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At the Metrology Light Source, a 630 MeV electron storage ring for the use of synchrotron radiation for metrology applications, a new beamline is dedicated to radiometry in the vacuum-ultraviolet spectral range. The emphasis lies on the traceability of measurements and profound uncertainty analysis. To replace the previously existing normal incidence monochromator beamline which serviced for more than 20 years now at different facilities, a newly designed 2 m off-plane Eagle monochromator beamline concept was developed. Different reflective coatings for mirrors and gratings in combination with order-sorting filters ensure highest spectral purity of the monochromatized radiation in combination with optimized photon flux characteristics. The beamline is planned to go into full operation in late 2022.

Efficient polarizing as well as non-polarizing mirrors for a wavelength of λ =121.6 nm (hydrogen Lyman- α radiation) are necessary to achieve an experimental determination of the magnetic field in the solar corona through the Hanle effect. We have designed, realized and characterized such mirrors. These consist of glass coated with a thin-film stack. The coatings use the most reflective (Al) and most transparent (fluorides) materials at this wavelength. Different coatings were explored which involve an increasing number of films in the coating stack. At the incident angle of maximum polarization where the p-polarized reflectivity R p is minimized, an s-polarized reflectivity R s as high as 69% is experimentally obtained with a coating made of a Fabry–Pérot resonator. To our knowledge, this value is the highest ever reported for a polarizing mirror at this wavelength. Additionally, efficient non-polarizing mirrors have been designed and realized by using a two-layer coating (MgF 2 /Al/glass). By optimizing the fluoride layer thickness, a mirror with non-polarizing properties in the whole range of incident angles was realized.

We present a long-term assessment of the radiometric calibration and degradation of the Large Yield Radiometer (LYRA), which has been on orbit since 2009. LYRA is an ultraviolet (UV) solar radiometer and is the first space experiment using aboard a pioneering diamond detector technology. We show that LYRA has degraded after the commissioning phase but is still exploitable scientifically after almost 5 years on orbit thanks to its redundancy design and calibration strategy correcting for instrument degradation. We focus on the inflight detector’s calibration and show that diamond photodetectors have not degraded while silicon reference photodiodes that are even less exposed to the Sun show an increase of their dark current and a decrease of their photoresponse.

Fabrication, packaging and experimental results on the calibration of metal-semiconductor-metal (MSM) photodetectors made on diamond are reported. LYRA (Lyman-α RAdiometer onboard PROBA-2) will use diamond detectors for the first time in space for a solar physics instrument. A set of measurement campaigns was designed to obtain the XUV-to-VIS responsivity of the devices and other characterizations. The measurements of responsivity in EUV and VUV spectral ranges (40–240 nm) have been carried out by the Physkalisch-Technische Bundesanstalt (PTB) in Germany at the electron storage ring BESSY II. The longer wavelength range from 210 to 1127 nm was measured with monochromatic light by using a Xe-lamp at IMO-IMOMEC. The diamond detectors exhibit a photoresponse which lie in the 35–65 mA/W range at 200 nm (corresponding to an external quantum efficiency of 20–40%) and indicate a visible rejection ratio (200–500 nm) higher than four orders of magnitude.

