64,275 research outputs found
Juris naturae, et gentium principia, et officia ad christianae doctrinae regulam exacta, et explicata a doctore eximio Francisco Suarez ... Digessit, notisque perpetuis illustravit Joannes Baptista Guarini ...
Panormi : ex typographia Francisci Ferrer, sub signo S. Calcidonii m., 1758
Fregi e iniziali xil
Segn.: [pigreco]2 A-L8 M4
Errata a c. M4r.
Legato con altre opere. Legatura in pergamena rigida
https://galileodiscovery.unipd.it/discovery/fulldisplay?context=L&vid=39UPD_INST:VU1&search_scope=MyInst_and_CI&tab=Everything&docid=alma99002631114020604
Tentyria bifida Bujalance, Cardenas, Ferrer & Gallardo 2016
<i>Tentyria bifida</i> Bujalance, Cárdenas, Ferrer & Gallardo, 2016 (Figs. 35, 69, 105, 140, 153, 185, 221) <p> <i>Tentyria bifida</i> Bujalance, Cárdenas, Ferrer & Gallardo, 2016: 350; Martínez 2018: 58, Iwan & L̂bl 2020: 248.</p> <p> <b>Types examined</b>: Holotype ♁: Caño Mayor, Doñana N. P. (Huelva); 28.VII.2005, J.L. Bujalance leg. (MNCN). Paratypes: same data as the Holotype (11♁♁ and 21♀♀, CJLB) (1♁ and 1♀, CACT) (1♀, CJF). Caño Mayor, Doñana N. P., 6.VII.2005, J.L. Bujalance leg. (5♁♁ and 3♀♀, CJLB) (2♁♁ and 1♀, CJF); El Charco de la Boca, Doñana N. P., 25.XI.2001, A. Cárdenas leg. (1♀, CUCO); 7.VIII.2001 (1 ex, CUCO); 30.VII.2001 (1♁ and 3♀♀, CUCO). La Casa de la Pichiricha, Doñana N. P., 25.VI.2001 (3♁♁ and 1♀, CUCO); 16.VII.2001 (1♀, CUCO); 30.VII.2001 (17♁♁ and 23♀♀, CUCO); 6.VII.2001 (1♀, CUCO); 7.VIII.2001 (3♁♁ and 3♀♀, CUCO); 25.IX.2001 (2 exx, CUCO). Matasgordas, Doñana N. P., 30.VII.2001 (5♁♁, 1♀, and 1 specimen, CUCO).</p> <p> <b>Diagnosis</b>: Body somewhat elongated (Fig. 221); smooth, black intense and bright tegument, particularly in the ventral side. Head (Fig. 35) shaped as in <i>Tentyria platyceps</i> Steven, subtriangular epistome slightly protruding forward, provided with a tooth at the middle; punctures quite fine but perceptible, not confluent and greater that in the pronotum; sub-right and transverse, well defined, broad and deep gular groove (Fig. 69), but not as deep than in <i>T. platyceps</i>; pronotum (Fig. 105) moderately transverse and convex, sided curved and narrowed towards the base, barely rounded and prolonged backward; posterior angles obtuse but discernible, punctures very fine and sparse; prosternal apophysis (Fig. 140) long and narrow, with the extreme bent upward in ventral view and surpassing backwards the level of procoxae. Protibiae not showing sexual dimorphism, with the margin right and progressively widened to the apex; elytra convex, smooth, punctures very fine, even more that in the pronotum, ovate and elongate, and almost as narrowed at the base as at the apex. Abdominal sternites smooth and bright, last urosternite with the apex bifid (Fig. 153). The aedeagus (Fig. 185) is small, with the parameres slightly strangled at the base and very curved in lateral view, conspicuously shorter and more curved than the phallobase.</p> <p> <b>Geographic distribution:</b> Endemism from Doñana National Park (Huelva) (Bujalance <i>et al.</i> 2016).</p>Published as part of <i>Bujalance, José L., Ferrer, Julio & Cárdenas, Ana M., 2023, A taxonomic revision of the genus Tentyria Latreille, 1802 in the Iberian Peninsula and Balearic Islands (Coleoptera: Tenebrionidae), pp. 1-88 in Zootaxa 5320 (1)</i> on pages 55-56, DOI: 10.11646/zootaxa.5320.1.1, <a href="http://zenodo.org/record/8203747">http://zenodo.org/record/8203747</a>
Tentyria donanensis Bujalance, Cardenas, Ferrer & Gallardo 2016
