The genera Stegastopsis Kraatz, 1865 and Orostegastopsis Koch, 1962 with description of O. planioculata sp. n. from Oman (Coleoptera: Tenebrionidae: Tentyriini)

The first Asian member of Orostegastopsis Koch, 1962 Koch, C. (1962): Vierter taxonomischer Beitrag zur Kenntnis der Tenebrioniden Somalias: Über die von Prof. G. Scortecci 1953 und 1957 in der Migiurtinia-Provinz gesammelten Arten. 1. Teil. Atti della Società Italiana di Scienze Naturali, 51, 237–270. [Google Scholar] is described and figured: O. planioculata sp. n., which can be easily distinguished from the two Somalian species O. scorteccii Koch, 1962 Koch, C. (1962): Vierter taxonomischer Beitrag zur Kenntnis der Tenebrioniden Somalias: Über die von Prof. G. Scortecci 1953 und 1957 in der Migiurtinia-Provinz gesammelten Arten. 1. Teil. Atti della Società Italiana di Scienze Naturali, 51, 237–270. [Google Scholar] and O. kaszabi (Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) comb. nov. by the shallow eyes. According to the shape of the clypeus, Stegastopsis kaszabi Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar] is transferred from the genus Stegastopsis Kraatz to the genus Orostegastopsis Koch as was already indicated by Bremer (1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) who treated Orostegastopsis as a subgenus of Stegastopsis: Orostegastopsis kaszabi (Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) comb. nov. Keys to the species of Stegastopsis and Orostegastopsis are given.     

Molecular characterisation of four echinostomes (Digenea: Echinostomatidae) from birds in New Zealand,with descriptions of <Emphasis Type="Italic">Echinostoma novaezealandense</Emphasis> n. sp. and <Emphasis Type="Italic">Echinoparyphium poulini</Emphasis> n. sp.

Morphological and molecular characterisation of echinostome specimens (Digenea: Echinostomatidae) recovered in one Anas platyrhynchos L. and one Cygnus atratus (Latham) (Anseriformes: Anatidae) from New Zealand revealed the presence of two known species, Echinostoma miyagawai Ishii, 1932 and Echinoparyphium ellisi (Johnston & Simpson, 1944) and two species new to science. Comparative morphological and phylogenetic analyses supported the distinct species status of Echinostoma novaezealandense n. sp. ex Branta canadensis (L.), A. platyrhynchos and C. atratus, and Echinoparyphium poulini n. sp. ex C. atratus. Echinostoma novaezealandense n. sp., a species of the “revolutum” species complex characterised by the possession of a head collar armed with 37 spines, keyed down to E. revolutum but was distinguished from the latter in having a much narrower body with almost parallel margins, longer oesophagus, wider cirrus-sac, larger seminal vesicle, much smaller ventral sucker, ovary, Mehlis’ gland and testes, more anteriorly located ovary and testes, and distinctly smaller eggs (81–87 × 42–53 vs 106–136 × 55–70 µm). This new species appears similar to Echinostoma acuticauda Nicoll, 1914 described in Australia but differs in having a longer forebody, more posteriorly located ovary and testes, and much smaller eggs (81–87 × 42–53 vs 112–126 × 63–75 µm). Echinoparyphium poulini n. sp. is differentiated from the four species of Echinoparyphium possessing 37 collar spines considered valid as follows: from E. chinensis Ku, Li & Chu, 1964 in having a much smaller body, four (vs five) angle spines and simple seminal vesicle (vs bipartite); from E. schulzi Matevosyan, 1951 in having a less robust body at a comparable body length, much smaller ventral sucker, ovary and testes, and longer but narrower eggs (87–109 × 50–59 vs 70–85 × 60–84 µm); and from the two smaller forms, E. serratum Howell, 1968 and E. aconiatum Dietz, 1909, in a number of additional metrical features correlated with body size and especially in the possession of much larger collar spines. Partial fragments of the mitochondrial nad1 and 28S rRNA genes were amplified for representative isolates of the four species and analysed together with sequences for Echinostoma spp. and Echinoparyphium spp. available on GenBank. Phylogenetic analyses based on the mitochondrial nad1 gene revealed congruence between the molecular data and species identification/delineation based on morphology; this was corroborated by the 28S rDNA sequence data.     

