Intra- and interspecific genetic differentiation in closely related pines fromPinus subsectionSylvestres (Pinaceae) in the former Soviet Union

Thirty-seven natural populations of four closely related species ofPinus subsect.Sylvestres, P. mugo, P. funebris, P. pallasiana, andP. sylvestris, occurring in the former Soviet Union were investigated by starch-gel electrophoresis. In the populations assayed 127 allelic variants at 25 loci were revealed.Nei's distance coefficient (Dn) was used to estimate the level of genetic differentiation amongP. sylvestris races and among closely related species. A dendrogram constructed using Dn values shows that of the fiveP. sylvestris races analyzed only the geographically isolated var.hamata exhibited sufficient differences at theDia-2 locus (a mean Dn value relative to the other four races is 0.025) to recognize it as a distinct taxon. The remaining races, sylvestris, cretacea, lapponica, and sibirica, have a similar gene pool (Dn values are not greater than 0.010), and they should be regarded as a single taxon,P. sylvestris var.sylvestris. Interspecific comparisons revealed thatP. sylvestris andP. mugo have the closest genetic affinities to each other withNei's genetic distance of 0.108. The dendrogram demonstrates thatP. funebris is closer toP. sylvestris andP. mugo thanP. pallasiana. The available paleontologic data allowed us to conclude thatNei's (1975) time scale estimate for the time of divergence of the taxa was more accurate thanNei's (1971) time scale estimate.     

A preliminary phylogeny for the NeotropicalRubiaceae

The sequence of subfamilies,Cinchonoideae, Antirheoideae andRubioideae, attemps to show their natural affinities and phylogeny. The subfamilies are those ofVerdcourt, and the order in which they are presented is that ofBremekamp. A list is presented of the subfamilies, tribes and genera of theRubiaceae to be utilized in the Catálogo Ilustrado de las plantas de Cundinamarca, Colombia.     

Enzymic synthesis of lacto-N-triose II and its positional analogues

N-acetylhexosaminidase fromNocardia orientalis catalysed the synthesis of lacto-N-triose II glycoside (-d-GlcNAc-(1-3)--d-Gal-(1-4)--d-Glc-OMe,3) with its isomers -d-GlcNAc-(1-6)--d-Gal-(1-4)--d-Glc-OMe (4) and -d-Gal-(1-4)-[-d-GlcNAc-(1-6)]--d-Glc-OMe (5) throughN-acetylglucosaminyl transfer fromN,N-diacetylchitobiose (GlcNAc₂) to methyl -lactoside. The enzyme formed the mixture of trisac-charides3, 4 and5 in 17% overall yield based on GlcNAc₂, in a ratio of 20:21:59. Withp-nitrophenyl -lactoside as an acceptor, the enzyme also producedp-nitrophenyl -lacto-N-trioside II (-d-GlcNAc-(1-3)--d-Gal-(1-4)--d-Glc-OC₆H₄NO₂-p,6) with its isomers -d-GlcNAc-(1-6)--d-Gal-(1-4)--d-Glc-OC₆H₄NO₂-p (7) and -d-Gal-(1-4)-[-d-GlcNAc-(1-6)]--d-Glc-OC₆H₄NO₂-p (8). In this case, when an inclusion complex ofp-nitrophenyl lactoside acceptor with -cyclodextrin was used, the regioselectivity of glycosidase-catalysed formation of trisaccharide glycoside was substantially changed. It resulted not only in a significant increase of the overall yield of transfer products, but also in the proportion of the desired compound6.Abbreviations GlcNAc₂ 2-acetamido-2-deoxy--d-glucopyranosyl-(1-4)-2-acetamido-2-deoxy-d-glucose - NAHase N-acetylhexosaminidase - -CD -cyclodextrin     

Sexual compatibility between serotypes ofFilobasidiella neoformans (Cryptococcus neoformans)

Twenty-five of 37Cryptococcus neoformans strains of known serotype produced the basidiomycetousFilobasidiella state either alone or when paired with a strain of compatible mating-type. Sixteen strains were mating-type, four strains were a mating-type, and five strains were self-fertile.F. neoformans serotypes A and D were interfertile with compatible mating-types ofF. bacillispora serotypes B and C.C. neoformans var.gattii was interfertile with compatible mating-types ofF. neoformans andF. bacillispora. F. bacillispora strains, which utilized creatinine andl-malic acid, were interfertile with compatible mating-types ofF. neoformans, which did not utilize creatinine andl-malic acid. The interfertility between serotypes and biotypes eliminates the need for recognizing the names ofC. neoformans var.gattii, C. bacillisporus, andF. bacillispora. It is proposed thatC. neoformans var.gattii andC. bacillisporus be regarded as later, facultative synonyms ofC. neoformans and thatF. bacillispora be regarded as a later, facultative synonym ofF. neoformans.     