<i>Tentyria donanensis</i> Bujalance, Cárdenas, Ferrer & Gallardo, 2016 (Figs. 26, 60, 95, 96, 131, 178, 212) <p> <i>Tentyria donanensis</i> Bujalance, Cárdenas, Ferrer & Gallardo, 2016: 351; Martínez 2018: 58, Iwan & L̂bl 2020: 249.</p> <p> <i>Tentyria (Subtentyrina) gaditana</i> Rosenhauer Grimm & Aistleitner 2009: 70</p> <p> <b>Types examined</b>: Doñana Nacional Park (Huelva): Holotype, 15.III.2000, La Mancha Grande, A.M. Cárdenas leg. (♁, CJLB); Paratypes: Cruz de Dominguez, 15.III.2000, 24.VII.2000, A.M. Cárdenas leg. (20♁♁ and 32♀♀, CUCO); Palacio Doñana, 24.VII.2000, idem (4 exx, CUCO); Laguna del Taraje, 24.III.2000, idem (1♁, CJLB); 25.IX.2001, idem (1♀, CJF); El Puntal, 25.IX.2001, idem (3 exx, CUCO); La Cancela, 23.05.2000, idem (7 exx, CUCO); Cerro de los Ánsares, 7.VIII.2000, idem (43 exx, CUCO); Corral de la Liebre, 15.III.2000, idem (1♁, CJLB); Corral de la Liebre, 15.III.2000, idem (1♁ and 1♀, CJLB); La Vera, 28.V.2005, J.L. Bujalance leg. (2♁♁, CJLB and CJF); Nave del Inglesillo, 15.III.2000, A.M. Cárdenas leg. (1♀, CJLB); Pinar de San Agustín, 30.VII.2001, idem (1♁, CJLB); 25.IX.2001, idem (1♁ and 1♀, CJLB); idem, 01.IV.2005, J.L. Bujalance leg. (2♀♀, CJLB); El Nido del Gato, 21.II.2001, A.M. Cárdenas leg. (1♀, CJLB); idem, 27.VII.2005, J.L. Bujalance leg. (1♀, CJLB); La Mogea, 26.IX.2001, A.M. Cárdenas leg. (1♁, CJLB); idem, 30.X.2001, idem (1♀, CJLB); Casa de Manecorro, 26.IX.2001, idem (1♀, CJLB); idem, 25.IX.2001, idem (15 exx, CJF); El Charco de la Boca, 26.IV.2001, idem (2♀♀, CJLB); idem, 23.V.2001, idem (2♀♀, CJLB); Arroyo de la Rocina, 15.IX.2001, idem (1♁, CJF); Caño Mayor, 2.IV.2005, M. Baena leg. (3 exx, CACT); idem, 28.VII.2005, J.L. Bujalance leg. (1♀, CJLB); Sanlucar, 30.IV.2001, idem (1♀, CJLB).</p> <p> <b>Additional material</b>: <b>Huelva</b>: Matalascañas, 5.IV.2010, A. Castro Tovar leg. (4 exx, CACT); Matalascañas, Huelva 5.IV.2010 (1 ex, CACT); P. N. de Doñana, Caño Mayor / 2.IV.2005, M. Baena leg. (1 ex, CACT); P. natural Marismas del Odiel, Isla de Saltés / 11.VIII.2007 / J.J. López Pérez leg. (1♁ and 1♀, CACT); Guadalquivir, Espagne, 20.III.66, Coll. P. BONNEAU (1♀, CJF); Hispania Mer., Huelva, 1.IV.1999 / El Abalario, Bastazo and Vela leg. (2♁ and 1♀, CB&V); Huelva, Martinez! (1 ex, MNCN); Palma del Condado 22.VI.1981, B. Lassalle leg. (1 ex, CJF); Cartaya, 2.V.1996, J. Casas lg. (1 ex, CJGC); El Vigía, Playa, Palos de la Frontera, 1.IV.2006, JJ López-Pérez leg. (2♁, CJJLP); Moguer, Mazagón, playa, 10.IV.2006, JPG de la Vega leg. (2♁♁, CJJLP); Ayamonte, 8.IX.2006, JJ López-Pérez leg. (1♀, CJJLP); El Almendral, Isla Saltés, Huelva, 8.IV.2006, JJ López-Pérez leg. (1♁, CJJLP); Idem, 2.I.2007, JJ López-Pérez leg. (1♁ and 1♀, CJJLP); Idem, 12.III.2006, JJ López-Pérez leg. (2♀, CJJLP); Laguna de El Manto, Isla Saltés, Huelva, 18.III.2006, JJ López-Pérez leg. (1♁, CJJLP); La Cascajera, Isla Saltés, Huelva, 18.III.2006, JJ López-Pérez leg. (1♁ and 4♀♀, CJJLP); El Acebuchal, Isla Saltés, Huelva, 13.IV.2006, JJ López-Pérez leg. (2♁♁, CJJLP); Puerto Maltés, Punta Umbría, Huelva, 1.VI.2000, JJG. De la Vega leg. (1♀, CJJLP); Laguna 1ª de Palos, Palos de la Frontera, Huelva, 28.III.2007, JJ López-Pérez leg. (1♀, CJJLP).