Recombinant production and characterization of an N-acyl-d-amino acid amidohydrolase from Streptomyces sp. 64E6

N-Acyl-d-amino acid amidohydrolases (d-aminoacylases) are often used as tools for the optical resolution of d-amino acids, which are important products with applications in industries related to medicine and cosmetics. For this study, genes encoding d-aminoacylase were cloned from the genomes of Streptomyces spp. using sequence-based screening. They were expressed by Escherichia coli and Streptomyces lividans. Almost all of the cell-free extracts exhibit hydrolytic activity toward N-acetyl-(Ac-)d-Phe (0.05–6.32 μmol min^?1 mg^?1) under conditions without CoCl₂. Addition of 1 mM CoCl₂ enhanced their activity. Among them, the highest activity was observed from cell-free extracts prepared from S. lividans that possess the d-aminoacylase gene of Streptomyces sp. 64E6 (specific activities were, respectively, 7.34 and 9.31 μmol min^?1 mg^?1 for N-Ac-d-Phe and N-Ac-d-Met hydrolysis). Furthermore, when using glycerol as a carbon source for cultivation, the recombinant enzyme from Streptomyces sp. 64E6 was produced in 4.2-fold greater quantities by S. lividans than when using glucose. d-Aminoacylase from Streptomyces sp. 64E6 showed optimum at pH 8.0–9.0. It was stable at pH 5.5–9.0 up to 30 °C. The enzyme hydrolyzed various N-acetyl-d-amino acids that have hydrophobic side chains. In addition, the activity toward N-chloroacetyl-d-Phe was 2.1-fold higher than that toward N-Ac-d-Phe, indicating that the structure of N-acylated portion of substrate altered the activity.     

Cryptic diversity among the achaetous Marionina (Annelida,Clitellata, Enchytraeidae)

This study investigates the diversity and taxonomy of a mainly marine group of species lacking chaetae currently assigned to the genus Marionina. This achaetous group includes four nominal species: M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 12–13.  [Google Scholar]), M. achaeta sensu Lasserre, 1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 87–91.  [Google Scholar], M. nevisensis Righi & Kanner, 1979 Righi, G. and Kanner, E. 1979. Marine Oligochaeta (Tubificidae and Enchytraeidae) from the Caribbean Sea. Studies of the Fauna of Curaçao and other Caribbean Islands, 58: 44–68.  [Google Scholar] and M. arenaria Healy, 1979 Healy, B. 1979a. Marine fauna of County Wexford. 1 – Littoral and brackishwater Oligochaeta. The Irish Naturalists' Journal, 19: 418–422.  [Google Scholar]. As Lasserre's (1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 87–91.  [Google Scholar]) M. achaeta appears to be morphologically different from its (then) senior homonym M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 12–13.  [Google Scholar]), the replacement name M. nothachaeta nom. nov. is proposed for it. We studied the genetic and morphological diversity of achaetous specimens of Marionina collected in Florida, the Great Barrier Reef, New Caledonia, Sweden, England and the Bahamas. The collection localities are almost all supralittoral and often brackish-water habitats. Parts of the mitochondrial genes 12S, 16S, COI and the nuclear genes 18S, 28S and ITS were analysed to assess the genetic variation and phylogeny of the achaetous Marionina species. The molecular data reveal one monophyletic group of 11 separately evolving lineages, and between these lineages, K2P distances in the barcoding gene COI vary between 5.4 and 25.0%. On a morphological basis, the lineages could be assigned to seven different groups (morphotypes), of which only two could be identified as described nominal taxa: M. nevisensis s. lat. (several lineages) and M. nothachaeta. Since the former taxon appears to be a complex of cryptic species around the world and the original type material no longer exists, a neotype from the Caribbean was designated for M. nevisensis s. str. The remaining achaetous lineages represent five morphologically distinct species that are left unnamed, awaiting finer morphological scrutiny and detailed comparisons with new collections of M. achaeta and M. arenaria. Summing up, the group of achaetous Marionina now seems to contain up to 13 different species, seven of which are yet to be formally described and named.     