What is happening to the monocotyledons?

An attempt is made to elucidate some of the more pronounced departures from traditional classifications in the book The families of the monocotyledons byDahlgren and collaborators, which embodies the latest opinions of the lateRolf Dahlgren on the subject. Consideration is given to the treatment of theLiliiflorae (especiallyLiliales andAsparagales) andBromeliiflorae, and to the theory offered for the origin of the monocots which identifies theDioscoreales as the most primitive order of the subclass.Dahlgren aimed at an eclectic classification (one based on a combination of similarity criteria and phylogenetic criteria) and the results of his use of cladistic methods (in association withF. N. Rasumssen) to supply the phylogenetic input are assessed. The resulting system itself is considered in the light of the distinction drawn byJ. S. L. Gilmour between natural and artificial classifications and their respective uses.Dedicated to the memory of JohnS. L. Gilmour.     

d-Alanine dehydrogenase

Pseudomonas aeruginosa PA01 was found to utilise both thed- andl-isomers of -alanine and also -alanine as sole sources of carbon and energy for growth. Enzymological studies of wild-type cultures and comparison with mutants deficient in growth upon one or more isomers of alanine led to the following conclusions: (i) utilisation ofd-alanine involved its direct oxidation by an inducible, membrane-bound, cytochrome-linked dehydrogenase; (ii) utilisation ofl-alanine required its conversion to the directly oxidisabled-form by a soluble racemase; (iii) utilisation of -alanine, likel-alanine, involves both the racemase andd-alanine dehydrogenase enzymes, but in addition must involve other enzymes the identity, of which is still speculative; (iv)P. aeruginosa, likeEscherichia coli, appears to take upd-alanine andl-alanine by means of two specific permeases.Abbreviation DCPIP 2,6-dichlorophenol-indophenol     

Organization of genes required for gellan polysaccharide biosynthesis in<Emphasis Type="Italic"> Sphingomonas elodea</Emphasis> ATCC 31461

Sphingomonas elodea ATCC 31461 produces gellan, a capsular polysaccharide that is useful as a gelling agent for food and microbiological media. Complementation of nonmucoid S. elodea mutants with a gene library resulted in identification of genes essential for gellan biosynthesis. A cluster of 18 genes spanning 21 kb was isolated. These 18 genes are homologous to genes for synthesis of sphingan polysaccharide S-88 from Sphingomonas sp. ATCC 31554, with predicted amino acid identities varying from 61% to 98%. Both polysaccharides have the same tetrasaccharide repeat unit, comprised of [4)--l-rhamnose-(13)--d-glucose-(14)--d-glucuronic acid-(14)--d-glucose-(1]. Polysaccharide S-88, however, has mannose or rhamnose in the fourth position and has a rhamnosyl side chain, while gellan has no sugar side chain but is modified by glyceryl and acetyl substituents. Genes for synthesis of the precursor dTDP-l-rhamnose were highly conserved. The least conserved genes in this cluster encode putative glycosyl transferases III and IV and a gene of unknown function, gelF. Three genes (gelI, gelM, and gelN) affected the amount and rheology of gellan produced. Four additional genes present in the S-88 sphingan biosynthetic gene cluster did not have homologs in the gene cluster for gellan biosynthesis. Three of these gene homologs, gelR, gelS, and gelG, were found in an operon unlinked to the main gellan biosynthetic gene cluster. In a third region, a gene possibly involved in positive regulation of gellan biosynthesis was identified.     