</p> <p> <b>Diagnosis:</b> Long body (Fig. 212), about 14.25 mm long on average, tegument smooth and shiny, mostly ventrally. Head short and rounded (Fig. 26), eyes very slightly convex, supraorbital folds parallel and slightly raised, epistome in continuous curve from the gena, showing a minute tooth in the middle; fine but clearly perceptible punctures; gular groove (Fig. 60) usually narrow and not well defined, often consisting only of a shallow central hollow. Pronotum (Figs. 95, 96) proportionately large and not very transverse, with sides in open curve and tapering equally towards both ends, the base finely bordered, in prolonged curve backwards and somewhat sinuate before the posterior angles which are very obtuse and hardly visible dorsally, especially in females; punctures fine and rather dense, more widely spaced on the disc; prosternal apophysis (Fig. 131) broad, parallel-sided, rounded at the end and not exceeding the procoxae. Elytra (Fig. 212) convex, moderately oval-elongated, with maximum width in the middle or frequently behind it, narrowed posteriorly in a straight line to the apex, which is very acute and surpasses the last abdominal sternite, by prolongation of the upper ridge of each epipleura which is more elongate than the lower; elytral ribs slightly indicated, punctures very fine and widely spaced; humeral angles very marked and the base notched in an arc. Aedeagus (Fig. 178) about 3.4 mm long on average, with the phallobase longer than the parameres, the latter tapering towards the apex in an almost straight, not sinuous, line.</p> <p> <b>Comments:</b> Geographically and morphologically this species is close to <i>T. gaditana</i> Rosenhauer from which it differs in the elytra which are ovate, elongated and sharpened at the apex, with signs of striae and finely punctured, more narrowed towards the base and the apex, of nonparallel sides; the humeri are more angulous, with the base narrower and cut in arc. The pronotum is as bright as the elytra, less densely but more finely punctured than in <i>T. gaditana</i>, less transverse, subcordiform, the base curved and clearly prolonged backwards, with the posterior angles very obtuse and barely or not indicated in the dorsal view; the aedeagus, with the phallobase clearly longer than the parameres, which are regularly narrowed from the base to the apex.</p> <p>In the northern limit of its distribution area (Marismas del Odiel), there is a population differentiable of the type form by the larger average size, a somewhat more robust body, the shinier tegument and a more intense black; pronotum slightly more transverse, with the base curve and less prolonged backwards, and the punctures denser and more marked; elytra without traces of streaks, with the base wider and slightly convergent almost in a straight line towards the scutellum; finally, by the aedeagus, slightly larger and more robust and with the phallobase proportionally somewhat shorter than in the typical form.</p> <p> <b>Geographic distribution:</b> Species described from Doñana National Park (Huelva) and extended on the littoral and sub littoral areas in the southwest of the Iberian Peninsula, from the mouth of Guadalquivir River to the Odiel marsh, being particularly abundant in the typical locality (Bujalance <i>et al.</i> 2016).</p>Published as part of <i>Bujalance, José L., Ferrer, Julio & Cárdenas, Ana M., 2023, A taxonomic revision of the genus Tentyria Latreille, 1802 in the Iberian Peninsula and Balearic Islands (Coleoptera: Tenebrionidae), pp. 1-88 in Zootaxa 5320 (1)</i> on pages 45-46, DOI: 10.11646/zootaxa.5320.1.1, <a href="http://zenodo.org/record/8203747">http://zenodo.org/record/8203747</a>
Tentyria corrugata Rosenhauer, J. Ferrer 1856