In contrast to 16:3 plants like rapeseed (Brassica napus), which contain alpha-linolenic acid (18:3(Delta9,12,15)) and hexadecatrienoic acid (16:3(Delta7,10,13)) as major polyunsaturated fatty acids in leaves, the silica-less diatom Phaeodactylum tricornutum contains eicosapentaenoic acid (EPA; 20:5(Delta5,8,11,14,17)) and a different isomer of hexadecatrienoic acid (16:3(Delta6,9,12)). In this report, we describe the characterization of two cDNAs having sequence homology to Delta12-fatty acid desaturases from higher plants. These cDNAs were shown to code for a microsomal and a plastidial Delta12-desaturase (PtFAD2 and PtFAD6, respectively) by heterologous expression in yeast (Saccharomyces cerevisiae) and Synechococcus, respectively. Using these systems in the presence of exogenously supplied fatty acids, the substrate specificities of the two desaturases were determined and compared with those of the corresponding rapeseed enzymes (BnFAD2 and BnFAD6). The microsomal desaturases were similarly specific for oleic acid (18:1(Delta9)), suggesting that PtFAD2 is involved in the biosynthesis of EPA. In contrast, the plastidial desaturase from the higher plant and the diatom clearly differed. Although the rapeseed plastidial desaturase showed high activity toward the omega9-fatty acids 18:1(Delta9) and 16:1(Delta7), in line with the fatty acid composition of rapeseed leaves, the enzyme of P. tricornutum was highly specific for 16:1(Delta9). Our results indicate that in contrast to EPA, which is synthesized in the microsomes, the hexadecatrienoic acid isomer found in P. tricornutum (16:3(Delta6,9,12)) is of plastidial origin.

The THEMIS Fluxgate Magnetometer (FGM) measures the background magnetic field and its low frequency fluctuations (up to 64 Hz) in the near-Earth space. The FGM is capable of detecting variations of the magnetic field with amplitudes of 0.01 nT, and it is particularly designed to study abrupt reconfigurations of the Earth’s magnetosphere during the substorm onset phase. The FGM uses an updated technology developed in Germany that digitizes the sensor signals directly and replaces the analog hardware by software. Use of the digital fluxgate technology results in lower mass of the instrument and improved robustness. The present paper gives a description of the FGM experimental design and the data products, the extended calibration tests made before spacecraft launch, and first results of its magnetic field measurements during the first half year in space. It is also shown that the FGM on board the five THEMIS spacecraft well meets and even exceeds the required conditions of the stability and the resolution for the magnetometer.

Plastids of diatoms and related algae evolved by secondary endocytobiosis, the uptake of a eukaryotic alga into a eukaryotic host cell and its subsequent reduction into an organelle. As a result diatom plastids are surrounded by four membranes. Protein targeting of nucleus encoded plastid proteins across these membranes depends on N-terminal bipartite presequences consisting of a signal and a transit peptide-like domain. Diatoms and cryptophytes share a conserved amino acid motif of unknown function at the cleavage site of the signal peptides (ASAFAP), which is particularly important for successful plastid targeting. Screening genomic databases we found that in rare cases the very conserved phenylalanine within the motif may be replaced by tryptophan, tyrosine or leucine. To test such unusual presequences for functionality and to better understand the role of the motif and putative receptor proteins involved in targeting, we constructed presequence:GFP fusion proteins with or without modifications of the “ASAFAP”-motif and expressed them in the diatom Phaeodactylum tricornutum. In this comprehensive mutational analysis we found that only the aromatic amino acids phenylalanine, tryptophan, tyrosine and the bulky amino acid leucine at the +1 position of the predicted signal peptidase cleavage site allow plastid import, as expected from the sequence comparison of native plastid targeting presequences of P. tricornutum and the cryptophyte Guillardia theta. Deletions within the signal peptide domains also impaired plastid import, showing that the presence of F at the N-terminus of the transit peptide together with a cleavable signal peptide is crucial for plastid import.

The complex plastid of the cryptophyte Guillardia theta and of the diatom Phaeodactylum tricornutum can both be traced back to an engulfed eukaryotic red alga. The eukaryotic origin of these plastids is most obvious in cryptophytes, where the organelle still possesses a remnant nucleus, the nucleomorph. The nucleomorph itself is embedded in the periplastid compartment (PPC), the remnant of the former red algal cytosol. In the cryptophyte and diatom, the complex plastid is surrounded by 4 membranes, the outer one being continuous with the host rough endoplasmatic reticulum. In a recent report, we have shown that a nuclear encoded PPC protein of G. theta expressed in P. tricornutum leads to a localization, recently described as being a “bloblike structure,” which can be obtained by mutation of plastid protein–targeting sequences of the diatom itself.Here we present further nucleus-encoded PPC proteins from G. theta, such as the eukaryotic translation elongation factor-1α, evidence for their nucleus-to-nucleus gene transfer, and retargeting of the proteins. We also investigated the first nuclear encoded PPC-targeted protein of P. tricornutum (Hsp70) and analyzed it for in vivo localization together with the identified G. theta PPC proteins. This revealed that all localize to the bloblike structures, which we suggest is the highly reduced PPC of P. tricornutum. Furthermore, the described cryptophyte PPC proteins possibly allow the elucidation of the processes by which proteins are involved in different levels of host control over its eukaryotic organelle.