A simple synthesis of octyl 3,6-di-O-(α-d-mannopyranosyl)-β-d-mannopyranoside and its use as an acceptor for the assay ofN-acetylglucosaminyltransferase-I activity

A simple synthesis of octyl 3,6-di-O-(-d-mannopyranosyl)--d-mannopyranoside is described. The key features of the synthetic scheme are the formation of the -mannosidic linkage by 1-O-alkylation of 2,3,4,6-tetra-O-acetyl-,-d-mannopyranose with octyl iodide and glycosylation of unprotected octyl -d-mannopyranoside using limiting acetobromomannose. The trisaccharide is shown to be an acceptor forN-acetylglucosaminyltransferase-I with aK _M of 585 µm.     

The formation of the mesoderm in urodelean amphibians

Summary Experiments are described in which in early to late blastulae ofAmbystoma mexicanum (stages 7–8/9 Harrison) the animal, ectodermal half (zones I.II) was combined with the vegetative, endodermal yolk mass (zone IV) in various orientations, viz. in random orientation or with the dorso-ventral axes of the two components in identical, opposite or perpendicular orientation (0°, 180°, or 90° translocation respectively). The results demonstrate unequivocally that the dorso-ventral polarity of the induced mesoderm, and thus of the embryo, depends exclusively upon the inherent dorso-ventral polarity of the endoderm, whereas the grey crescent, a considerable part of which is located in the animal, ectodermal half, plays no causal role whatsoever.The results also show that the dorso-ventral polarity is inherent in the entire endodermal mass, but that the subsequent regional differentiation of the endoderm depends upon stimulating influences emanating from the surrounding mesoderm, the later nutritive yolk representing that part of the endoderm which normally does not come under the influence of the mesoderm, and therefore fails to receive the necessary stimulus for further differentiation.On the basis of these findings Schultze's Umkehrexperiment as studied byPenners andSchleip, Penners, andPasteels are reinterpreted, whileDalcq andPasteels' general developmental theory as well asCurtis' cortical grafting experiments are critically discussed.

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Zusammenfassung Es werden Experimente beschrieben, in denen in frühen bis späten Blastulae vonAmbystoma mexicanum (Stadien 7–8/9 Harrison) die animale, ektodermale Hälfte (Zonen I.II) mit der vegetativen, entodermalen Dottermasse (Zone IV) kombiniert wurde, und zwar in verschiedener Orientierung, d. h. in willkürlicher Orientierung oder mit den Dorsoventralachsen der beiden Komponenten identisch, entgegengesetzt oder senkrecht zueinander orientiert (0°, bzw. 180° oder 90° transloziert). Die Ergebnisse zeigen eindeutig, daß die Dorsoventralpolarität des induzierten Mesoderms, und damit die des Embryos, ausschließlich von der inhärenten Dorsoventralpolarität des Entoderms bestimmt wird, während der graue Halbmond, der zu einem beträchtlichen Teil in der animalen, ektodermalen Hälfte liegt, überhaupt keine kausale Rolle spielt.Außerdem zeigen die Ergebnisse, daß die Dorsoventralpolarität der ganzen Entodermmasse inhärent ist, daß aber die spätere regionale Differenzierung des Entoderms von stimulierenden Einflüssen seitens des umgebenden Mesoderms abhängig ist; der spätere Nährdotter ist derjenige Teil des Entoderms der normalerweise außerhalb des Wirkungsbereiches des Mesoderms liegt, und infolgedessen den für seine weitere Differenzierung benötigten Reiz nicht erhält.Angesichts dieser Befunde wird das Schultzesche Umkehrexperiment, welches vonPenners undSchleip, Penners, undPasteels näher untersucht worden ist, neu interpretiert, während die allgemeine Entwicklungstheorie vonDalcq u.Pasteels sowie die Cortextransplantationen vonCurtis kritisch diskutiert werden.

