Relationships betweenNor-loci from differentTriticeae species

TheNor-loci of polyploid wheats and their putative diploid progenitor species were assayed by probing isolated nuclear DNA with ribosomal DNA spacer sequences (spacer rDNA sequences, isolated by cloning), from theNor-loci of genomes B (Triticum aestivum), G (T. timopheevi), B (syn. S,T. speltoides), A (T. monococcum) and V (Dasypyrum villosum). DNA samples for analysis were digested with the restriction endonuclease Taq 1 and assayed by DNA-DNA hybridization under standard (37°C) and high stringency (64°C) conditions. The assay procedure emphasized differences between the divergent spacer sequences of the polyploid species and allowed relative homologies to the respective sequences in diploid species to be established. — The studies indicated thatT. timopheevi andT. speltoides contain different sets of spacer rDNA sequences which were readily distinguishable and, in the case ofT. timopheevi, assigned toNor-loci on different chromosomes. This contrast with the spacer rDNA sequences of the majorNor-loci on chromosomes 1 B and 6 B inT. aestivum, which were difficult to distinguish and were deduced to contain very similar sequences. Among the diploid progenitor species only the spacer rDNA fromT. speltoides shared close homology with polyploid wheat species. OneNor-locus inT. timopheevi (on chromosome 6 G) did not show close homology with any of the rDNA spacer probes available. — The data suggestsT. speltoides was the origin of someNor-loci for both theT. timopheevi andT. turgidum lines of tetraploid wheats. The possibility that the 6GNor-locus inT. timopheevi may have derived from an unknown diploid species by introgressive hybridization is discussed. The spacer rDNA sequence probe fromT. monococcum shared good homology with some accessions ofD. villosum and a line ofT. dicoccoides; the implications of this finding for evolution of present-day wheats are discussed.     

Pollen dimorphism in threeTeucrium species (Lamiaceae)

In the Iberian Peninsula and Balearic Islands pollen dimorphism was found inTeucrium fruticans L.,T. pseudochamaepitys L., andT. rotundifolium Schreber. Generally, this dimorphism shows two sizes of pollen grains, the smaller more or less collapsed. The percentage of pollen viability is calculated. Differences in size between viable and nonviable pollen grains are similar, being about 40% inT. fruticans andT. pseudochamaepitys, and about 26% inT. rotundifolium. With regard to pollen viability, the percentage of male sterility is higher inT. fruticans, in which from male sterile (ms) plants, 100% nonviable pollen was obtained from every flower observed. InT. pseudochamaepitys andT. rotundifolium with rare exceptions, the percentage of nonviable pollen does not seem to be significant.     

Some Entolomataceae (Agaricales) from Costa Rica

A preliminary account of Entolomataceae from Costa Rica is presented. Three new taxa are described, two inClitopilus, one inRhodocybe, and three new combinations are proposed inInocephalus. Five taxa ofClitopilus are reported for the first time from Costa Rica and a key to species is provided. Four species ofRhodocybe are discussed and a key to the six species known from Costa Rica is also provided.Alboleptonia earlei, Inocephalus murraii, Inocephalus quadratum, Rhodocybe incarnata andRhodocybe pseudonitellina are now known to occur in Costa Rica.     

New Tigridieae (Iridaceae) from Mexico

A comparison of three heretofore undescribed species with the previously known species inTigridia subgen.Hydrotaenia suggests a realignment of taxa within the various complexes inHydrotaenia. Three species,T. venusta, T. illecebrosa, andT. catarinensis, and two subspecies,T. hallbergii ssp.lloydii andT. ehrenbergii ssp.flaviglandifera, are described.Sessilanthera citrina is described and the new taxonomic combinationS. heliantha (Ravenna) Cruden is proposed.     

Enzyme make-up of trichophyton rubrum and t. mentagrophytes

Summary Aldolase activity in the cell-free extracts of two dermatophytes,T. mentagrophytes andT. rubrum, was investigated. The kinetics of the enzyme and the effects of metal ions and metal-binders are also reported. The enzyme was more active inT. mentagrophytes than inT. rubrum. The optimum pH for the enzyme action was 7.2 and it was completely inactivated at 60° C. Cobalt and magnesium ions and cysteine activated the enzyme. Inhibition caused by EDTA and o-phenanthroline was partially reversed by cobalt ions. The dermatophyte aldolase resembles bacterial aldolase in its properties.     

