Karyotype and meiosis studies in three South African Pyrgomorpha species (Orthoptera: Pyrgomorphidae)

Two South African Pyrgomorpha species have reduced chromosome numbers, due to centric fusions between the largest autosomes and the medium and small autosomes. P. rugosa has 2n=11(XO) (4 pairs of submetacentric and 1 pair of acrocentric autosomes) and P. granulata has 2n=13(XO) (3 pairs of submetacentric and 3 pairs of acrocentric autosomes). A third South African species has a typical Pyrgomorphidae number of 2n=19(XO) (acrocentrics). The mean chiasma frequency of the 2n=19 species is higher than that of the other two, although the frequencies of distal chiasmata in all three are similar. The recombination potential of the two species with lower chromosome numbers has been reduced, due to fewer crossovers in comparison to the 2n=19 species, as well as to independent assortment.     

Properties of a pentulose-5-phosphate phosphoketolase from yeasts grown on xylose

Summary Phosphoketolase activity from nine yeasts grown on xylose occurred with both xylulose 5-phosphate (Xu5P) and ribulose 5-phosphate (Ru5P) as substrates. With extracts from five yeasts (Candida curvata, C. famata, Lipomyces starkeyi, Rhodotorula glutinis and Pachysolen tannophilus) activity was approximately the same with either substrate; with C. boidinii, Pichia media and Yarrowia lipolytica Ru5P was the preferred substrate; and with Rhodosporidium toruloides Xu5P was the better substrate. Partial purification of the phosphoketolase from C. famata was attempted: although activity of phosphoketolase towards Ru5P was decreased it was not eliminated and it is concluded that either (i) the phosphoketolase does have dual substrate specificity, in which case it should be referred to as a pentulose-5-phosphate phosphoketolase (Pu5PPK) or (ii) Ru5P-3-epimerase activity, which can interconvert Xu5P and Ru5P, may be closely associated with phosphoketolase activity. The Pu5PPK has a of 2.4mm for Xu5P, a pH optimum of 7.2–7.4 and a M _r of 5x10⁵ daltons. It is not sensitive to inhibition by citrate or acetyl-CoA at physiological concentrations.     

Biochemical evidence for the histochemical localization of linamarase activity inLotus corniculatus infected withStemphylium loti

Summary -glucosidases in healthy trefoil, inStemphylium loti, and inS. loti-infected trefoil have been purified and identified as linamarases byin vitro assays. The location of -glucosidase activity in these same organisms was determined histochemically by modification of a simultaneous coupling azo-dye technique using bromonaphthyl glucoside as a substrate. The histochemical method was adapted for a quantitative spectrophotometric determination ofin vitro enzyme activity on this substrate. Each purified -glucosidase was activein vitro on linamarin and the histochemical substrate. With concurrent biochemical and histochemical analyses, it was shown that the localized -glucosidases were linamarases. Linamarase activityin situ was localized in the phloem, epidermis, and mesophyll in healthy and in infected trefoil leaves and inS. loti hyphae growing either on the surface or in infected tissue.     

Pentose utilization and transport by the ruminal bacterium Prevotella ruminicola

Plant cell wall polysaccharides are primarily composed of hexose or hexose derivatives, but a significant fraction is hemicellulose which contains pentose sugars. Prevotella ruminicola B₁4, a predominant ruminal bacterium, simultaneously metabolized pentoses and glucose or maltose, but the organism preferentially fermented pentoses over cellobiose and preferred xylose to sucrose. Xylose and arabinose transport at either low (2 M) or high (1 mM) substrate concentrations were observed only in the presence of sodium and if oxygen was excluded during the harvest and assay procedures. An artificial electrical potential () or chemical gradient of sodium (pNa) drove transport in anaerobically prepared membrane vesicles. Because (i) transport was electrogenic, (ii) a pNa drove uptake, and (iii) the number of sodium binding sites was approximately 1, it appeared that P. ruminicola possessed pentose/sodium symport mechanisms for the transport of arabinose and xylose at low substrate concentrations. Pentose uptake exhibited a low affinity for xylose or arabinose (>300M), and transport of xylose exhibited bi-phasic kinetics which suggested that a second sodium-dependent xylose transport system was present. Little study has been made on solute transport by Prevotella (Bacteroides) species and this work represents the first use of isolated membrane vesicles from these organisms.     

Physiological and morphological responses to elevated CO2 and a soil moisture deficit of temperate pasture species growing in an established plant community

Periods of limited soil water availability are a feature of many temperate pasture systems and these have the potential to modify pasture plant and community responses to elevated atmospheric CO2. Using large pasture turves, previously exposed to elevated CO2 concentrations of 350 or 700 mol mol^-1 for 324 d under well-watered conditions the morphological and physiological responses of pasture species growing at these CO2 concentrations were compared when subjected to a soil moisture deficit-and to recovery from the deficit-with those that continued to be well watered.Net leaf photosynthesis of Trifolium repens (C3 legume), Plantago lanceolata (C3) and Paspalum dilatatum (C4) was increased by exposure to elevated CO2, but there was no consistent effect of CO2 on stomatal conductance. At low soil moistures, net photosynthesis declined and stomatal conductance increased in these three species. There was a strong CO2 x water interaction in respect of net photosynthesis; in Trifolium repens, for example, elevated CO2 increased net photosynthesis by approximately 50% under well-watered conditions and this increased to over 300% when soil moisture levels reached their minimum values. Similar values were recorded for both Paspalum dilatatum and Plantago lanceolata. Potential water use efficiency (net photosynthesis/stomatal conductance) was increased by both exposure to elevated CO2 and drought.Leaf water status was measured in three species: Trifolium repens, Paspalum dilatatum and Holcus lanatus (C3). Total leaf water potential (t) and osmotic potential () were decreased by drought, but CO2 concentration had no consistent effect. t and were highest in the C4 species Paspalum dilatatum and lowest in the legume Trifolium repens.In the wet turves, rates of leaf extension of the C3 grasses Holcus lanatus and Lolium perenne at elevated CO2 were frequently higher than those at ambient CO2, but there was no effect of CO2 concentration on the rate recorded in the C4 grass Paspalum dilatatum or the rate of leaf appearance in the legume Trifolium repens. Drought reduced leaf extension rate irrespective of CO2 in all species, but in Holcus lanatus the reduction was less severe at elevated CO2. Immediately after the dry turves were rewatered the leaf extension rate on tillers of Holcus lanatus and Lolium perenne were higher than on tillers in the wet turves, but only at ambient CO2. Consequently, despite the greater leaf extension rate during the soil moisture deficit at elevated CO2, because of the overcompensation after rewatering at ambient CO2, total leaf extension over both the drying and rewetting period did not differ between CO2 concentrations for these C3 grass species. Further investigation of this difference in response between CO2 treatments is warranted given the frequent drying and wetting cycles experienced by many temperate grasslands.     