     

Enzymic synthesis of the trisaccharide core region of the carbohydrate chain ofN-glycoprotein

Transmannosylation from mannotriose (Man1-4Man1-4Man) to the 4-position at the nonreducing end N-acetylglucosaminyl residue ofN,N-diacetylchitobiose was regioselectively induced through the use of -d-mannanase fromAspergillus niger. The enzyme formed the trisaccharide Man1-4GlcNAc1-4GlcNAc (3.7% of the enzyme-catalysed net decrease ofN,N-diacetylchitobiose) from mannotriose as a donor andN,N-diacetylchitobiose as an acceptor. Mannobiose (Man1-4Man) was also shown to be useful as a donor substrate for the desired trisaccharide synthesis.Abbreviations Man d-mannose - (M _n) (n=1–5) -linkedn-mer of mannose - GlcNAc₂ 2-acetamido-2-deoxy--d-glucopyranosyl-(1–4)-2-acetamido-2-deoxy-d-glucose     

On anixiopsis stercoraria (hansen) hansen, 1897 and its imperfect stage: Keratinomyces ajelloi vanbreuseghem, 1952

Summary It is herein reported on the discovery of the imperfect stage of an ascomycete,Anixiopsis stercoraria (Hansen)Hansen, 1897, which is also the imperfect stage of another ascomycete,Arthroderma uncinatum,Dawson &Gentles, 1961:Keratinomyces ajelloi Vanbreuseghem, 1952. Thus, the same imperfect form belongs to two different perfect forms.The discovery was made onMicrosporon sp. infected hairs in a case of typical tinea microsporina. The present investigation encompasses 16 strains, all cultured from tinea microsporina. There were both single and double infections.Nine of the cases yieldedAnixiopsis stercoraria along with its imperfect form:Keratinomyces ajelloi Vanbreuseghem, 1952.Four cases revealed a double infection,Keratinomyces ajelloi on one hand and,Arthroderma uncinatum as well asAnixiopsis stercoraria, on the other.The three final cases yieldedM. audouinii andKeratinomyces ajelloi with its perfect form,Anixiopsis stercoraria. K. ajelloi produces only macroconidia, never microconidia. What was mistakenly construed as the microconidia ofK. ajelloi, belongs as microconidia toAnixiopsis stercoraria. Out of these microconidia the development of true macroconidia was observed.Both the relationship of the perfect and imperfect forms ofAnixiopsis stercoraria and cultural characteristics of the perfect form and its pathogenicity are discussed.

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Zusammenfassung Es wird über die Entdeckung der Konidialform eines Ascomyceten berichtet,Anixiopsis stercoraria (Hansen)Hansen, 1897, die zugleich die Konidialform eines anderen Ascomyceten ist,Arthroderma uncinatum,Dawson undGentles, 1961:Keratinomyces ajelloi Vanbreuseghem, 1952. Demzufogle gehört dieselbe Konidialform zwei verschiedenen Ascomyceten an.Die Entdeckung erfolgte an durchMikrosporon infizierten Haaren eines Falles einer klassischen Tinea microsporina. Die gegenwärtige Untersuchung umfasst 16 Fälle, alle von Tinea microsporina der behaarten Kopfhaut herstammend. Die Tinea microsporina war durch einfache und doppelte Infektion verursacht.Neunmal lieferte die KulturAnixiopsis stercoraria zusammen mit der Konidialform:Keratinomyces ajelloi.Viermal lag eine Doppelinfektion vor:Keratinomyces ajelloi, einerseits, undArthroderma uncinatum sowieAnixiopsis stercoraria, andererseits.Endlich lieferten die Kulturen in drei FällenM. audouinii undK. ajelloi zusammen mitAnixiopsis stercoraria. K. ajelloi entwickelt nur Makrokonidia und niemals Mikrokonidia. Was irrtümlicherweise als Mikrokonidia vonK. ajelloi aufgefasst wurde, gehört als MikrokonidiaAnixiopsis stercoraria an. Die Entwicklung von Makrokonidien aus diesen Mikrokonidien wurde beobachtet.Die Wechselbeziehung der Konidial- und Perithecialformen vonAnixiopsis stercoraria, ihr kultureller Charakter und ihre Pathogenität sind einer Diskussion unterzogen.

