Alcuni Aspetti Della Variabilità Del Legno Secondario Di Un Esemplare Di Prunus Persica Stokes

Abstract

Some aspects of the variability in wood structure of a specimen of PRUNUS PERSICA Stokes. — The secondary xylem of a young stem of Prunus persica Stokes has been investigated under three main headings: 1) vessel and fibre length; 2) intrusive fibre growth; 3) relative amount of libriform fibres, fibretracheids and tracheids.

Vessel members and fibres have been reckoned from single rings and from the whole wood body.

The relation between the above mentioned dimensions and the position within the wood body and the width of the growth layers has been calculated.

No remarkable variation has been found along the axis of the stem; on the contrary there is a decrease in both fibres and vessels length along the radius of the stem from inside outwards. Such behaviour having never been recorded before, the possible causes are suggested.

A positive correlation has been found between the width of the growth layers and 1) vessel members and fibres length, 2) fibre intrusive growth, 3) percentage of libriform fibres. In addition a relative correlation between percentage of libriform fibres and age of the cambium has been put in evidence.     

Identification of the allelic state of the <Emphasis Type="Italic">Lr34</Emphasis> leaf rust resistance gene in soft winter wheat cultivars developed in Ukraine

The distribution of alleles at the Lr34 locus associated with leaf rust resistance has been studied in soft winter wheat (Triticum aestivum L.) cultivars developed in Ukraine. To determine the allelic state of the Lr34 locus, codominant molecular marker cssfr5 has been used. Cultivars with the revealed Lr34(+) and Lr34(−) alleles have been identified as potentially resistant or susceptible, respectively. A collection of 81 cultivars from the main breeding centers of Ukraine has been examined; the Lr34(+) allele has been revealed in 44% of the tested cultivars. The obtained results have been compared with general data on the leaf rust resistance of wheat cultivars from different countries.     

Isolation and physical characterization of plasmid pCCl from Corynebacterium callunae and construction of hybrid derivatives

Summary The corynebacteria seem to be the most suitable microorganisms for cloning genes involved in the production of amino acids, nucleotides, and other products of industrial interest. A plasmid, pCCl, from Corynebacterium callunae has been found with a size of 4.3 kb. A physical map obtained with restriction endonucleases is presented. pCCl has single restriction sites for Kpn I, Sma I, Bal I, and Hind III. Copy number of this plasmid has been estimated to be about 30. A number of hybrid plasmids have been constructed between pCCl and pBR329 from Escherichia coli and transformed into corynebacteria. The thiostrepton resistance gene (tsr) from Streptomyces azureus has been inserted into them.     

Ricerche Embriologiche Sul Genere Thalictrum. II. Embriologia e Cariologia Di Thalictrum Lucidum L. e di Thalictrum Minus L. Subsp. Minus

Abstract

Embryological researches in the «Thalictrum» genus. II. Embryology and caryology of «Thalictrum lucidum» L. and «Thalictrum minus» L. ssp. «minus». — In their development the female gametophytes of Thalictrum lucidum L. and Thalictrum minus L. ssp. minus follow the Normal type. In the female gametophytes of these species several types of antipodal cells occurs such as: their considerable enlargement, formation of many antipodals polyploid or polinucleated antipodal cells. In these various types, however, a rapid regression of the antipodals occurs. In T. lucidum some tendency to a disposition of the tetrapolarized type has been verified. The chromosome number has been confirmed to ben 2n=28 in besides, in the pollen development, many cases of regression of the microspores has been verified. The chromosome number has been confirmed to ben 2n=28 in Thalictrum lucidum L., and has been found to ben 2n=14 in Thalictrum minus L. ssp. minus, a new number in this species, which was earlier reported to have 2n=42.     

Genetic studies on theH-3 region of mice and implications for polymorphism of histocompatibility loci

Evidence has been obtained for recombination betweenH-3 and the closely linkedIr-2 locus, which controls the antibody response toEa-1 antigens. The data suggest thatIr-2 maps close toH-3, betweenH-3 andH-13. The YBR strain has been found to possess anH-3 allele not previously reported. A comparison has been made between the degree of polymorphism of histocompatibility loci and that which involves electrophoretically detectable protein variants.     