Taxonomy,morphology and molecular systematics of a new oligotrich ciliate,Williophrya maedai gen. nov., sp. nov., with redescriptions of Strombidium basimorphum and Pseudotontonia simplicidens (Protozoa,Ciliophora, Oligotrichia)

The morphology and small subunit rRNA (SSrRNA) gene sequence of a marine oligotrich ciliate, Williophrya maedai gen. nov., sp. nov., are reported. The new genus Williophrya is characterized by the adoral zone with no differentiation of membranelles, and the reduced somatic ciliature which comprises a bipartite girdle kinety only. In addition, the in vivo morphologies of two other oligotrichs, namely Strombidium basimorphum Martin & Montagnes, 1993 and Pseudotontonia simplicidens (Lynn & Gilron, 1993 Lynn, D. H. and Gilron, G. L. 1993. Strombidiid ciliates from coastal waters near Kingston Harbour, Jamaica (Ciliophora, Oligotrichia, Strombidiidae). Journal of the Marine Biological Association of the United Kingdom, 73: 47–65. [Crossref] , [Google Scholar]) Agatha, 2004, are reported for the first time based on Chinese populations. Improved diagnoses of both species are supplied. The phylogenetic position of Williophrya maedai is investigated based on SSrRNA gene sequence data. These show that: (1) Williophrya maedai is most closely related to Strombidium purpureum and S. apolatum; (2) Williophrya is assigned to the family Strombidiidae although it has some unique morphological features regarding its oral and somatic ciliatures.     

Restrictions on the Production of Multi-Wall Carbon Nanotubes and Nanofibers by Gallionella sp.

The enzymatic oxidization of dissolved Fe(II) to Fe(III) by neutrophilic Fe-oxidizing bacteria plays a significant role in biological cycling of iron by inducing the precipitation of Fe(III) oxyhydroxide in aqueous environments. Among the diverse neutrophilic Fe-oxidizing bacteria, the genus Gallionella has received wide attention for its production of unique twisted extracellular stalks. Hallberg and Tai (2014 Hallberg R, Tai CW. 2014. Multi-wall carbon nanotubes and nanofibers in Gallionella. Geomicrobiol J 31(9):764–768.[Taylor & Francis Online], [Web of Science ®] , [Google Scholar]) recently reported the detection of multi-wall carbon nanotubes on the twisted-stalks, and they viewed those carbon nanotubes as being biologically produced by Gallionella. We scrutinized Gallionella-produced biofilms collected from natural environments by scanning electron microscopy and high-resolution transmission electron microscopy. Ferrihydrite and lepidocrocite were the only nano-scaled minerals observed on the stalk, while there were nanometer-sized sheet-like graphitic contaminants on the grid in the vicinity of the sample which showed the same morphology as Hallberg and Tai (2014 Hallberg R, Tai CW. 2014. Multi-wall carbon nanotubes and nanofibers in Gallionella. Geomicrobiol J 31(9):764–768.[Taylor & Francis Online], [Web of Science ®] , [Google Scholar]) observed. Moreover, similar materials on an empty grid and a grid loaded with randomly selected synthesized materials were also observed. Based on the current knowledge of carbon nanotube syntheses, none of the three known synthesizing methods including root-growth, rolling-up and bottom-up could be biochemically produced by any life because of the significant kinetic and energy obstacles. The carbon nanomaterials reported by Hallberg and Tai (2014 Hallberg R, Tai CW. 2014. Multi-wall carbon nanotubes and nanofibers in Gallionella. Geomicrobiol J 31(9):764–768.[Taylor & Francis Online], [Web of Science ®] , [Google Scholar]) were clearly contaminations from amorphous carbon film on the grids for holding samples for transmission electron microscopic observations.     