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Résumé On s'y rapporte à la découverte de la forme conidiale d'un ascomycète,Anixiopsis stercoraria (Hansen)Hansen, 1897, laquelle est, en même temps, la forme conidiale d'un autre ascomycète,Arthroderma uncinatum,Dawson etGentles, 1961:Keratinomyces ajelloi Vanbreuseghem, 1952. Conséquemment, la même forme conidiale appartient aux deux ascomycètes différents.La découverte a été effectuée sur des poils infectés parMicrosporon sp. dans un cas d'une teigne microsporique typique. La présente investigation embrasse 16 cas, provenant tous des cas des teignes microsporiques du cuir chevelu. Des teignes microsporiques ont été causées ou par une simple ou par une double infection.Neuf fois on a obtenu des cultures deAnixiopsis stercoraria avec sa forme conidiale:Keratinomyces ajelloi.Quatre fois il y avait d'infection double:Keratinomyces ajelloi, d'une part, etArthroderma uncinatum etAnixiopsis stercoraria, d'autre part.En fin, les cultures ont démontré en trois cas,M. audouinii etK. ajelloi avecAnixiopsis stercoraria. K. ajelloi ne developpe que des macroconidies et jam ais des micronidies. Ce qu' on avait conçu par erreur comme microconidies deK. ajelloi, appartient comme microconidies à l'Anixiopsis stercoraria. Le développement des macroconidies à partir de ces microconidies a été observé.La relation des formes conidiale et périthéciale del'Anixiopsis stercoraria, son charactère culturel et sa pathogénie ont été discutés.

     

Glycosylation with thioglycosides activated by dimethyl(methylthio)sulfonium tetrafluoroborate: synthesis of two trisaccharide glycosides corresponding to the blood group A and B determinants

Two trisaccharide glycosides,p-trifluoroacetamidophenylethyl 3-O-(2-acetamido-2-deoxy--d-galactopyranosyl)-2-O-(-l-fucopyranosyl)--d-galactopyranoside andp-trifluoroa-cetamidophenylethyl 2-O-(-l-fucopyranosyl)-3-O-(-d-galactopyranosyl)--d-galactopyranoside, corresponding to the human blood group A and B determinants, were synthesized. A key fucosylgalactosyl disaccharide derivative was glycosylated with galactosaminyl or galactosyl donors, respectively. Dimethyl (thiomethyl)sulfonium tetrafluoroborate was used for thioglycoside activation in coupling reactions.     

Nomenklatur,Chromosomenzahlen und Evolution vonArabis auriculata Lam.,A. nova Vill. undA. verna (L.) R.Br. (Brassicaceae)

Zusammenfassung Auf Grund des Holotypus im Herbarium P-LA wird der NameArabia auriculata Lam. als korrekter Name für die am weitesten verbreitete Species der SectionAlomatium DC. emend. O. E.Schulz wieder eingeführt, als deren Typusart sie zugleich vorgeschlagen wird.A. auriculata Lam. 1783 wurde in letzter Zeit fälschlich in europäischen Floren mit dem jüngeren Synonym A. recta Vill. 1789 belegt und in vorderasiatischen Floren A. nova Vill. 1779 genannt.A. nova Vill. ist jedoch eine europäisch-submediterrane Art, die nicht mitA. auriculata Lam. conspecifisch ist. A. auriculata undA. nova sind diploid (2 n=16),A. verna ist tetraploid (2 n=32, diese Zahl wird erstmals veröffentlicht). A. auriculata undA. nova sind vorwiegend autogam,A. verna ist ebenfalls selbstkompatibel und trotz ihrer auffälligeren Blüten fakultativ autogam. Die drei wärmeliebenden Arten sind normalerweise einjährig, manchmal jedoch auch zweijährig. Als Einjährige sind sie in der Gattung als abgeleitet anzusehen.

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Nomenclature, chromosome numbers and evolution ofArabis auriculata Lam.,A. nova Vill., andA. verna (L.) K.Br. (Brassicaceae)

Summary Based on its holotype in the herbarium P-LA the nameArabis auriculata Lam. 1783 is re-established as the correct name of the widespread annual species, which was falsely called A. recta Vill. 1789 in recent European floras, and A. nova Vill. 1779 in recent floras of Western Asia. It is shown that A. nova Vill. refers to a European species of the submediterranean region, which is not conspecific withA. auriculata Lam. A. auriculata Lam. is proposed to be the lectotype ofArabis L. sect.Alomatium DC. emend. O. E.Schulz, comprising the species discussed here. A. auriculata andA. nova are diploids (2 n=16),A. verna is a tetraploid (2 n=32); the latter chromosome number is reported here for the first time. A. auriculata andA. nova are predominantly self-fertilizing,A. verna (though having more conspicuous flowers) is self-compatible and thus facultatively autogamous as well. The three thermophilous species are normally annual, only sometimes biennial. As annuals they are to be regarded as evolutionary derived within the genusArabis.