<i>Tentyria corrugata</i> Rosenhauer, 1856 (Figs. 25, 59, 93, 94, 130, 177, 211, 242, 243) <p> <i>Tentyria corrugata</i> Rosenhauer, 1856: 189; Kraatz 1865: 143–144, Reitter 1900: 175 (specimens from Spain), Fuente 1934: 31, Koch 1944a: 228, Español 1960: 407, L̂bl & Smetana 2008: 206, Martínez 2008: 58, Ivan & L̂bl 2020: 249. <i>Tentyria gaditana</i> ssp. <i>corrugata</i> Rosenhauer Viñolas 1986: 104, Viñolas & Cartagena 2005: 81, 357b. <i>Tentyria andalusiaca</i> Kraatz, 1865: 142, Koch 1944a: 227 syn. “ <i>andalusica</i> ”, Español 1960: 407, Viñolas 1986: 104, L̂bl & Smetana 2008: 206, Martínez 2018: 58, Ivan & L̂bl 2020: 249.</p> <p> <b>Types examined:</b> Two syntypes uncatalogued from the MNHN, carrying the following old labels: <i>Tentyria corrugata</i> Rosh. / Málaga / Ex. Musaeo Rosenhauer / LECTOTYPE, <i>Tentyria corrugata</i> Rosh., det. J. Ferrer & J.L. Bujalance, ex. Coll. Oberthür via Allard MNHN (1♀ MNHN); Ex. Musaeo Rosenhauer / Paralectotype, <i>Tentyria gaditana</i> Rosh. (error! “ <i>Tentyria corrugata</i> Rosh. ”), ex. Coll. Oberthür vía Allard MNHN (1♁ MNHN). Two syntypes of <i>Tentyria andalusiaca</i> Kraatz syn. bearing the following labels: Andalus. Stauding / coll. Kraatz / SYNTYPUS / <i>andalusiaca</i> Kr., Type, det. Schuster / Coll. DEI, Münchenberg/ <i>andalusiaca</i> Kr. / <i>andalusiaca</i> Kr. / LECTOTYPUS <i>Tentyria andalusiaca</i> Kr., J.L. Bujalance det. 2005 (1♁, SDEI); another syntype with the first five labels identical / PARALECTOTYPUS. J.L. Bujalance det. (1♁, SDEI).</p> <p> <b>Additional material: Historical material:</b> Andalusia: Cádiz: Tarifa, V.1903, Escalera leg., <i>Tentyria corrugata</i> Rosenh., (2 exx, MNCN).</p> <p> Málaga: Málaga, 5.VII.1966, F. Español leg., <i>Tentyria corrugata</i> Rosh., F. Español det. (2 exx, CJF); Fuengirola, 16.I.1965, J. Ferrer leg., <i>Tentyria corrugata</i> Ros. (1♀ CJF and 1♁ CJLB); idem, río, 7.5.1977, idem, (1 ex, CJF); idem, 7.XI.1962, S. Aberg leg., <i>Tentyria corrugata</i> Rosh., J.L. Bujalance det. (1♀ NHMS); Estepona, IV.1955, Gyllensvärd leg., <i>corrugata</i> Rosenhauer, J. Ferrer det., CUM TYPO COMP. (1♁, NHMS).</p> <p> <b>Diagnosis</b>: Body (Fig. 211) convex, broad, and robust, integument dull black. Head (Fig. 25) with thin but dense punctures, with eyes very flat not overflowing lateral outline, supraorbital keel slightly raised; anterior edge of epistome rounded and with a minute tooth in the middle; gular groove (Fig. 59) consisting of a median depression, moderately deep and not delimited. Pronotum transverse (Figs. 93, 94), 1.3 to 1.4 times wider than long, finely but densely punctured, strongly rounded at sides, tapering evenly towards both ends, finely marginate, more strongly delimited at base, posterior angles obtuse and little or no marked in dorsal view, with base variable, from slightly curved to strongly curved and extended backwards. Prosternal apophysis with parallel sides and blunt tip (Fig. 130); the male protibiae is somewhat more graceful than those of females and with the inner edge slightly sinuous. Elytra ovate, with maximum width in the middle, tapering almost equally towards the base and apex, striated-rough, with wide intervals but, blurred by tuberous transverse wrinkles, with very fine and spaced punctures; the base is usually in arc; Aedeagus robust, with the parameters equal or slightly longer than the phallobase (Fig. 177).</p> <p> <b>Comments:</b> <i>T. corrugata</i> Rosenhauer is morphologically and geographically close to <i>T. gaditana</i> Rosenhauer, but different in the shape and sculpture of the elytra, the base usually in arc, more angulous humeri; the male protibiae more graceful; usually, more transverse pronotum. Smaller aedeagus, more robust and with the parameters equal or slightly longer than the phallobase. The general shape of the body is also more robust and larger average size.