A revision of fossil eagle owls (Aves: Strigiformes: Bubo) from Europe and the description of a new species,Bubo ibericus,from Cal Guardiola (NE Iberian Peninsula)

The European fossil record of eagle owls, genus Bubo Duméril 1806 Duméril AMC. 1806. Zoologie Analytique, ou Méthode Naturelle de Classification des Animaux, rendue plus Facile à l’Aide de Tableaux Synoptiques. Paris: H. L. Perronneau. [Google Scholar], is thought to extend back into the Miocene, but records of Bubo before the Middle Pleistocene are scarce and mainly constituted by non-diagnostic or fragmentary specimens. Apart from a number of fossil species of Bubo of uncertain validity, i.e. Bubo? florianae Kretzoi 1957 Kretzoi M. 1957. Bird remains from the Hipparion-fauna of Csákvár. Aquila. 63:239–248. [Google Scholar], Bubo lignitum Giebel 1860 Giebel CG. 1860. Zur Fauna der Braunkohlen Formation von Rippersroda in Thüringen. Zeitschrift für die Gesammten Naturwissenschaften. 16:147–153. [Google Scholar], and Bubo perpastus (Ballman 1976 Ballmann P. 1976. Fossile Vögel aus dem Neogen der Halbinsel Gargano (Italien). Zweiter Teil Scripta Geol. 38:1–59. [Google Scholar]), most fossil Bubo material is unassigned to species or assigned to the extant Bubo bubo (Linnaeus 1758) on the basis of size, especially for Early Pleistocene records. Given the ambiguity about the validity of the earliest records, here we revise the pre-Middle Pleistocene fossil record of Bubo in Europe. Our results indicate that, in Europe, Bubo is first recorded in the Late Pliocene/Early Pleistocene of Italy. By the Early Pleistocene, three taxa can be distinguished: Bubo ibericus sp. nov. from Cal Guardiola (Spain), Bubo sp. nov. indet. from Soave Cava Sud (Italy) and Bubo sp. from various sites across Europe. By the Middle Pleistocene, Eurasian environments experienced a substantial increase in severity and duration of glacial periods which might have led to the replacement of extinct species of Bubo by the recent B. bubo and Bubo scandiacus.     

Redefinition of the hypotrichous ciliate Uncinata,with descriptions of the morphology and phylogeny of three urostylids (Protista,Ciliophora)

We investigated the morphology, morphogenesis and small subunit rRNA gene-based phylogeny of three marine urostylids, Uncinata gigantea Bullington, 1940 Bullington, W. E. (1940). Some ciliates from Tortugas. Papers from the Tortugas Laboratory, 32, 179–221. [Google Scholar], Holosticha heterofoissneri Hu & Song, 2001 Hu, X., & Song, W. (2001). Morphology and morphogenesis of Holosticha heterofoissneri n. sp. from the Yellow Sea, China (Ciliophora, Hypotrichida). Hydrobiologia, 448, 171–179. doi:10.1023/A:1017553406031.[Crossref], [Web of Science ®] , [Google Scholar], and Holosticha cf. heterofoissneri. The dorsal morphogenesis of Uncinata gigantea shows de novo formation of two groups of anlagen near the marginal rows. Holosticha cf. heterofoissneri demonstrates fragmentation of the first dorsal kinety anlage as in Holosticha heterofoissneri. Our population of H. heterofoissneri corresponds well with previously described populations in terms of its general morphology and ciliary pattern. Uncinata gigantea can be recognized by its large and highly contractile body, yellowish to brownish cell colour, two types of cortical granules, and 20–30 transversely oriented and densely arranged cirri in the left marginal row, which often overlie the buccal vertex. Based on the new data, especially infraciliature, the genus Uncinata is here redefined. Both the morphology and phylogenetic analyses suggest that the genus Uncinata should be classified within the family Urostylidae. In addition, both morphological and morphogenetic data suggest that Holosticha bradburyae Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar] should be transferred to Uncinata as U. bradburyae (Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar]) comb. nov., due to its possession of a characteristically prominent beak-like, leftwards curved projection and the developmental mode of the dorsal kineties. This assignment is supported by the phylogenetic analyses, which placed Uncinata gigantea in a clade with U. bradburyae (Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar]) comb. nov., and revealed only 1.13% (19 bp) difference in their SSU-rDNA gene sequence.     

