Development of telial head in Ravenelia species

Development and cytology of the telial head in Ravenelia sessilis Berkeley, R. taslimii Mundkurs and R. ornata Sydow are traced in the ontogenic sequence. The species parasitic on leguminous hosts show some variations among themselves in the development of the telial heads and from those parasitizing euphorbiaceous hosts.     

Ravenelia cenostigmatis, a new rust fungus from Brazil

Ravenelia cenostigmatis is described as a new species of plant rust (Uredinales) onCenostigma gardnerianum (Caesalpiniaceae) from Brazilian Cerrado. Teliospore heads ofR. cenostigmatis exhibit an unusually complex structure with four different kinds of cells: teliospore cells, sterile apical cells (intercalary between pedicel hyphae and teliospores), sterile hygroscopic cysts, and morphologically distinct border cells. The last are flattened, elaborately ornamented and probably sterile cells that are wedged between the teliospores and the cysts.Ravenelia cenostigmatis probably belongs to a natural assemblage of ravenelias that occur on caesalpiniaceous hosts and exhibit similar morphological traits. Part 179 of the series “Studies in Heterobasidiomycetous Fungi” of the Botanical Institute, University of Tübingen     

Development and parasitism in the genus Hemileia (uredinales)

Seventeen species ofHemileia were studied with emphasis on these characters: extent of colonization, specialization of parasitic mycelium, haustorial development, pathologic histology, soral morphology and sporulation capacity. An attempt was made to trace the varying degree of development and parasitism in this rust genus comprising of just over 40 reported species. It was noted that theGopalkrishnan's Subepidermal type more advanced than his Superstomal — B type.Fourth part of my thesis submitted to the University of Poona, India, accepted in 1968 for Ph.D. Not published.     

Development of expressed sequence tag derived-simple sequence repeats in the genus Lilium

Although lily is the second largest flower crop in cutting flower commodity, only six simple sequence repeats SSRs have been reported. Thus, we developed expressed sequence tag derived-SSRs (EST-SSRs) for the Lilium genus. Among 2,235 unique ESTs, 754 ESTs contained SSR motifs, among which 165 ESTs were amenable to primer design. Among these 165 EST-SSRs, 131 EST-SSRs showed amplification in at least one Lilium species, and 76 EST-SSRs showed amplification in at least nine species. Of the 76 EST-SSRs, 47 showed amplification in all Lilium species analyzed. Using 10 breeding lines, we selected 21 EST-SSRs that had the highest number of alleles and polymorphism information content. The polymorphism information content values of these selected EST-SSRs ranged from 0.49 to 0.94 with an average of 0.76, which are higher than other plant species. The phylogenetic dendrogram derived from the amplification profiles of the 21 high polymorphic EST-SSRs was congruent with the genetic background of the 84 selected lily accessions and hybrids, which are available in commerce. Thus, the developed EST-SSRs will be very useful in germplasm management, genetic diversity analysis, cultivar finger printing, and molecular breeding in the lily.     

Development rate of copepod eggs of the genus Calanus

The development time to hatching of eggs of four closely related species of copepods, Calanus helgolandicus (Claus), C. finmarchicus (Gunn.), C. glacialis Jaschnov, and C. hyperboreus Kröyer as a function of temperature is given by .

The constant a is positively correlated with egg diameter, so that large eggs take longer to develop than small eggs. The value of the constant is related to the geographical range of the species.     

Development of SSR markers to study diversity in the genus Cymbidium

Cymbidium spp. are important potted flowers with extremely high ornamental and economic value. The present study reports the development of 14 new simple sequence repeat (SSR) markers through the construction of an enriched Cymbidium goeringii library and cross-amplification in Cymbidium sinensis and Cymbidium hybridium. Of 525, 322 (61.33%) clones had SSR motifs and among motifs di-nucleotides were predominant and followed by tri-nucleotide and tetra-nucleotide type. In polymorphic analysis using 14 newly developed SSRs, a total of 201 alleles across 96 Cymbidium accessions were detected with an average of 14.4 per locus. The average heterozygosity was 0.394. The average gene diversity and polymorphism information content values were 0.394 and 0.639, respectively. The mean genetic similarity coefficient was 0.4297, indicating a wide genetic variation among the Cymbidium accessions. These newly developed SSRs will be useful tools for genotype identification, germplasm conservation, molecular breeding, and assessments of genetic diversity and population structure in Cymbidium.     