Effect of diet on the photoperiodic induction of diapause in three species of predatory mite,Amblyseius potentillae,A. cucumeris andTyphlodromus pyri

The predatory mitesAmblyseius potentillae, A. cucumeris andTyphlodromus pyri entered diapause in response to a short-day photoperiodic regime, when they were reared on pollen of the ice plant,Dorotheanthus bellidiformis. With pollen of the broad bean,Vicia faba, as food, however, diapause was virtually absent inA. potentillae andA. cucumeris under the same short-day regime, but full diapause was found inT. pyri. The importance of carotenoids for the photoperiodic response in these predatory mites is discussed.     

Meiotic differences between three triatomine species (Hemiptera,Reduviidae)

We have found the following differences in the male meiosis among three triatomine species: (1) The three largest autosomal bivalents ofTriatoma infestans are heterochromatic.Rhodnius prolixus has two autosomal bivalents with heterochromatic blocks.Triatoma rubrovaria does not show any heteropycnotic autosomes. (2) Sex chromosomes inT. infestans form a chromocenter. At early prophase terminal associations are seen between sex chromosomes inT. rubrovaria, and they maintain a close association until diakinesis. An intimate association between the X and Y chromosomes is observed during early prophase inR. prolixus, but a distant association is maintained by the sex chromosomes at diffuse and diplotene stages in this species. (3) Polyploid nuclei of the nutritive cells are quite distinct. Numerous chromocenters of different shapes and sized are seen in those ofT. infestans. InT. rubrovaria one chromocenter having two positively heteropycnotic elements is observed surrounded by homogeneous chromatin. Only one compact chromocenter is found amongst unevenly distributed chromatin, inR. prolixus.     

Fusarium kyushuense sp. nov. from Japan

Four trichothecene-producing strains originally isolated from diseased wheat and a vinyl plate in Kyushu and Shikoku, Japan are described and illustrated as a new species,Fusarium kyushuense. This species does not produce chalamydospores, which is the key morphological character which distinguishes it fromF. sporotrichioides with which it has been mistaken.Fusarium kyushuense is also differentiated from another morphologically similar species,F. arthrosporioides, by absence of sclerotia and by differences in conidiogenesis of obovate, conidia. InF. arthrosporioides conidia are partly holoblastic from the aerial conidiophores and mostly phialidic from the sporodochial conidiophores, while inF. kyushuense conidia are mostly holoblastic and only produced from aerial conidiophores.     

Malic enzyme,phosphoglucomutase and phosphoglucose isomerase isozymes inTrichogramma [Hym.: Trichogrammatidae]

ME, PGM and PGI electrophoretic banding patterns in 20 laboratory cultures representing 14 species ofTrichogramma were studied. Variations in PGM were found inT. exiguum, T. marylandense, andT. pretiosum. PGI also showed variation inT. exiguum, T. marylandense, T. minutum, andT. parkeri. However, ME variations were found only inT. pretiosum. Based on progeny analyses, we concluded that ME is a tetramer inTrichogramma with fast and slow alleles at a single locus, and that both PGM and PGI have a single locus and each has four alleles. PGM is a monomer, but PGI is a dimer.

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Résumé Les bandes électrophorétiques de l'enzyme malique, de la P.G.M. et de la P.G.I. ont été étudiées chez 20 souches de laboratoire représentant 14 espèces deTrichogramma. Des variations de la P.G.M. ont été trouvées chezT. exiguum, T. marylandense etT. pretiosum. La. P.G.I. montre aussi des variations chezT. exiguum, T. marylandense, T. minutum etT. parkeri. Par contre, des variations de l'enzyme malique ne sont trouvées que chezT. pretiosum. En nous basant, sur l'analyse de progénitures, nous avons conclu que l'enzyme malique est un tétramère chezTrichogramma comprenant un allèle “lent” et un alléle “rapide”, à un seul locus, et que la P.G.M. et la P.G.I. ont chacune un seul locus à quatre allèles. La P.G.M. est un monomère mais la P.G.I. est un dimère.

