Structure and spectroscopy of methionyl-methionine for aquaculture

The amino acid L-methionine is an essential amino acid and is commonly used as a feed supplement in terrestrial animals. It is less suitable for marine organisms because it is readily excreted. It is also highly water soluble and this results in loss of the feed and eutrophication of the water. To address these problems, the dipeptide DL-methionyl-DL-methionine (trade name: AQUAVI Met-Met) has been developed as a dedicated methionine source for aquaculture. The commercial product is a mixture of a racemic crystal form of D-methionyl-D-methionine/L-methionyl-L-methionine and a racemic crystal form of D-methionyl-L-methionine/L-methionyl-D-methionine. In this work, we have computationally, structurally, spectroscopically and by electron microscopy characterised these materials. The microscopy and spectroscopy demonstrate that there is no interaction between the DD–LL and DL–LD racemates on any length scale from the macroscopic to the nanoscal

Towards a Pattern Recognition Approach for Transferring Knowledge in ACM

In Adaptive Case Management (ACM) systems, knowledge workers have the flexibility to deal with unpredictable situations. Compared with a classical BPM approach the extensive prescriptive process analysis and definitions are replaced by context-sensitive proposals, which is more suited for knowledge-intensive work. Thus, it is vital that ACM systems support knowledge workers with knowledge captured from previous work which can be ambiguous for the system. This paper proposes an approach to support knowledge workers based on the knowledge previously applied by others in the form of a User Trained Agent that learns from ad hoc actions taken by knowledge workers to suggest best next actions for the current situation. The proposed best next actions are analyzed for coherence.Interne Organisation & Information Servic

Fatigue Behavior of Ultrafine-Grained Medium Carbon Steel with Different Carbide Morphologies Processed by High Pressure Torsion

The increased attention ultrafine grained (UFG) materials have received over the last decade has been inspired by their high strength in combination with a remarkable ductility, which is a promising combination for good fatigue properties. In this paper, we focus on the effect of different carbide morphologies in the initial microstructure on the fatigue behavior after high pressure torsion (HPT) treatment of SAE 1045 steels. The two initial carbide morphologies are spheroidized as well as tempered states. The HPT processing increased the hardness of the spheroidized and tempered states from 169 HV and 388 HV to a maximum of 511 HV and 758 HV, respectively. The endurance limit increased linearly with hardness up to about 500 HV independent of the carbide morphology. The fracture surfaces revealed mostly flat fatigue fracture surfaces with crack initiation at the surface or, more often, at non-metallic inclusions. Morphology and crack initiation mechanisms were changed by the severe plastic deformation. The residual fracture surface of specimens with spheroidal initial microstructures showed well-defined dimple structures also after HPT at high fatigue limits and high hardness values. In contrast, the specimens with a tempered initial microstructure showed rather brittle and rough residual fracture surfaces after HPT

Centrosome-dependent microtubule modifications set the conditions for axon formation

Microtubule (MT) modifications are critical during axon development, with stable MTs populating the axon. How these modifications are spatially coordinated is unclear. Here, via high-resolution microscopy, we show that early developing neurons have fewer somatic acetylated MTs restricted near the centrosome. At later stages, however, acetylated MTs spread out in soma and concentrate in growing axon. Live imaging in early plated neurons of the MT plus-end protein, EB3, show increased displacement and growth rate near the MTOC, suggesting local differences that might support axon selection. Moreover, F-actin disruption in early developing neurons, which show fewer somatic acetylated MTs, does not induce multiple axons, unlike later stages. Overexpression of centrosomal protein 120 (Cep120), which promotes MT acetylation/stabilization, induces multiple axons, while its knockdown downregulates proteins modulating MT dynamics and stability, hampering axon formation. Collectively, we show how centrosome-dependent MT modifications contribute to axon formation