Chemotaxonomy of the genus Talaromyces

Species of the ascomycetous genus Talaromyces have been examined for profiles of secondary metabolites on TLC. The greatest number of specific metabolites were produced on oatmeal-, malt extract- and yeast-extract sucrose agars. Profiles of intracellular secondary metabolites produced on oatmeal agar were specific for each species and provided a means of simple differentiation of the taxa. Examination of the most important species using high performence liquid chromatography (HPLC) allowed to solve some taxonomic problems. Known mycotoxins are produced by T. stipitatus (duclauxin, talaromycins, botryodiploidin), T. stipitatus chemotype II (emodin), T. panasenkoi (spiculisporic acid), T. trachyspermus (spiculisporic acid), T. trac macrosporus (duclauxin) and T. wortmannii (rugulosin). Wortmannin is produced by an atypical strain of T. flavus but not T. wortmannii. Several other secondary metabolites were discovered for the first time in the following species: Glauconic acid is produced by T. panasenkoi, T. ohiensis and T. trachyspermus; vermiculine by T. ohiensis; duclauxin by T. flavus var. macrosporus and the mitorubrins by T. flavus and T. udagawae. The profiles of secondary metabolites support the established taxonomy of the species based on morphology, showing the genetic stability of profiles of secondary metabolites in Talaromyces. Two new taxa are proposed: T. macrosporus comb. nov. (stat. anam. Penicillium macrosporum stat. nov.), and Penicillium vonarxii, sp. nov. for the anamorph of T. luteus.     

Alteration of cell surface carbohydrates associated with ordered and disordered proliferation of oral epithelia: a lectin histochemical study in oral leukoplakias, papillomas and carcinomas

Cell surface carbohydrates in healthy oral mucosa (n = 15), leukoplakias without (n = 48) and with (n = 62) dysplasia, oral papillomas (n = 6) and squamous cell carcinomas (SCCs) (n = 40) were examined using the lectins peanut agglutinin (PNA), Ulex europaeus agglutinin I (UEA I), soybean agglutinin (SBA), Helix pomatia agglutinin (HPA), and Griffonia simplicifolia agglutinin I (GS I-B4). Binding of these lectins in formalin-fixed, paraffin-embedded tissues was demonstrated using either the peroxidase-anti-peroxidase (PAP) method or the avidin-biotin method. Healthy oral epithelia revealed binding sites for these lectins mostly in the suprabasal keratinocytes with occasional PNA binding also in their basal cells. Unlike healthy mucosa, a number of leukoplakias without and with dysplasia revealed receptor sites for UEA I also in their basal layer. Only those keratinocytes undergoing squamoidal differentiation exhibited SBA binding. Staining patterns of UEA I and SBA did not vary significantly between either leukoplakias without and with dysplasia or papillomas and SCCs. Conversely, a reduction or lack of binding sites for PNA (Gal beta 1-3GalNAc), HPA (D-GalNAc alpha) and GS I-B4 (alpha D-Gal) was observed more frequently in leukoplakias with dysplasia and SCCs contrasting their counterparts lacking epithelial dysplasia. Cell surface glycosyl residues play an important role in the regulation of cell proliferation and epithelial growth. Aberrant glycosylation in oral dysplastic leukoplakias and carcinomas leading to the lack of the relevant terminal sugar residues from their cell surface carbohydrates is probably a major reason for the hyper-/disordered proliferation.     

Response analysis of vertebrate retina

In a recent work (Ouztöreli, 1980) a mathematical model for studying the neural activities in a vertebrate retina has been investigated, where the basic network contains five interconnected neurons: a receptor cell, a bipolar cell, a horizontal cell, an amacrine cell, and a retinal ganglion cell. More recently, in (Ouztöreli and O'Mara, 1980) the basic network has been extended to a larger network containing twelve neurons. In both of these works, the performances of the basic and extended models were discussed under different structural and processing conditions with constant inputs by using the results of one of our earlier work (Ouztöreli, 1979). In the present paper we investigate by simulations the responses of the basic retinal network to piecewise constant and periodic inputs. The step and frequency responses of the extended retinal network will be discussed in a forthcoming paper.This work was partially supported by the Natural Sciences and Engineering Research Council of Canada under Grant A-4345 through the University of alberta     

The Roberts syndrome

Summary Four siblings with the autosomal recessive Roberts syndrome are reported, and we discuss the phenotypic overlap of this syndrome with other similar radial, aplasia syndromes.     