     

Studies on the phospholipase A of dermatophytes

The presence of phospholipase A activity was detected in three dermatophytes:Microsporum cookei, Trichophyton mentagrophytes, andEpidermophyton floccosum. The activity was always higher inT. mentagrophytes than inM. cookei andE. floccosum. All exhibited phospholipase A₁ and A₂ activities, but the activity was largely A₂ inM. cookei and A₁ inE. floccosum. T. mentagrophytes possessed almost equal activities of phospholipase A₁ and A₂.     

Expression from symbiotic promoters ofRhizobium meliloti inAzotobacter vinelandii andAzospirillum brasilense

InRhizobium meliloti, the promoter P1 of thenif HDK operon, and also the promoter P2, have earlier been shown to be active in the bacteria present in alfalfa root nodules, but not in the bacteria grown aerobically in culture. Here we have looked at the expression from P1 and P2 in two non-symbiotic nitrogen-fixing bacteria,Azotobacter vinelandii andAzospirillum brasilense, using constructions in which the promoters are fused upstream of theβ-galactosidase gene. The promoter P1, but not P2, is active inA. vinelandii, while neither P1 nor P2 is active inAzospirillum brasilense.     

Hybridisation,genomic constitution and generic delimitation inElymus s. l. (Poaceae: Triticeae)

Intergeneric crosses were made between representatives of the genomically-defined generaElymus, Agropyron, Elytrigia, Pseudoroegneria, andThinopyrum. The genomic constitution ofElytrigia repens, the type species ofElytrigia, is shown to be SSH, a genomic combination otherwise found only inElymus. The S genome ofPseudoroegneria has almost always a dominant influence on the morphology of the taxa of which it is a component.Wang (1989) showed that the J genome inThinopyrum and the S genome have considerable homoeology, with a mean c-value of 0.35 in diploid SJ hybrids. A genetic coherence from S to SJ^e, J^e, J^eJ^b, and J^b can be expected, agreeing with the continuous morphologic variation pattern observed. Because of the absence of morphological discontinuities between the taxa,Pseudoroegneria (S),Elymus (SH, SY, sometimes with additional genomes),Elytrigia (SSH, SSHX), andThinopyrum (SJ, SJJ, J) are best treated as a single genus,Elymus, following the generic concept ofMelderis in Flora Europaea and Flora of Turkey. The basic genomic constituents ofElymus will then be the S and/or J genomes.Agropyron, with diploids, tetraploids, and hexaploids based on the P genome is morphologically distinct from other genera inTriticeae. In a few species ofElymus andPseudoroegneria, a P genome is an additional constituent. In these cases the P genome has a negligible morphological influence. Therefore, it seems reasonable to maintainAgropyron as a separate genus.     

Role of genital sex pheromones inAmblyomma americanum andA. maculatum (Acari: Ixodidae)

Amblyomma americanum andA. maculatum were studied to determine if genital sex pheromones were present, as reported inDermacentor species. Chemical analysis of methanol extracts of the anterior reproductive tracts (source of the genital sex pheromone) ofA. americanum andA. maculatum confirmed the presence of the same fatty acids that act as components of the genital sex pheromone inDermacentor variabilis andD. andersoni. In bothAmblyomma species, removal of the anterior reproductive-tract of fed females eliminated the male copulatory response. ForA. americanum, use of anterior reproductive tract extracts made with water, methanol, ether and hexane elicited significant probing and copulatory responses by conspecific males. However, inA. maculatum, use of anterior reproductive-tract extracts made with water, methanol, ether, chloroform: methanol (41), hexane and pentane did not restore mating response by males. Treatment with known components ofDermacentor genital sex pheromones elicited weak but significant responses inA. americanum, but did not restore male mating responses inA. maculatum. These results indicate that genital sex pheromones exist inA. americanum and are not restricted to the genusDermacentor. Characteristics of theAmblyomma genital sex pheromone, however, do differ considerably from those inDermacentor. No genital sex pheromone was present inA. maculatum.     

Sulcal patterns of fossilTheropithecus baboons: Phylogenetic and functional implications

Sulcal patterns were determined from endocasts of fossilTheropithecus (T. oswaldi andT. darti) and compared to the sulcal pattern of extant geladas (T. gelada). A comparison of the configurations of central and arcuate sulci suggests that the cortical motor face representation is relatively enlarged in extantTheropithecus, whereas the cortical motor and sensory face representations were enlarged inT. oswaldi. A relatively expanded sensory and/or motor cortical face representation may be related to masticatory (e.g., “seed-eating”) and gestural (e.g., “lipflip”) functions. SinceT. oswaidi is more derived (expanded) in sensory face representation thanT. gelada, it seems unlikely that it was a direct ancestor of modern geladas. Rather, the two groups were separate by 1.8 million years ago and may have had a most recent common ancestor similar toT. darti from the Hadar Formation of Ethiopia between 2 and 3 million years ago.     