Biochemical polymorphism in the rat,Rattus norvegicus: Genetic study of four markers

The linkage of the hemoglobin (Hbb) and albino (c) loci has been determined from backcross progeny of the mating (WAG/Orl × Long Evans/Orl)F ₁ × WAG/Orl. The data give 9.1 ± 1.8% recombination. The backcross (August/Orl × WAG/Orl)F ₁ × August/Orl segregating for Hbb and pink-eyed yellow (p) shows 21.5±4.2% recombination. The proposed gene order on linkage group I is p-c-Hbb. Linkage of the seminal vesicle protein (Svp-1) and the nonagouti (a) loci has been determined from backcross progeny of the mating (August/Orl × Long Evans/Orl)F ₁ × Long Evans/Orl. The data show 7.1±3.4% recombination. Svp-1 thus represents an additional marker in linkage group V. Two new autosomal variants have been reported: The locus which controls a plasma protein's polymorphism has been designated Gl-1 with two codominant alleles Gl-1a and Gl-1b. The other locus, controlling a testis esterases polymorphism, has been assigned the symbol Es-3 and has two codominant alleles Es-3a and Es-3b. The absence of linkage of Gl-1 and Es-3 to each other and to five different loci has also been reported. Rat and mouse analogy with respect to these markers and established linkages is discussed.     

Genetics and physiology of the rel system of Bacillus subtilis

Summary Stringent factor (ATP:GTP-3 pyrophosphotransferase) has been purified from wild type Bacillus subtilis and it has been shown that guanosine tetra- and pentaphosphate (ppGpp and pppGpp) are synthesized in vitro in the presence of ribosomes, unacylated tRNA and its specific codon, as has been demonstrated in Escherichia coli. relA, the genetic determinant for the stringent factor, has been mapped on the B. subtilis chromosome by transduction and is found between aroD and leu.The relC locus, defined by mutations which were originally selected by resistance to thiostrepton, has been mapped adjacent to spoOH in the order cysA, spoOH, relC, rif.Stringent factor and ribosomes are functional for the in vitro synthesis of (p)ppGpp in early stages of sporulation (up to at least 4 h). This contradicts the findings of other laboratories.     

The terminal oxidases of Paracoccus denitrificans

Three distinct types of terminal oxidases participate in the aerobic respiratory pathways of Paracoccus denitrificans. Two alternative genes encoding sub unit I of the aa₃-type cytochrome c oxidase have been isolated before, namely ctaDI and ctaDII. Each of these genes can be expressed separately to complement a double mutant (ActaDI, ActaDII), indicating that they are isoforms of subunit I of the aa₃-type oxidase. The genomic locus of a quinol oxidase has been isolated: cyoABC. Thisprotohaem-containing oxidase, called cytochrome bb₃, is the oniy quinoi oxidase expressed under the conditions used, in a triple oxidase mutant (ActaDI, ActaDII, cyoB::Km^R) an alternative cyto-chrome c oxidase has been characterized; this cbb₃-type oxidase has been partially purified. Both cytochrome aa₃ and cytochrome bb₃ are redox-driven proton pumps. The proton-pumping capacity of cytochrome cbb₃ has been analysed; arguments for and against the active transport of protons by this novel oxidase complex are discussed.     

Taxonomic studies of Choanephoraceae in India

Summary A taxonomic study of the members of the family Choanephoraceae was undertaken. Almost all the species of the family have been isolated from various sources in India. Two genera, viz.,Blakeslea andChoanephora have been recognized and a key to the genera has been given. The genusBlakeslea includes only one speciesB. trispora and the genusChoanephora five species. A key to the species has also been given. A new variety ofChoanephora circinans, viz.,C. circinans var.prolifera Mehrotra andMehrotra based on the proliferating vesicular apices of the sporangiophores has been described.     

Genetic control of two electrophoretic variants of glucosephosphate isomerase in the mouse (Mus musculus)

The autosomal variation and the genetic control of GPI has been determined by a comparison of electrophoretic patterns of F₁ and backcross progeny of three inbred strains of mice. The locus controlling the production of GPI in the mouse has been designated Gpi-1. Two alleles at this locus have been described and designated Gpi-1 ^a and Gpi-1 ^b, which represent, respectively, the slow and fast electrophoretic forms. Twenty-seven inbred strains of mice have been classified for these two alleles. The absence of close linkage of Gpi-1 to seven other genetic loci has been determined. It has been demonstrated that the polymorphism of Gpi-1 is widely distributed in feral mice. GPI was expressed in vitro and in four types of malignant tumors.Supported by U.S. Public Health Service Grants GM-09966, from General Medical Sciences, and GY 4193.     

