevant bioactivities. Yet, traditional natural product research suffers from rediscovering the same scaffolds and has been stigmatized as inefficient, time-, labour- and cost-intensive. Combinatorial chemistry, on the other hand, can produce new molecules in greater numbers, cheaper and in less time than traditional natural product discovery, but also fails to meet current medical needs due to the limited biologically relevant chemical space that can be addressed.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2021
Non-ribosomal peptide synthetases (NRPSs) are the origin of a wide range of natural products, including many clinically used drugs. Efficient engineering of these often giant biosynthetic machineries to produce novel non-ribosomal peptides (NRPs) is an ongoing challenge. Here we describe a cloning and co-expression strategy to functionally combine NRPS fragments of Gram-negative and -positive origin, synthesising novel peptides at titres up to 220 mg L .
View Article and Find Full Text PDFNon-ribosomal peptide synthetases (NRPS) produce natural products from amino acid building blocks. They often consist of multiple polypeptide chains which assemble in a specific linear order via specialized N- and C-terminal docking domains ( DDs). Typically, docking domains function independently from other domains in NRPS assembly.
View Article and Find Full Text PDFWe study theoretically the transfer of the light field orbital angular momentum (OAM) to propagating electrons upon photoemission from quantum well states. Irradiation with a Laguerre-Gaussian mode laser pulse elevates the quantum well state into a laser-dressed Volkov state that can be detected in an angular and energy-resolved manner while varying the characteristics of the driving fields. We derive the photoemission cross section for this process using the S-matrix theory and illustrate how the OAM is embodied in the photoelectron angular pattern with the aid of numerical calculations.
View Article and Find Full Text PDFWe study theoretically the electron quantum dynamics in atoms driven by intense IR laser pulses that are phase and/or polarization structured. The extremely non-linear electron dynamics causes high harmonic emission, which we calculate, analyze, and characterize. Results are presented for three different types of structured lasers: radially polarized and azimuthally polarized beams and optical skyrmions.
View Article and Find Full Text PDFNonribosomal peptide synthetases (NRPSs) produce a wide variety of different natural products from amino acid precursors. In contrast to single protein NRPS, the NRPS of the bacterium producing the peptide-antimicrobial-Xenorhabdus (PAX) peptide consists of three individual proteins (PaxA/B/C), which interact with each other noncovalently in a linear fashion. The specific interactions between the three different proteins in this NRPS system are mediated by short C- and N-terminal docking domains (DDs).
View Article and Find Full Text PDFA single-atom "double-slit" experiment is realized by photoionizing rubidium atoms using two independent low power lasers. The photoelectron wave of well-defined energy recedes to the continuum either from the 5P or 6P states in the same atom, resulting in two-path interference imaged in the far field using a photoelectron detector. Even though the lasers are independent and not phase locked, the transitions within the atom impart the phase relationship necessary for interference.
View Article and Find Full Text PDFSpin Hall effect, one of the cornerstones in spintronics refers to the emergence of an imbalance in the spin density transverse to a charge flow in a sample under voltage bias. This study points to a novel way for an ultrafast generation and tuning of a unidirectional nonlinear spin Hall current by means of subpicosecond laser pulses of optical vortices. When interacting with matter, the optical orbital angular momentum (OAM) carried by the vortex and quantified by its topological charge is transferred to the charge carriers.
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