</p> <p> <i>T. corrugata</i> is a well characterised species and unmistakable into the distribution area but was described with a small number of specimens (Rosenhauer 1856) not well reflecting its variability. This fact together with the lack of knowledge of the types by all the authors since Rosenhauer (1856), induced Kraatz (1865) to describe <i>T. andalusiaca</i> Kraatz, with two exemplars from uncertain locality “ Andalucía ” and that correspond to variations of <i>T. corrugata</i> Rosenhauer, as it has been proved after comparing them with the locotipìcal specimens. Reitter (1900), indicated this species from Spain and Portugal. Koch (1944a) established the synonymy between <i>T. andalusica</i> Kraatz, and <i>T. corrugata</i> Rosenhauer, later confirmed by Español (1960). Viñolas (1986) considered <i>T. corrugata</i> Rosenhauer a subespecies of <i>T. gaditana</i> Rosenhauer; nevertheless, these taxa, although close, they have quite differentiable aedeagi. Lastly, Viñolas (1991) and Viñolas & Cartagena (2005), misinterpreted the description of <i>T. andalusiaca</i> Kraatz, and non-having seen the Types, considered it a valid species, only known from southwestern Portugal “Cabo Sardão and Vila Nova Milfontes”. However, the study of the syntypes of <i>Tentyria andalusiaca</i> Kraatz allows confirming the synonymy with <i>T</i>. <i>corrugata</i> Rosenhauer, established by Koch (1944a), being <i>T. andalusiaca</i> sensu Viñolas, an unpublished species (= <i>T. stupefacta</i> <b>sp. nov.</b>), and different from <i>T. andalusiaca</i> Kraatz (= <i>T. corrugata</i> Rosenhauer).</p> <p> <b> Designation of Lectotype of <i>Tentyria corrugata</i> Rosenhauer, 1856. Present designation:</b> </p> <p> The labels carried by the two historical specimens, together with the description of Rosenhauer (1856) fully concordant, indicate that these are two syntypes. For that, we designate Lectotype (Fig. 242) the specimen bearing the following label: <i>Tentyria corrugata</i> Rosh. / Málaga / Ex. Musaeo Rosenhauer / LECTOTYPE, <i>Tentyria corrugata</i> Rosh., Det. J. Ferrer & J.L. Bujalance, ex. Coll. Oberthür via Allard MNHN. Likewise, we designated Paralectotype the specimen bearing the following label: Ex. Musaeo Rosenhauer / Paralectotype, <i>Tentyria gaditana</i> Rosh. (error! “ <i>Tentyria corrugata</i> Rosh. ”), ex. Coll. Oberthür via Allard MNHN.</p> <p> <b> Designation of Lectotype of <i>Tentyria andalusiaca</i> Kraatz, 1865 syn. Present designation:</b> </p> <p> As a result of the confusion of this taxon with a hitherto unpublished species, <i>Tentyria stupefacta</i> <b>sp. nov.</b>, we believe necessary to designate as Lectotype and Paralectotype the two specimens of the Type material (Kraatz 1865: 142). We designate Lectotype (Fig. 243) to the specimen that bears the following labels: Andalus. Stauding / coll. Kraatz / SYNTYPUS / <i>andalusiaca</i> Kr., Type, det. Schuster / Coll. DEI, Münchenberg / <i>andalusiaca</i> Kr., Light blue handwritten / <i>andalusiaca</i> Kr. / LECTOTYPUS <i>Tentyria andalusiaca</i> Kr., J.L. Bujalance des., 2005 (red label). Likewise, we designate Paralectotype to the other syntype that bears the label “ PARALECTOTYPUS. J.L. Bujalance des. 2005 “(red label), in addition to five other labels like the first five described for the Lectotype.</p> <p> <b>Geographical distribution</b>: species described from Malaga, only known from the coast of the provinces of Malaga to Tarifa (Cádiz).</p>Published as part of <i>Bujalance, José L., Ferrer, Julio & Cárdenas, Ana M., 2023, A taxonomic revision of the genus Tentyria Latreille, 1802 in the Iberian Peninsula and Balearic Islands (Coleoptera: Tenebrionidae), pp. 1-88 in Zootaxa 5320 (1)</i> on pages 44-45, DOI: 10.11646/zootaxa.5320.1.1, <a href="http://zenodo.org/record/8203747">http://zenodo.org/record/8203747</a>