Insertion mutations in the control region of the galactose operon of E. coli. II. Physical characterization of the mutations

Summary Four gal negative mutations, which affect the expression of the gal operon severely as described in the preceding paper (Saedler et al.), are characterized as insertions of DNA by CsCl density gradient centrifugation of transducing phages carrying the mutations and by electron microscopy of hybrid DNA molecules in which the insertion forms a singlestranded loop.Mutation galOP _in 308 is shown by both procedures to be about twice as large as the three other insertions, which are similar in size. The length of the insertions as determined by electron microscopy corresponds to about 1500 nucleotide pairs galOP _in 308 and 800, 700, and 700 nucleotide pairs for galOP _in 128, 141, and 306 respectively. Single-stranded regions are seen in hybrid molecules prepared between DNAs from galOP _in 306 and 128, 141 or 308 as well as from galOP _in 308 and 128. No such single-stranded regions are observed in hybrid molecules between DNAs from galOP _in 128 and 141.Thus, at least three of the four insertions are not identical.     

Toward a High-ResolutionPlasmodium falciparumLinkage Map: Polymorphic Markers from Hundreds of Simple Sequence Repeats

A total of 507 simple sequence repeats (SSRs or “microsatellites”) were identified fromPlasmodium falciparumsequences in GenBank and from inserts in a genomic DNA library. Oligonucleotide primers from sequences that flank 224 of these SSRs were synthesized and used in PCR assays to test for simple sequence length polymorphisms (SSLPs). Of the 224 SSRs, 188 showed SSLPs among 12 differentP. falciparumlines; 116 of these SSLPs were assigned to chromosome linkage groups by physical mapping and by comparing their inheritance patterns against those of restriction fragment length polymorphism markers in a genetic cross (HB3×Dd2). The predominant SSLPs inP. falciparumwere found to contain [TA]_n, [T]_n, and [TAA]_n, a feature that is reminiscent of plant genomes and is consistent with the proposed algal-like origin of malaria parasites. Since such SSLPs are abundant and readily isolated, they are a powerful resource for genetic analysis ofP. falciparum.     

Purification and characterization of glycerate kinase from the thermoacidophilic archaeonThermoplasma acidophilum: An enzyme belonging to the second glycerate kinase family

Thermoplasma acidophilum is a thermoacidophilic archaeon that grows optimally at 59°C and pH 2. Along with another thermoacidophilic archaeon,Sulfolobus solfataricus, it is known to metabolize glucose by the non-phosphorylated Entner-Doudoroff (nED) pathway. In the course of these studies, the specific activities of glyceraldehyde dehydrogenase and glycerate kinase, two enzymes that are involved in the downstream part of the nED pathway, were found to be much higher inT. acidophilum than inS. solfataricus. To characterize glycerate kinase, the enzyme was purified to homogeneity fromT. acidophilum cell extracts. TheN-terminal sequence of the purified enzyme was in exact agreement with that of Ta0453m in the genome database, with the removal of the initiator methionine. Furthermore, the enzyme was a monomer with a molecular weight of 49 kDa and followed Michaelis-Menten kinetics withK _m values of 0.56 and 0.32 mM forDL-glycerate and ATP, respectively. The enzyme also exhibited excellent thermal stability at 70°C. Of the seven sugars and four phosphate donors tested, onlyDL-glycerate and ATP were utilized by glycerate kinase as substrates. In addition, a coupled enzyme assay indicated that 2-phosphoglycerate was produced as a product. When divalent metal ions, such as Mn²⁺, Co²⁺, Ni²⁺, Zn²⁺, Ca²⁺, and Sr²⁺, were substituted for Mg²⁺, the enzyme activities were less than 10% of that obtained in the presence of Mg²⁺. The amino acid sequence ofT. acidophilum glycerate kinase showed no similarity withE. coli glycerate kinases, which belong to the first glycerate kinase family. This is the first report on the biochemical characterization of an enzyme which belongs to a member of the second glycerate kinase family.