A new species of Micragasma J. Sahlberg, 1900 (Coleoptera: Hydraenidae) from Crete

We describe a new species of Micragasma J. Sahlberg, 1900 (Coleoptera, Hydraenidae), which is here treated as a subgenus of Ochthebius Leach, 1815 Leach, W.E. (1815), ‘Entomology’, in The Edinburgh Encyclopaedia (Vol. 9), ed. D. Brewster, Balfour: Edinburgh, pp. 57–172. [Google Scholar]. The new species, O. (Micragasma) minoicus sp. n., was found at the margins of a coastal rockpool in the island of Crete. The species differs from the other two known species of Micragasma in both external and genital characters, but shares with them the presence of small setiferous tubercles on the surface of the head, pronotum and elytra, and a strong medial gibbosity on the head. In some characters, such as the structure and shape of the aedeagus, O. (M.) minoicus sp. n. is similar to other species of the genus Ochthebius, in particular of the subgenus Cobalius Rey, 1886 Rey, C. (1886), ‘Histoire naturelle des coléoptères de France (suite)’, Annales de la Société Linnéenne de Lyon, 32, 1–187, pl. 1–2.[Crossref] , [Google Scholar], typical of coastal rockpools.

http://zoobank.org/urn:lsid:zoobank.org:act:BCEAE1EE-7C5E-4017-A753-559738221502     

Revisiting Lepidonella Yosii (Collembola: Paronellidae): character overview,checklist of world species and reassessment of Pseudoparonella doveri Carpenter

Characters used in the taxonomy of the genus Lepidonella Yosii, 1960 (Collembola: Paronellidae) are listed and discussed. Several new ones are introduced. An overview of pseudopore patterns across Collembola is presented, with several new locations of these structures across Entomobryomorpha. Their interest at different taxonomic level is underlined. The genus Lepidonella is redefined. The American species L. marimuti Soto Adames &; Bellini, 2015 Soto-Adames FN, Bellini BC. 2015. Dorsal chaetotaxy of neotropical species supports a basal position for the genus Lepidonella among scaled Paronellidae (Collembola, Entomobryoidea). Florida Entomologist. 98(1):330–341.[Crossref], [Web of Science ®] , [Google Scholar] is placed in incertae sedis among Lepidonella. Lepidonella species of the world are listed with synonymies and combinations. The Malaysian troglobitic species Pseudoparonella doveri Carpenter, 1933 Carpenter GH. 1933. XIX. Fauna of the Batu caves, Selangor. Journal of the Federated Malay States Museum. 17:217–221. [Google Scholar] is redescribed in detail, with emphasis on its pattern of antennal chaetae, and transferred to the genus Lepidonella. Its close similarity with L. lecongkieti Deharveng &; Bedos, 1995 Deharveng L, Bedos A. 1995. Lepidonella lecongkieti n.sp., premier Collembole cavernicole du Vietnam (Collembola, Paronellidae). Bulletin de la Société entomologique de France. 100(1):21–24. [Google Scholar] from southwestern Vietnam caves is underlined. This disjunct distribution is briefly discussed.     

Spirodesmos milanai n. isp.: A Shallow-Water Spiral Trace Fossil from the Cambrian of the Eastern Cordillera,Northwest Argentina

Abstract

A new ichnofossiliferous locality in Salta Province (northwest Argentina) contains an association with numerous irregular spiral traces assigned to Spirodesmos milanai n. isp., in mature sandstones and quartzites with rippled bedding surfaces, rare wavy lamination and cross-bedded stratification. This record of early spiral behavior is interpreted as a primitive grazing method formed on muddy laminae above sand layers, and is related to a feeding strategy of an annelid-type of organism. Associated traces are Cruziana cf. semiplicata, Diplocraterion isp., Monocraterion isp., Rusophycus isp., Skolithos linearis Haldeman and Skolithos magnus Howell. The ichnoassemblage is similar to a shallow-water ichnoassociation from the Permian Ecca Group of South Africa (Mason et al., 1983 Mason, T. R., Stanistreet, I. G. and Tavener-Smith, R. 1983. Spiral trace fossils from the Permian Ecca Group of Zululand. Lethaia, 16: 241–247. [Crossref], [Web of Science ®] , [Google Scholar]).     