Mémoires critiques sur l' Orient suivis de réflexions philosophiques, et dun essai sur l'ile de Corfou. Par M. le comte de Ferrer. Ancien capitaine d' Articlerie de marine. Paris Firmin didot, Frères. rue Jacob, 24 1847.
Preface: by Ferrer,Dedication:Content description: TitleIllustration: 1 (Maps ,)Pagination: PP7+245P+1PPVolumes: 1Text Genre:ProseIllustration: 1 (χάρτες ,
What is the type of Scilla maritima?
The lectotype of the name Scilla maritima L. was designated by Ferrer-Gallego in 2013
and is the specimen, herbarium Adriaan van Royen No. 913.62-327 (L, barcode L 0052807) preservet in
the van Royen’s collection at Leiden. The “typification” proposed by Mario Martínez-Azorín, Manuel B.
Crespo and M. Ángeles Alonso-Vargas in 2022 is superfluous and ineffective according to the
International Code of Nomenclature for algae, fungi, and plants (Shenzhen Code).El lectotipo del nombre Scilla maritima L. fue designado por Ferrer-Gallego en 2013 a partir de un espécimen conservado en herbario Adriaan van
Royen nº 913.62-327 (L, código de barras L 0052807) en la colección de van Royen en Leiden. La
tipificación recientemente propuesta por M. Martínez-Azorín, M.B. Crespo y M.Á. Alonso-Vargas en
2022 es superflua e inefectiva de acuerdo al Código Internacional de Nomenclatura para algas, hongos, y
plantas (Código de Shenzhen)
Autonomous Artificial Nanomotor Powered by Sunlight
Light excitation powers the reversible shuttling movement of the ring component of a rotaxane between two stations located at a 1.3-nm distance on its dumbbell-shaped component. The photoinduced shuttling movement, which occurs in solution, is based on a "four-stroke" synchronized sequence of electronic and nuclear processes. At room temperature the deactivation time of the high-energy charge-transfer state obtained by light excitation is approximate to 10 mu s, and the time period required for the ring-displacement process is on the order of 100. mu s. The rotaxane behaves as an autonomous linear motor and operates with a quantum efficiency up to approximate to 12%. The investigated system is a unique example of an artificial linear nanomotor because it gathers together the following features: (i) it is powered by visible light (e.g., sunlight); (h) it exhibits autonomous behavior, like motor proteins; (iii) it does not generate waste products; (iv) its operation can rely only on intramolecular processes, allowing in principle operation at the single-molecule level; (v) it can be driven at a frequency of 1 kHz; (vi) it works in mild environmental conditions (i.e., fluid solution at ambient temperature); and (vii) it is stable for at least 10(3) cycles.Balzani, V.; Clemente-Leon, M.; Credi, A.; Ferrer Ribera, RB.; Venturi, M.; Flood, A.; Stoddart, J. (2006). Autonomous artificial nanomotor powered by sunlight. Proceedings of the National Academy of Sciences. 