ABSTRACT
Coprinoferrin (CPF), originally isolated from a genetically engineered strain (ΔlaeA) of the mushroom fungus Coprinopsis cinerea, is an acylated tripeptide hydroxamate consisting of tandem aligned N5-hexanoyl-N5-hydroxy-L-ornithine with modifications of N-acetyl and C-carboxamide. These unique chemical properties make CPF an iron(III) binder (siderophore), which helps in iron acquisition from the environment and promotes hyphal growth as well as fruiting body formation in C. cinerea. However, CPF's detailed mode of action remains enigmatic. In this study, we have accomplished the synthesis of CPF from N-Boc-L-glutamic acid 5-benzyl ester. The physicochemical characteristics, spectroscopic features, and biological activity observed in the synthetic CPF closely match those of natural CPF. This alignment provides unequivocal confirmation of the proposed chemical structure, facilitating a deeper understanding of its physiological role in nature, particularly in fruiting body formation.
Subject(s)
Ferric Compounds , Siderophores , Siderophores/chemistry , Iron , Hydroxamic Acids/pharmacologyABSTRACT
Quantum vacuum fluctuations impose strict limits on precision displacement measurements, those of interferometric gravitational-wave detectors among them. Introducing squeezed states into an interferometer's readout port can improve the sensitivity of the instrument, leading to richer astrophysical observations. However, optomechanical interactions dictate that the vacuum's squeezed quadrature must rotate by 90° around 50 Hz. Here we use a 2-m-long, high-finesse optical resonator to produce frequency-dependent rotation around 1.2 kHz. This demonstration of audio-band frequency-dependent squeezing uses technology and methods that are scalable to the required rotation frequency and validates previously developed theoretical models, heralding application of the technique in future gravitational-wave detectors.