     

Electrogenic properties of the sodium-alanine cotransporter in pancreatic acinar cells: II. Comparison with transport models

Summary In this paper, the results of the preceding electrophysiological study of sodium-alanine cotransport in pancreatic acinar cells are compared with kinetic models. Two different types of transport mechanisms are considered. In the simultaneous mechanism the cotransporterC forms a ternary complexNCS with Na⁺ and the substrateS; coupled transport of Na⁺ andS involves a conformational transition between statesNCS andNCS with inward- and outward-facing binding sites. In the consecutive (or ping-pong) mechanism, formation of a ternary complex is not required; coupled transport occurs by an alternating sequence of association-dissociation steps and conformational transitions. It is shown that the experimentally observed alanine- and sodium-concentration dependence of transport rates is consistent with the predictions of the simultaneous model, but incompatible with the consecutive mechanism. Assuming that the association-dissociation reactions are not rate-limiting, a number of kinetic parameters of the simultaneous model can be estimated from the experimental results. The equilibrium dissociation constants of Na⁺ and alanine at the extracellular side are determined to beK _N <-64mm andK _S <-18mm. Furthermore, the ratioK _N /K _N ^S of the dissociation constants of Na⁺ from the binary (NC) and the ternary complex (NCS) at the extracellular side is estimated to be <-6. This indicates that the binding sequence of Na⁺ andS to the transporter is not ordered. The current-voltage behavior of the transporter is analyzed in terms of charge translocations associated with the single-reaction steps. The observed voltage-dependence of the half-saturation concentration of sodium is consistent with the assumption that a Na⁺ ion that migrates from the extracellular medium to the binding site has to traverse part of the transmembrane voltage.     

Gene and primary structures of dye-linked <Emphasis Type="SmallCaps">l</Emphasis>-proline dehydrogenase from the hyperthermophilic archaeon<Emphasis Type="Italic"> Thermococcus profundus</Emphasis> show the presence of a novel heterotetrameric amino acid dehydrogenase complex

Dye-linked l-proline dehydrogenase catalyzes the oxidation of l-proline in the presence of artificial electron acceptors such as 2, 6-dichloroindophenol and ferricyanide. The enzyme from the hyperthermophilic archaeon Thermococcus profundus was purified and characterized for the first time in archaea by Sakuraba et al. in 2001. In this study, cloning and sequencing analyses of the gene encoding the enzyme and functional analysis of the subunits were performed. The gene formed an operon that consisted of four genes, pdhA, pdhB, pdhF, and pdhX, which are tandemly arranged in the order of pdhA-F-X-B. SDS-PAGE analysis of the purified recombinant enzyme showed four different bands corresponding to (54 kDa), (43 kDa), (19 kDa), and (8 kDa) subunits encoded by pdhA, pdhB, pdhF, and pdhX, respectively, and the molecular ratio of these subunits was determined to be equal. This indicates that the enzyme consists of a heterotetrameric structure. Functional analysis of each subunit revealed that the subunit catalyzed the dye-linked l-proline dehydrogenase reaction by itself and that, unexpectedly, the subunit exhibited dye-linked NADH dehydrogenase activity. This is the first example showing the existence of a bifunctional dye-linked l-proline/NADH dehydrogenase complex. On the basis of genome analysis, similar gene clusters were observed in the genomes of Pyrococcus horikoshii, Pyrococcus abyssi, Pyrococcus furiosus, and Archaeoglobus fulgidus. These results indicate that the dye-linked l-proline dehydrogenase is a novel type of heterotetrameric amino acid dehydrogenase that might be widely distributed in the hyperthermophilic archaeal strain.Communicated by K. Horikoshi     

Niche,habitat, and related ecological concepts

Summary Darwin's phrase place in natural economy, andSpencer's term correspondence can be regarded as first attempts to express the organism-environment relationships. The same concept has more recently been approached from the point of view of (1) life-form, (2) external activities, and (3) habitat. Though all these points are interlocking, they have been stressed differently in the writings of American and European ecologists. It is proposed that the term niche would be most useful and rational if applied to the total of relationships between a living organism (population, species) and its complete environment, both biotic and abiotic.     