Diving beetles of the genus Liodessus Guignot, 1953 in Colombia,with description of three new species (Coleoptera: Dytiscidae)

The Colombian species of the diving beetle genus Liodessus Guignot, 1939 Guignot, F. (1939), ‘Contribution à l’étude des Bidessus’, Bulletin de la Société d’Étude des Sciences Naturelles de Vaucluse, 10(4), 51–61. [Google Scholar] are revised. Liodessus bogotensis Guignot, 1953 Guignot, F. (1953), ‘Trente-neuvième note sur les hydrocanthares’, Revue Française d’Entomologie, 20, 109–117. [Google Scholar] is re-described. Three higher altitude species are new to science: Liodessus azufralis sp. n., L. quillacinga sp. n. and L. quimbaya sp. n. We also introduce two new subspecies, L. quillacinga cochaensis ssp. n. and L. quillacinga cumbalis ssp. n. We delineate the species using morphological structures such as male genital structure and beetle size, shape and colour pattern. Mitochondrial cox1 sequence data provided an additional character source. All the new species occur on higher altitudes above 2700 m and were collected in shallow, exposed peatland pools and puddles, mostly in Páramo. Liodessus obscurellus (LeConte, 1852), not yet recorded from Colombia, is included into the key due to its presence in nearby Costa Rica and Ecuador. The known distribution and habitat preferences of each species are outlined briefly.     

The genus Antillophos Woodring, 1928 (Gastropoda: Buccinidae) from the China seas,with description of a new species

The species of genus Antillophos Woodring, 1928 Woodring, W.P. (1928) Miocene Mollusks from Bowden, Jamaica. 2. Gastropods and Discussion of Results. Contributions to the Geology and Paleontology of the West Indies. Carnegie Institute of Washington, Washington D.C. [Google Scholar] from the China seas are studied. Six species, Antillophos liui n. sp., Antillophos lucubratonis Fraussen & Poppe, 2005 Fraussen, K. & Poppe, G.T. (2005) Revision of Phos and Antillophos (Buccinidae) from the Central Philippines. Visaya 1, 76–115. [Google Scholar], Antillophos monsecourorum Fraussen & Poppe, 2005 Fraussen, K. & Poppe, G.T. (2005) Revision of Phos and Antillophos (Buccinidae) from the Central Philippines. Visaya 1, 76–115. [Google Scholar], Antillophos pyladeum (Kato, 1995 Kato, S. (1995) Discussion of the genus Phos. Hitaciobi 70, 15–20. [Google Scholar]), Antillophos roseatus (Hinds, 1844 Hinds, R.B. (1844) Mollusca. In: Hinds, R.B. (Ed.) The Zoology of the Voyage of H.M.S. Sulphur During the years 1836–1842. 2. Smith, Elder and Co., London, pp. 1–72. [Google Scholar]) and Antillophos sp., are described and illustrated.

http://zoobank.org/urn:lsid:zoobank.org:pub:51481997-A841-4F37-8E15-B753DC99CB4D     

Purification, characterization and kinetic properties of extracellular l-asparaginase produced by Cladosporium sp.

l-asparaginase from Cladosporium sp. grown on wheat bran by SSF was purified. Enzyme appeared to be a trimer with homodimer of 37 kDa and another 47 kDa amounting to total mass of 121 kDa as estimated by SDS-PAGE and 120 kDa on gel filtration column. The optimum temperature and pH of the enzyme were 30 °C and 6.3, respectively with Vmax of 4.44 μmol/mL/min and Km of 0.1 M. Substrate specificity studies indicated that, l-asparaginase has greater affinity towards l-asparagine with substrate hydrolysis efficiency (Vmax/Km ratio) eightfold higher than that of l-glutamine. l-asparaginase activity in presence of thiols studied showed decrease in Vmax and increase in Km, indicating nonessential mode of inactivation. Among the thiols tested, β-mercaptomethanol, exerted inhibitory effect, suggesting a critical role of disulphide linkages in maintaining a suitable conformation of the enzyme. Metal ions such as Ca²⁺, Co²⁺, Cu²⁺, Mg²⁺, Na⁺, K⁺ and Zn²⁺ significantly affected enzyme activity whereas presence of Fe³⁺, Pb²⁺ and KI stimulated the activity. Detergents studied also enhanced l-asparaginase activity. In-vitro half-life of purified l-asparaginase in mammalian blood serum was 93.69 h. The enzyme inhibited acrylamide formation in potato chips by 96 % making it a potential candidate for food industry to reduce acrylamide content in starchy fried food commodities.