Development and characterization of monoclonal antibodies specific for the genus Listeria

Abstract Monoclonal antibodies were obtained by the classic hybridoma technique with lymphocytes of BALB/c mice immunized with formalin killed Listeria monocytogenes cells. Among 1000 hybridomas issued from the fusion, four monoclonal antibodies (mAbs A6 A E4, C10 A F7, G4 A D6, G7 A D5) gave interesting results. By Western-blot analysis with various soluble extracts of different Listeria species, the four mAbs reacted with two major antigens of 38 and 41 kDa, with all Listeria species tested. The mAb A6 A E4 is an IgG2b with κ light chains and reacted only with Listeria antigens without any cross reaction with other organisms tested by ELISA, dot-blotting and Western-blotting. With the same conditions, the three other mAbs reacted with Listeria and with other genus extracts, particularly with Streptococcus and Enterococcus . mAb A6 A E4-reactive antigens are proteins, and glycoprotein immunoassay indicated that the epitope is devoid of carbohydrate moiety. This mAb A6 A E4-reactive protein was neither expressed on cell surface nor released outside the bacteria; immunogold electron microscopy showed that these antigens were localized in the cytoplasma area.     

Development of a new chemically defined sporulation medium for the yeasts in the genus Lipomyces

A chemically defined sporulation medium (AF medium) for the yeasts belonging to the genus Lipomyces was developed. The chemical composition was derived from chemical analyses of soybean extract. Some chemical modification of the AF medium indicated that the nitrogen sources (aspartic and glutamic acids) and zinc ion were essential for sporulation. The significance of medium pH was discussed.     

Development of a nutrient medium to culture microorganisms of the genus Campylobacter

The nutrient media developed in the USSR and CSR for the isolation of campylobacteria are multi-purpose as they enable the isolation of campylobacteria not only from material derived from patients with acute intestinal infection, but also from the internal organs of healthy and diseased animals and poultry as well as from a variety of objects in the environment.     

Development of a recA gene-based identification approach for the entire Burkholderia genus

Burkholderia is an important bacterial genus containing species of ecological, biotechnological, and pathogenic interest. With their taxonomy undergoing constant revision and the phenotypic similarity of several species, correct identification of Burkholderia is difficult. A genetic scheme based on the recA gene has greatly enhanced the identification of Burkholderia cepacia complex species. However, the PCR developed for the latter approach was limited by its specificity for the complex. By alignment of existing and novel Burkholderia recA sequences, we designed new PCR primers and evaluated their specificity by testing a representative panel of Burkholderia strains. PCR followed by restriction fragment length polymorphism analysis of an 869-bp portion of the Burkholderia recA gene was not sufficiently discriminatory. Nucleotide sequencing followed by phylogenetic analysis of this recA fragment differentiated both putative and known Burkholderia species and all members of the B. cepacia complex. In addition, it enabled the design of a Burkholderia genus-specific recA PCR that produced a 385-bp amplicon, the sequence of which was also able to discriminate all species examined. Phylogenetic analysis of 188 novel recA genes enabled clarification of the taxonomic position of several important Burkholderia strains and revealed the presence of four novel B. cepacia complex recA lineages. Although the recA phylogeny could not be used as a means to differentiate B. cepacia complex strains recovered from clinical infection versus the natural environment, it did facilitate the identification of clonal strain types of B. cepacia, B. stabilis, and B. ambifaria capable of residing in both niches.     

Ravenelia species (Pucciniales) newly found in Thailand with their additional host and life cycle stage

Three poorly known species of Ravenelia with limited geographic distribution and one widespread species parasitizing leguminous trees (Fabaceae) were newly found in Thailand. Ravenelia odoratissimae occurred on Albizia odoratissima; R. ornata on Abrus pulchellus, Ab. precatorius, and Abrus sp.; R. parasnathii on Acacia comosa and an unidentified Acacia species; and R. tandonii on Acacia catechu. Acacia comosa is a new host for R. parasnathii. Detailed morphological study revealed that R. odoratissimae produces a uredinial stage in addition to a telial stage in its life cycle.