Activation and detoxification of cassava cyanogenic glucosides by the whitefly Bemisia tabaci.

Two-component plant defenses such as cyanogenic glucosides are produced by many plant species, but phloem-feeding herbivores have long been thought not to activate these defenses due to their mode of feeding, which causes only minimal tissue damage. Here, however, we report that cyanogenic glycoside defenses from cassava (Manihot esculenta), a major staple crop in Africa, are activated during feeding by a pest insect, the whitefly Bemisia tabaci, and the resulting hydrogen cyanide is detoxified by conversion to beta-cyanoalanine. Additionally, B. tabaci was found to utilize two metabolic mechanisms to detoxify cyanogenic glucosides by conversion to non-activatable derivatives. First, the cyanogenic glycoside linamarin was glucosylated 1-4 times in succession in a reaction catalyzed by two B. tabaci glycoside hydrolase family 13 enzymes in vitro utilizing sucrose as a co-substrate. Second, both linamarin and the glucosylated linamarin derivatives were phosphorylated. Both phosphorylation and glucosidation of linamarin render this plant pro-toxin inert to the activating plant enzyme linamarase, and thus these metabolic transformations can be considered pre-emptive detoxification strategies to avoid cyanogenesis.

Determination of K869, a Novel Oxime Reactivator of Acetylcholinesterase, in Rat Body Fluids and Tissues by Liquid-Chromatography Methods: Pharmacokinetic Study.

Oxime reactivators of acetylcholinesterase (AChE) represent an integral part of standard antidote treatment of organophosphate poisoning. Oxime K869 is a novel bisquaternary non-symmetric pyridinium aldoxime with two pyridinium rings connected by a tetramethylene bridge where two chlorines modify the pyridinium ring bearing the oxime moiety. Based on in vitro assays, K869 is a potent AChE and butyrylcholinesterase (BChE) reactivator. For the investigation of the basic pharmacokinetic properties of K869 after its intramuscular application, new HPLC-UV and LC-MS/MS methods were developed and validated for its determination in rat body fluids and tissues. In this study, the SPE procedure for sample pretreatment was optimized as an alternative to routine protein precipitation widely used in oxime pharmacokinetics studies. K869 oxime is quickly absorbed into the central compartment reaching its maximum in plasma (39 ± 4 µg/mL) between 15 and 20 min. The majority of K869 was eliminated by kidneys via urine when compared with biliary excretion. However, only a limited amount of K869 (65 ± 4 ng/g of brain tissue) was found in the brain 30 min after oxime administration. Regarding the brain/plasma ratio calculated (less than 1%), the penetration of K869 into the brain did not exceed conventionally used oximes.

Microstructural Investigation of LME Crack Initiated in Ferritic/Martensitic Steel T91 Loaded in Liquid Lead-Bismuth Eutectic at 300 °C.

Liquid lead-bismuth eutectic (LBE) is one of the candidate materials for advanced nuclear systems. The structural materials used in contact with LBE are selected according to the resistance to liquid metal corrosion, irradiation embrittlement, and compatibility with the coolant. However, simultaneous presence of mechanical strain and LBE environment can induce liquid metal embrittlement (LME) in these materials. In this study, a specimen from candidate ferritic-martensitic steel T91 was tested by Constant Extension Rate Tensile (CERT) test exposed to PbBi environment with oxygen concentration 6 × 10-6 wt % at 300 °C up to rupture. Post-test examination using scanning electron microscopy (SEM) showed a deep crack indicating features of LME in the plastic strained region of the tested specimen. Further investigations focused on characterization of the fracture path and microstructure determination using focused ion beam (FIB) and energy dispersive X-ray spectrometry/electron backscatter diffraction (EDX/EBSD). This observation revealed that the dominant LME failure mode of the observed crack is translath or transgranular and the crack stopped at the high-angle grain boundary. The role of oxides in the crack initiation is discussed.

Effect of Applied Stress on T91 Steel Performance in Liquid Lead at 400 °C.

The environmental performance of structural materials (e.g., corrosion and environmental assisted cracking) is one of the critical issues being addressed in the development of Generation IV fast reactors. This work aims to support the study of the performance of the ferritic-martensitic steel T91 in liquid lead, under close to operation conditions, in order to assess its suitability for an application in lead fast reactors. T91 steel was tested in air and liquid lead at 400 °C using static and slow loading regimes. Applied stresses were chosen to be slightly above the yield strength in order to evaluate the threshold stress and strain for crack initiation. Three-point bending static exposure and constant extension tests of tapered specimens were performed. Post-test surfaces and cross sections of specimens were observed using scanning electron microscopy techniques in order to detect cracks and to analyze oxide layers. The effect of strain rate of the oxide layer cracking was observed. In conclusion, T91 was not susceptible to liquid metal embrittlement, a special case of environmentally assisted cracking under the testing conditions. The cracking conditions are discussed based on previous experience.