103(5):1178-1183. doi:10.1073/pnas.0509011103S117811831035Balzani, V., Credi, A., Raymo, F. M., & Stoddart, J. F. (2000). Artificial Molecular Machines. Angewandte Chemie, 39(19), 3348-3391. doi:10.1002/1521-3773(20001002)39:193.0.co;2-xMolecular Machines Special Issue. (2001). Accounts of Chemical Research, 34(6), 409-409. doi:10.1021/ar0100881Joachim, C., & Gimzewski, J. K. (s. f.). Single Molecular Rotor at the Nanoscale. Structure and Bonding, 1-18. doi:10.1007/3-540-44421-1_1Balzani, V., Credi, A., Ferrer, B., Silvi, S., & Venturi, M. (s. f.). Artificial Molecular Motors and Machines: Design Principles and Prototype Systems. Topics in Current Chemistry, 1-27. doi:10.1007/128_008Oster, G., & Wang, H. (2003). Rotary protein motors. Trends in Cell Biology, 13(3), 114-121. doi:10.1016/s0962-8924(03)00004-7Lehn, J.-M. (2002). Toward complex matter: Supramolecular chemistry and self-organization. Proceedings of the National Academy of Sciences, 99(8), 4763-4768. doi:10.1073/pnas.072065599Steinberg-Yfrach, G., Rigaud, J.-L., Durantini, E. N., Moore, A. L., Gust, D., & Moore, T. A. (1998). Light-driven production of ATP catalysed by F0F1-ATP synthase in an artificial photosynthetic membrane. Nature, 392(6675), 479-482. doi:10.1038/33116Kelly, T. R., De Silva, H., & Silva, R. A. (1999). Unidirectional rotary motion in a molecular system. Nature, 401(6749), 150-152. doi:10.1038/43639Koumura, N., Zijlstra, R. W. J., van Delden, R. A., Harada, N., & Feringa, B. L. (1999). Light-driven monodirectional molecular rotor. Nature, 401(6749), 152-155. doi:10.1038/43646Brouwer, A. M. (2001). Photoinduction of Fast, Reversible Translational Motion in a Hydrogen-Bonded Molecular Shuttle. Science, 291(5511), 2124-2128. doi:10.1126/science.1057886Badjic, J. D. (2004). A Molecular Elevator. Science, 303(5665), 1845-1849. doi:10.1126/science.1094791Hernandez, J. V. (2004). A Reversible Synthetic Rotary Molecular Motor. Science, 306(5701), 1532-1537. doi:10.1126/science.1103949Mobian, P., Kern, J.-M., & Sauvage, J.-P. (2004). Light-Driven Machine Prototypes Based on Dissociative Excited States: Photoinduced Decoordination and Thermal Recoordination of a Ring in a Ruthenium(II)-Containing[2]Catenane. Angewandte Chemie International Edition, 43(18), 2392-2395. doi:10.1002/anie.200352522Sherman, W. B., & Seeman, N. C. (2004). A Precisely Controlled DNA Biped Walking Device. Nano Letters, 4(7), 1203-1207. doi:10.1021/nl049527qAstumian, R. D. (2005). Chemical peristalsis. Proceedings of the National Academy of Sciences, 102(6), 1843-1847. doi:10.1073/pnas.0409341102Zheng, X., Mulcahy, M. E., Horinek, D., Galeotti, F., Magnera, T. F., & Michl, J. (2004). Dipolar and Nonpolar Altitudinal Molecular Rotors Mounted on an Au(111) Surface. Journal of the American Chemical Society, 126(14), 4540-4542. doi:10.1021/ja039482fKatz, E., Lioubashevsky, O., & Willner, I. (2004). Electromechanics of a Redox-Active Rotaxane in a Monolayer Assembly on an Electrode. Journal of the American Chemical Society, 126(47), 15520-15532. doi:10.1021/ja045465uVan Delden, R. A., ter Wiel, M. K. J., Pollard, M. M., Vicario, J., Koumura, N., & Feringa, B. L. (2005). Unidirectional molecular motor on a gold surface. Nature, 437(7063), 1337-1340. doi:10.1038/nature04127Liu, Y., Flood, A. H., Bonvallet, P. A., Vignon, S. A., Northrop, B. H., Tseng, H.-R., … Stoddart, J. F. (2005). Linear Artificial Molecular Muscles. Journal of the American Chemical Society, 127(27), 9745-9759. doi:10.1021/ja051088pNguyen, T. D., Tseng, H.