L’homme souffrant en quête de sens: du récit de soi à l’identité narrative. Une réflexion à partir de Ricœur

The question of personal identity is central to any reflection on mankind and, therefore, immediately relevant to clinical anthropology. The notion of the continuity of personal identity over time represents Ric?ur’s contribution to the question. Upheaval and continuity in life are integrated into self-narrative, enabling temporal permanence of identity, which generates reflective consciousness and its concomitant ethical dimension. But from this anthropological point of view, the subject doesn’t construct a self and world through narrative. On the contrary, it is narrative elements that construct the subject, allowing the subject to make sense of his or her subjective life in the world. Through this narrative conception of the suffering individual, Ric?ur makes a distinct contribution to discourse in clinical anthropology in positing that suffering is a part of a person’s effort to recount their lives.     

The conjugating green alga Zygnema sp. (Zygnematophyceae) from the Arctic shows high frost tolerance in mature cells (pre-akinetes)

Protoplasma - Green algae of the genus Zygnema form extensive mats and produce large amounts of biomass in shallow freshwater habitats. Environmental stresses including freezing may perturb these...     

Chemical synthesis, cloning and expression in mammalian cells of a gene coding for human tissue-type plasminogen activator

A 1610-bp DNA duplex coding for human tissue-type plasminogen activator has been chemically synthesized using the phosphoramidite procedure, adapted for a custom-built gene synthesizer. The synthesizer, which was designed for both simplicity and speed, permits the rapid construction of relatively large genes and compares favorably in speed with alternative cDNA isolation procedures. The plasminogen activator gene has been expressed in mammalian cells and shown to produce authentic protein by an immuno-activity assay.     

Late breeding season definitive prebasic molt in males,and late breeding season brood care by females,in central California Wilson’s warblers

I made observations of a central California population of Wilson''s Warbler, Cardellina pusilla, after July 1 over 10 breeding seasons. I sighted males in definitive prebasic molt from July 4 (in 2007) to September 1 (in 1999). Most territorial males molted on their breeding territories, and individual molt lasted up to 46 days. Following prebasic molt, territorial males engaged in subdued “post‐molt singing,” which lasted about 7 days in some males, and which I first heard on August 13 (in 2004) and last heard on September 6 (in 1999). I sighted no female in definitive prebasic molt, or in fresh basic plumage, during the study. Of 13 females sighted ≥ July 21, 11 were in late breeding season uniparental brood care, and I could not rule out late brood care for the other two. Most, and possibly all, females not engaged in late season uniparental brood care apparently vacated their breeding territories before July 21. This departure was much earlier than for resident males, the last of which I sighted on September 10 (in 1999). Early‐departing females presumably underwent prebasic molt after July 21 at locations not known. Remaining late‐nesting females must have molted much later than resident males and likely later than early‐departing females, and at locations unknown. I last sighted two uniparental brood‐tending females, still in worn plumage, on August 26 and 29, respectively. Two unique findings of this study are a male/female difference in location of prebasic molt, and a likely dichotomy of prebasic molt timing between females leaving their breeding territories early and those remaining in uniparental brood care. Another finding, post‐molt singing in most and possible all territorial males, is a largely unrecognized behavior, but one previously reported in several passerine species. Post‐molt singing may reliably indicate completion of prebasic molt.     

The alpha-glucuronidase,GlcA67A,of Cellvibrio japonicus utilizes the carboxylate and methyl groups of aldobiouronic acid as important substrate recognition determinants

alpha-Glucuronidases are key components of the ensemble of enzymes that degrade the plant cell wall. They hydrolyze the alpha1,2-glycosidic bond between 4-O-methyl-d-glucuronic acid (4-O-MeGlcA) and the xylan or xylooligosaccharide backbone. Here we report the crystal structure of an inactive mutant (E292A) of the alpha-glucuronidase, GlcA67A, from Cellvibrio japonicus in complex with its substrate. The data show that the 4-O-methyl group of the substrate is accommodated within a hydrophobic sheath flanked by Val-210 and Trp-160, whereas the carboxylate moiety is located within a positively charged region of the substrate-binding pocket. The carboxylate side chains of Glu-393 and Asp-365, on the "beta-face" of 4-O-MeGlcA, form hydrogen bonds with a water molecule that is perfectly positioned to mount a nucleophilic attack at the anomeric carbon of the target glycosidic bond, providing further support for the view that, singly or together, these amino acids function as the catalytic base. The capacity of reaction products and product analogues to inhibit GlcA67A shows that the 4-O-methyl group, the carboxylate, and the xylose sugar of aldobiouronic acid all play an important role in substrate binding. Site-directed mutagenesis informed by the crystal structure of enzyme-ligand complexes was used to probe the importance of highly conserved residues at the active site of GlcA67A. The biochemical properties of K288A, R325A, and K360A show that a constellation of three basic amino acids (Lys-288, Arg-325, and Lys-360) plays a critical role in binding the carboxylate moiety of 4-O-MeGlcA. Disruption of the apolar nature of the pocket created by Val-210 (V210N and V210S) has a detrimental effect on substrate binding, although the reduction in affinity is not reflected by an inability to accommodate the 4-O-methyl group. Replacing the two tryptophan residues that stack against the sugar rings of the substrate with alanine (W160A and W543A) greatly reduced activity.     

Arthrobacter aurescens TC1 metabolizes diverse s-triazine ring compounds

Arthrobacter aurescens strain TC1 was isolated without enrichment by plating atrazine-contaminated soil directly onto atrazine-clearing plates. A. aurescens TC1 grew in liquid medium with atrazine as the sole source of nitrogen, carbon, and energy, consuming up to 3,000 mg of atrazine per liter. A. aurescens TC1 is metabolically diverse and grew on a wider range of s-triazine compounds than any bacterium previously characterized. The 23 s-triazine substrates serving as the sole nitrogen source included the herbicides ametryn, atratone, cyanazine, prometryn, and simazine. Moreover, atrazine substrate analogs containing fluorine, mercaptan, and cyano groups in place of the chlorine substituent were also growth substrates. Analogs containing hydrogen, azido, and amino functionalities in place of chlorine were not growth substrates. A. aurescens TC1 also metabolized compounds containing chlorine plus N-ethyl, N-propyl, N-butyl, N-s-butyl, N-isobutyl, or N-t-butyl substituents on the s-triazine ring. Atrazine was metabolized to alkylamines and cyanuric acid, the latter accumulating stoichiometrically. Ethylamine and isopropylamine each served as the source of carbon and nitrogen for growth. PCR experiments identified genes with high sequence identity to atzB and atzC, but not to atzA, from Pseudomonas sp. strain ADP.