Studies in aquatic fungi of Varanasi IV. new records and notes on taxonomy

Summary In continuation with the studies in aquatic fungi of Varanasi, four more fungi viz., Achlya apiculata, A. oblongata var. oblongata, Blastocladiella simplex and Pythiogeton ramosum have been isolated and described as occurring new to the Indian aquatic flora; while P. sterilis has been assigned to synonymy under P. ramosum Hamid's isolate A. oblongata var. oblongata has been excluded from the valid identification.     

Premeiotic disruption of the Neurospora crassa malate synthase gene by native and divergent DNAs

Summary Repeat-induced point mutation (RIP) has been used to generate new mutations in the previously uncharacterised gene for malate synthase in Neurospora crassa. Molecular clones carrying the am (NADP-glutamate dehydrogenase) gene and the malate synthase gene from either N. crassa or Aspergillus nidulans have been introduced into Neurospora as ectopic duplicate copies by transformation, selecting for the am function in a deletion host. A number of meiotic progeny derived from these transformants were unable to use acetate as sole carbon source, yielded no detectable malate synthase activity and demonstrated extensive cytosine methylation of their duplicated sequences. The new locus has been designated acu-9 and has been assigned to linkage group VII.     

The expression of genes encoding the voltage-dependent L-type Ca<Superscript>2+</Superscript> channels in proliferating and differentiating C2C12 myoblasts of mice

Voltage-dependent L-type Ca⁺ channels of the C2C12 line myoblasts of mice have been studied at the stage of proliferation and 24 h after the beginning of differentiation. The expression of genesCacna1s, Cacna1c, Cacna1d, and Cacna1f, which encode channel forming subunits α₁S, α₁C, α₁D, and α₁F, respectively, has been assessed. The expression of genes Cacna2d and Cacn1g, which encode the α₂, δ, and γ regulatory subunits, has been studied as well. For the first time, the expression of Cacna1d, which is typical for nerve cells, has been revealed in proliferating myoblasts, whereas in differentiating mononuclear myoblasts the expression of this gene was significantly decreased. On the contrary, the low level of expression of Cacna1S, which encodes the specific α1S channel forming subunit of skeletal muscles, has been observed in proliferating myoblasts, whereas in differentiating mononuclear myoblasts it has been shown to increase multifold. No considerable changes in expression of Cacna2d and Cacn1g have been revealed in proliferating and differentiating myoblasts. No traces of expression of Cacna1c and Cacna1f have been revealed in myoblasts.     

Pteromalidae etEulophidae nouveaux d'Europe (Hym., Chalcidoidea)

Summary In the present paper the Author has described three new genera ofPteromalidae, two new species of the genusEnaysma Del. and one of the genusEpilampsis Del. (Euloph. Entedontinae). The first Pteromalid genus,Stenoselma, is closely related to the well knownAnisopteromalus Ruschka; the second new genus,Apelioma, has been proposed forDinotiscus (Dinotus) pteromalinus Thomson; the third,Aggelma, has been described for the new speciesabdominalis, collected in Central Europe onPinus montana. The other new species ofEntedontinae has been bred from leaf-miners (Lepidoptera).      

Endophytic fungal entomopathogens with activity against plant pathogens: ecology and evolution

Dual biological control, of both insect pests and plant pathogens, has been reported for the fungal entomopathogens, Beauveria bassiana (Bals.-Criv.) Vuill. (Ascomycota: Hypocreales) and Lecanicillium spp. (Ascomycota: Hypocreales). However, the primary mechanisms of plant disease suppression are different for these fungi. Beauveria spp. produce an array of bioactive metabolites, and have been reported to limit growth of fungal plant pathogens in vitro. In plant assays, B. bassiana has been reported to reduce diseases caused by soilborne plant pathogens, such as Pythium, Rhizoctonia, and Fusarium. Evidence has accumulated that B. bassiana can endophytically colonize a wide array of plant species, both monocots and dicots. B. bassiana also induced systemic resistance when endophytically colonized cotton seedlings were challenged with a bacterial plant pathogen on foliage. Species of Lecanicillium are known to reduce disease caused by powdery mildew as well as various rust fungi. Endophytic colonization has been reported for Lecanicillium spp., and it has been suggested that induced systemic resistance may be active against powdery mildew. However, mycoparasitism is the primary mechanism employed by Lecanicillium spp. against plant pathogens. Comparisons of Beauveria and Lecanicillium are made with Trichoderma, a fungus used for biological control of plant pathogens and insects. For T. harzianum Rifai (Ascomycota: Hypocreales), it has been shown that some fungal traits that are important for insect pathogenicity are also involved in biocontrol of phytopathogens.     