-R., Celestre, P. C., Flood, A. H., Liu, Y., Stoddart, J. F., & Zink, J. I. (2005). A reversible molecular valve. Proceedings of the National Academy of Sciences, 102(29), 10029-10034. doi:10.1073/pnas.0504109102Berná, J., Leigh, D. A., Lubomska, M., Mendoza, S. M., Pérez, E. M., Rudolf, P., … Zerbetto, F. (2005). Macroscopic transport by synthetic molecular machines. Nature Materials, 4(9), 704-710. doi:10.1038/nmat1455Tian, Y., & Mao, C. (2004). Molecular Gears: A Pair of DNA Circles Continuously Rolls against Each Other. Journal of the American Chemical Society, 126(37), 11410-11411. doi:10.1021/ja046507hAshton, P. R., Ballardini, R., Balzani, V., Credi, A., Dress, K. R., Ishow, E., … Wenger, S. (2000). Chemistry - A European Journal, 6(19), 3558-3574. doi:10.1002/1521-3765(20001002)6:193.0.co;2-
L-Serine biosensor-controlled fermentative production of L-tryptophan derivatives by Corynebacterium glutamicum
Ferrer L, Elsaraf M, Mindt M, Wendisch VF. L-Serine biosensor-controlled fermentative production of L-tryptophan derivatives by Corynebacterium glutamicum. Biology. 2022;11(5): 744.l-Tryptophan derivatives, such as hydroxylated or halogenated l-tryptophans, are used in therapeutic peptides and agrochemicals and as precursors of bioactive compounds, such as serotonin. l-Tryptophan biosynthesis depends on another proteinogenic amino acid, l-serine, which is condensed with indole-3-glycerophosphate by tryptophan synthase. This enzyme is composed of the α-subunit TrpA, which catalyzes the retro-aldol cleavage of indole-3-glycerol phosphate, yielding glyceraldehyde-3-phosphate and indole, and the β-subunit TrpB that catalyzes the β-substitution reaction between indole and l-serine to water and l-tryptophan. TrpA is reported as an allosteric actuator, and its absence severely attenuates TrpB activity. In this study, however, we showed that Corynebacterium glutamicum TrpB is catalytically active in the absence of TrpA. Overexpression of C. glutamicumtrpB in a trpBA double deletion mutant supported growth in minimal medium only when exogenously added indole was taken up into the cell and condensed with intracellularly synthesized l-serine. The fluorescence reporter gene of an l-serine biosensor, which was based on the endogenous transcriptional activator SerR and its target promoter PserE, was replaced by trpB. This allowed for l-serine-dependent expression of trpB in an l-serine-producing strain lacking TrpA. Upon feeding of the respective indole derivatives, this strain produced the l-tryptophan derivatives 5-hydroxytryptophan, 7-bromotryptophan, and 5-fluorotryptopha
CAJA 145 - LEGAJO I - SIGNATURA 08
La Comisión de Agricultura, a propuesta de D. Vicente Ferrer y Fuertes, decide elevar a S. M. una exposición manifestando los graves perjuicios sufridos por el arbolado de la provincia por las nieves pasadas y pidiendo se haga rebaja de contribuciones a los propietarios que hayan sufrido estas pérdidas.Ferrer Y Fuertes, V. (1860). La Comisión de Agricultura, a propuesta de D. Vicente Ferrer y Fuertes, decide elevar a S. M. una exposición manifestando los graves perjuicios sufridos por el arbolado de la provincia por las nieves pasadas y pidiendo se haga rebaja de contribuciones a l. Real Sociedad Económica de Amigos del País de Valencia. https://riunet.upv.es/handle/10251/22828Importación Masiv
Breue compendium quaestionu quae aeueniunt in praxi in materia Fiscali coram iudicibus Fisci sanctae Inquisicionis
Datos de pie de imprenta tomados de colofónSign.: A-I\p8\s, L-M\p8\sError de fol. de la h. 64 pasa a la 67Port. con esc. episcopal xil. de Fernando de Valdés, Arzobispo de Sevilla, a quien va dedicada la obr
- …