Purification and characterization of an extracellular β-glucosidase from the anaerobic fungus Piromyces sp. strain E2

An extracellular -glucosidase (EC 3.2.2.21) from the anaerobic fungus Piromyces sp. strain E2 was purified. The enzyme is a monomer with a molecular mass of 45 kDa and a pI of 4.15. The enzyme readily hydrolyzes p-nitrophenyl--d-glycoside, p-nitrophenyl--d-fucoside, cellobiose, cellotriose, cellotetraose and cellopentaose but is not active towards Avicel, carboxymethylcellulose, xylan, p-nitrophenyl--d-galactoside and p-nitrophenyl--d-xyloside. To cleave p-nitrophenyl--d-glucoside the maximum activity is reached at pH 6.0 and 55°C, and the enzyme is stable up to 72 h at 40°C. Activity is inhibited by d-glucurono--lactone, cellobiose, sodium dodecyl sulfate, Hg²⁺ and Cu²⁺ cations. With p-nitrophenyl--d-glycoside, p-nitrophenyl--d-fucoside, and. cellobiose as enzyme substrates, the K _m and V _max balues are 1.5 mM and 25.5 IU·mg^-1, 1.1. mM and 133 IU·mg^-1, and 0.05 mM and 55.6 IU·mg^-1, respectively.     

Hexagonally ordered “rosettes” of particles in the plasma membrane ofMicrasterias denticulata Bréb. and their significance for microfibril formation and orientation

Summary Cells ofMicrasterias denticulata Bréb. at the stage of secondary wall formation have been studied by freeze-etching. It was found that the plasma membrane exhibits oval areas in which arrays of membrane particles occur. These particles form rosettes which are arranged in a hexagonally ordered lattice with a center to center spacing of 25 nm. Nearly the same periodicities can be found between microfibrils. It is concluded that the rosettes probably together with the thickened area of the plasma membrane below them represent the apparatus for the production and orientation of microfibrils. The hypothesis suggesting the incorporation of membrane templates functional in microfibril formation, originally advanced byKiermayer andDobberstein (1973) has received further support.     

Purification and biochemical properties of a thermostable xylose-tolerant β-<Emphasis Type="SmallCaps">D</Emphasis>-xylosidase from <Emphasis Type="Italic">Scytalidium thermophilum</Emphasis>

The thermophilic fungus Scytalidium thermophilum produced large amounts of periplasmic -D-xylosidase activity when grown on xylan as carbon source. The presence of glucose in the fresh culture medium drastically reduced the level of -D-xylosidase activity, while cycloheximide prevented induction of the enzyme by xylan. The mycelial -xylosidase induced by xylan was purified using a procedure that included heating at 50°C, ammonium sulfate fractioning (30–75%), and chromatography on Sephadex G-100 and DEAE-Sephadex A-50. The purified -D-xylosidase is a monomer with an estimated molecular mass of 45 kDa (SDS-PAGE) or 38 kDa (gel filtration). The enzyme is a neutral protein (pI 7.1), with a carbohydrate content of 12% and optima of temperature and pH of 60°C and 5.0, respectively. -D-Xylosidase activity is strongly stimulated and protected against heat inactivation by calcium ions. In the absence of substrate, the enzyme is stable for 1 h at 60°C and has half-lives of 11 and 30 min at 65°C in the absence or presence of calcium, respectively. The purified -D-xylosidase hydrolyzed p-nitrophenol--D-xylopyranoside and p-nitrophenol--D-glucopyranoside, exhibiting apparent K_m and V_max values of 1.3 mM, 88 mol min^–1 protein^–1 and 0.5 mM, 20 mol min^–1 protein^–1, respectively. The purified enzyme hydrolyzed xylobiose, xylotriose, and xylotetraose, and is therefore a true -D-xylosidase. Enzyme activity was completely insensitive to xylose, which inhibits most -xylosidases, at concentrations up to 200 mM. Its thermal stability and high xylose tolerance qualify this enzyme for industrial applications. The high tolerance of S. thermophilum -xylosidase to xylose inhibition is a positive characteristic that distinguishes this enzyme from all others described in the literature.