The plastid rpoA gene encoding a protein homologous to the bacterial RNA polymerase alpha subunit is expressed in pea chloroplasts

Summary The gene rpoA, encoding a protein homologous to the alpha subunit of RNA polymerase from Escherichia coli has been located in pea chloroplast DNA downstream of the petD gene for subunit IV of the cytochrome b-f complex. Nucleotide sequence analysis has revealed that rpoA encodes a polypeptide of 334 amino acid residues with a molecular weight of 38916. Northern blot analysis has shown that rpoA is co-transcribed with the gene for ribosomal protein S11. A lacZ-rpoA gene-fusion has been constructed and expressed in E. coli. Antibodies raised against the fusion protein have been employed to demonstrate the synthesis of the rpoA gene product in isolated pea chloroplasts. Western blot analysis using these antibodies and antibodies against the RNA polymerase core enzyme from the cyanobacterium, Anabaena 7120, has revealed the presence of the gene product in a crude RNA polymerase preparation from pea chloroplasts.     

Nucleotide sequence of Citrus limon 26S rRNA gene and secondary structure model of its RNA

The complete nucleotide sequence of Citrus limon 26S rDNA has been determined. The sequence has been aligned with large ribosomal RNA (L-rRNA) sequences of Escherichia coli, Saccharomyces cerevisiae and Oryza sativa. Nine extensive expansion segments in dicot 26S rRNA relative to E. coli 23S rRNA have been identified and compared with analogous segments of monocot, yeast, amphibian and human L-rRNAs. A secondary structure model for lemon 26S rRNA has been derived based on the refined model of E. coli 23S rRNA. It has been compared with other eukaryotic L-rRNAs models in terms of location of functionally important regions. Origin and evolution of L-rRNA expansion segments are discussed.     

Kinetics of batch-wise enzymatic cycling system for mass production of chiral compound

Kinetics of batch-wise enzymatic cycling system (oxidoreductase-catalyzed reaction system involving enzyme-coupled cofactor regeneration) has been studied covering a broad range of the conserved total cofactor concentration, [C]₀ (=NAD(P)⁺?+?NAD(P)H), based on reasonable several assumptions. It is composed of two elementary reactions, i.e. product synthesis reaction and cofactor regeneration reaction, both of which have been expressed by Michaelis–Menten type rate equations. A novel dimensionless variable, r, has been introduced, which is defined as the concentration of one of the two cofactor components, [X] (NADH⁺ or NADPH⁺), divided by [C]₀, i.e. r .e[X]/[C]₀. The following results have been obtained. (1) The fundamental equation of the batch-wise enzymatic cycling system has been transformed to a differential equation whose formula is: dr/dT?=?N(r)/D(r) (N(r) and D(r) are quadratic equations of r having different coefficients). (2) It has been elucidated that the batch-wise enzymatic cycling system has two phases, an early short transient phase followed by a long phase in quasi-steady state (QSS). (3) In the enzymatic cycling system, r converges to a definite level regardless of any initial value of r. (4) In QSS, the definite level of r nearly equals the singular solution, r_singular, of the differential equation. (5) The actual rate of the targeted product (chiral compound) formation can be calculated by Michaelis–Menten equation in which the cofactor concentration is [C]₀×r_singular instead of [C]₀. r_singular has been proposed to name “redistribution factor”. (6) It is recommended that the “unit” of the cofactor regeneration enzyme be 2–3 times more used than the “unit” of the synthesis enzyme and that [C]₀ be 15–25 times more than the K_m value. Four special cases relating to the batch-wise enzymatic cycling system have been discussed.     

Fouling Communities of Hydrotechnical Constructions in Nakhodka Bay (Sea of Japan)

The fouling of mooring facilities in Nakhodka Bay, Sea of Japan, has been studied. The main fouling communities have been distinguished dominated by green algae Enteromorpha linza and Ulva fenestrata, brown algae Laminaria japonica and Costaria costata, a hydroid Obelia longissima, a polychaete Pseudopotamilla occelata, cirripede barnacles Balanus crenatus and Semibalanus cariosus, a bivalve mollusk Mytilus trossulus, and an ascidian Halocynthia aurantium. The naturalization of some species-invaders in the fouling of mooring facilities in Nakhodka Bay has been registered, namely hydroids Laomedea flexuosa and Clytia languida, a polychaete Pseudopotamilla occelata, and a bryozoan Bowerbankia gracilis.