Stereological Analysis of Floral Development and Quantitative Histochemistry of Nucleic Acids in Fertile and Base-sterile Varieties of Wheat

The speltoid series of mutations provides a genetic tool forinvestigating the control of flower development. In fertileGabo wheat and in St₂ and St₃ basal sterile speltoids, the changesin RNA staining patterns have been followed histochemicallyas a marker of cellular activity. Sterile floret sites are characterizedby a reduced RNA content. Use of dual-wavelength microspectrophotometryhas provided evidence that RNA content is similar in lemma primordiasubtending presumptive fertile and sterile primordia, but isstrikingly different in the floral meristems in the two types.The total nucleic acid content of the floral primordia has beenrelated to the number of epidermal cells in the subtending lemmaprimordium as a marker of development, using a linear modelanalysis of covariance. There is a linear increase in nucleicacid content during fertile floret development, but no significantincrease in RNA content in sterile St₃ primordia. The rate constantis only 1/10th to 1/20th of that of Gabo. A stereological analysisshows that cell number in the floral meristems of Gabo increasesexponentially during development. In contrast, in St₃, whilethere is a significant increase in cell number, it is at a drasticallyreduced rate. The intercept values are close to zero, indicatingthat only one or two cells initiate floral meristem development.The fertility-controlling alleles exert their effect prior tothe appearance of a visible floral primordium, and probablyafter initiation of the lemma. Triticum aestivum, wheat, floral development, histochemistry, nucleic acids, speltoids     

Plasmids of serogroup 1 strains ofLegionella pneumophila

Twelve strains ofLegionella pneumophila were tested for the presence of plasmid DNA. Three strains, belonging to serogroup 1, had large plasmids of 83.8×10⁶ daltons, as determined by electron microscopy. A fourth strain, also from serogroup 1, had a similar large plasmid in addition to a smaller plasmid. Restriction analysis of plasmid DNA isolated from the strains with a single size plasmid indicated that the plasmids were structurally very similar. The biologic functions of these plasmids are yet to be determined.     

Substance P inhibition of the activity of the angiotensin-converting enzyme from human blood serum

Substance "P" (SP) and its derivatives inhibited activity of angiotensin-converting enzyme (ACE) in human blood serum, I50 for SP was 31 microM. The same results were obtained for N-terminal fragments of the SP molecule: Arg-Pro-Lys-Pro and Lys-Pro. The C-terminal heptapeptide and the dipeptide Arg-Pro negligibly inhibited ACE activity. A possible significance of the interaction between SP and ACE in the regulation of the microhemodynamics is discussed.     

Experience with the international standardization of the biological activity of the 3d Standard for streptomycin

The activity of the third International Standard of streptomycin was determined to be equal to 755 IU/mg with the use of accurately weighed amounts of streptomycin and 78037 IU with the use of streptomycin ampoules. The Standardization Center of the WHO decided to use the whole content of the ampoule of the Third International Standard of streptomycin, the activity of which is determined to be equal to 78500 IU per an ampoule.     

Thermal history of reef-associated environments during a record cold-air outbreak event

Summary Several polar continental air masses intruding into the south Florida/northern Bahama Bank region during January 1981 caused record low air temperatures and rapid chilling of extensive shallow-water carbonate systems. Numerous coral kills along the Florida reef tract and massive fish mortalities in Florida Bay were attributable to unusually cold waters generated at this time. Thermal evolution of Florida Bay/Florida reef tract and northern Bahama Bank waters from 8 to 21 January was assessed from thermal infrared data acquired by the NOAA-6 environmental satellite, in situ water temperatures, local meteorological data, and a computerized heat flux model. Field observations and laboratory experiments identify 16°C as a thermal stress threshold for most reef corals (Mayor 1915; Davis 1981). Temperaturecorrected digital satellite data indicated that water temperatures below 16°C were generated in Florida Bay and on Little and Great Bahama Banks during a 10-day period in January. Lowest temperatures on the Florida reef tract resulted from offshelf transport of Florida Bay water through major tidal channels. Offshelf movement of bay water is driven primarily by strong northerly winds, density gradients, and tidal pumping. Absence of reef development opposite major tidal passes along the Florida reef tract (Ginsburg and Shinn 1964) and aperiodic coral kills along bank margins can be attributed to this process, which has probably had a limiting influence on Holocene reef development in these areas.