In contrast to 16:3 plants like rapeseed (Brassica napus), which contain alpha -linolenic acid (18:3 super( Delta 9,12,15)) and hexadecatrienoic acid (16:3 super( Delta 7,10,13)) as major polyunsaturated fatty acids in leaves, the silica-less diatom Phaeodactylum tricornutum contains eicosapentaenoic acid (EPA; 20:5 super( Delta 5,8,11,14,17)) and a different isomer of hexadecatrienoic acid (16:3 super( Delta 6,9,12)). In this report, we describe the characterization of two cDNAs having sequence homology to Delta 12-fatty acid desaturases from higher plants. These cDNAs were shown to code for a microsomal and a plastidial Delta 12-desaturase (PtFAD2 and PtFAD6, respectively) by heterologous expression in yeast (Saccharomyces cerevisiae) and Synechococcus, respectively. Using these systems in the presence of exogenously supplied fatty acids, the substrate specificities of the two desaturases were determined and compared with those of the corresponding rapeseed enzymes (BnFAD2 and BnFAD6). The microsomal desaturases were similarly specific for oleic acid (18:1 super( Delta 9)), suggesting that PtFAD2 is involved in the biosynthesis of EPA. In contrast, the plastidial desaturase from the higher plant and the diatom clearly differed. Although the rapeseed plastidial desaturase showed high activity toward the omega 9-fatty acids 18:1 super( Delta 9) and 16:1 super( Delta 7), in line with the fatty acid composition of rapeseed leaves, the enzyme of P. tricornutum was highly specific for 16:1 super( Delta 9). Our results indicate that in contrast to EPA, which is synthesized in the microsomes, the hexadecatrienoic acid isomer found in P. tricornutum (16:3 super( Delta 6,9,12)) is of plastidial origin.

Soft tissue complications are clinically relevant problems after osteosynthesis of fractures. The goal is to develop a method for reduction of fibroblast adhesion and proliferation on titanium implant surfaces by plasma polymerisation of the organo-silicon monomer hexamethyldisiloxane (HMDSO). HMDSO was deposited under continuous wave conditions in excess oxygen (ppHMDSO surface) and selected samples were further modified with an additional oxygen plasma (ppHMDSO + O 2 surface). Surface characterization was performed by scanning electron microscopy, profilometry, water contact angle measurements, infrared reflection absorption spectroscopy and X-ray photoelectron spectroscopy. In our experimental setup the mechanical properties, roughness and topography of the titanium were preserved, while surface chemistry was drastically changed. Fibroblast proliferation was assessed by alamarBlue assay, cell morphology by confocal microscopy visualization of eGFP-transducted fibroblasts, and cell viability by Annexine V/propidium iodide assay. Both modified surfaces, non-activated hydrophobic ppHMDSO and activated hydrophilic ppHMDSO + O 2 were able to dramatically reduce fibroblast colonization and proliferation compared to standard titanium. However, this effect was more strongly pronounced on the hydrophobic ppHMDSO surface, which caused reduced cell adhesion and prevented proliferation of fibroblasts. The results demonstrate that plasma modifications of titanium using HMDSO are valuable candidates for future developments in anti-adhesive and anti-proliferative coatings for titanium fracture implants.