A complete citric acid cycle in assimilatory metabolism of Pelobacter acidigallici,a strictly anaerobic,fermenting bacterium

Pelobacter acidigallici is a strictly anaerobic bacterium that ferments trihydroxybenzenes to 3 mol acetate/mol substrate. The key intermediate linking the catabolic sequences to the formation of cell matter is acetyl-CoA. Since P. acidigallici is independent of further external electron donors, it must oxidize part of the acetyl-CoA to provide reducing equivalents for anabolism. In this study we demonstrate the presence of all enzymes necessary to operate a modified citric acid cycle, with activities sufficient to support growth. Unusual enzymes in the cycle are 2-oxoglutarate synthase and succinyl-CoA: acetoacetate CoA transferase. Anaplerotic reactions are catalyzed by pyruvate synthase, PEP synthetase and PEP carboxylase. No CO dehydrogenase, hydrogenase, or formate dehydrogenase activity could be detected. The phylogenetic implications of these findings with respect to the relatedness of P. acidigallici to gramnegative, sulfur-reducing bacteria by 16 S rRNA cataloguing are discussed.Abbreviations CoA coenzyme A - DCPIP 2,4-dichlorophenolindophenol - DTNB 5,5-dithiobis(2-nitrobenzoic acid) Ellman's reagent - DTT 1,4-dithiothreitol - methyl viologen 1,1-dimethyl-4,4-bipyridinium dichloride - PEP phosphoenolpyruvate - PMS phenazin methosulfate - Tricine N-[tris(hydroxymethyl)-methyl]-glycine - Tris tris(hydroxymethyl)aminomethane     

Scanning electron microscopic observations of chick embryo fibroblasts in vitro,with particular reference to the movement of cells under others

Summary Chick embryo fibroblasts in vitro have been studied with the scanning electron microscope. It has been found that when an advancing ruffled membrane reaches and crosses another cell, it retains contact with the substrate upon which it is moving. It is concluded that failure of contact inhibition is not explicable in terms of any hypothesis suggesting that advancing ruffled membranes adhere preferentially to the free (i. e. facing the nutrient medium) aspects of cells they encounter, rather than to their substrate.The Cambridge Scientific Instruments Stereoscan scanning electron microscope was provided by the Science Research Council (U. K.).     

Partial purification of endo- and exo-β-D-glucanase enzymes from Zea mays L. seedlings and their involvement in cell-wall autohydrolysis

The proteins dissociated from isolated Zea seedling cell wall using high-ionic-strength salt solutions have been found to include a number of enzymes which appear to participate in autolytic reactions of the cell wall. These enzymes caused extensive degradation of enzymatically inactive cell wall, liberating as much as 100 g/mg dry weight over a 48-h period. Lithium chloride (3M) was shown to be most effective in yielding protein and wall-degrading activities.Molecular-sieve chromatography of the cell-wall protein resolved endo--D-glucanase and exo--1,3-glucanase (EC 3.2.1.58) activities when Avena glucan and laminarin, respectively, were employed as substrates. The exoenzyme (molecular weight around 60,000) was strongly inhibited by inorganic mercury at a concentration which suppressed the release of monosaccharide from autolytically active cell wall. The endo--D-glucanase (MW around 26,000), which showed a marked preference for substrates of mixed-linkage, exhibited features indicating that it initiates the autolytic solubilization of wall glucan.Cell-wall -D-glucan, recovered as a component of an alkali-soluble cell-wall fraction, served as a substrate for the purified glucanases. Their hydrolysis pattern, assessed using gel exclusion chromatography and product analysis, confirmed that they hydrolyze -D-glucan. The products generated by the endoglucanase were similar in molecular-size distribution to those liberated from autolytically active-wall. Exoglucanase activity was required for extensive hydrolysis of -D-glucan in vitro.During coleoptile development the autolytic activity of the cell wall increased dramatically. This increased activity, however, did not parallel the growth potential of the tissue, but more closely reflected an increase in cell-wall -D-glucan, the primary substrate for autolytic reactions.These results were presented, in part, as papers at the annual meeting of the American Society of Plant Physiologists. Ohio State University, Columbus, in August 1979     

Karyosystematics of thePhleum alpinum polyploid complex (Poaceae)

The karyotypes of three taxa from thePhleum alpinum group of sect.Phleum (P. alpinum subsp.rhaeticum, 2n = 14,P. commutatum, 2n = 28, and informally namedP. commutatum, 2n = 14) were investigated by Giemsa C-banding. The overall similarity of diploid genomes suggests thatP. alpinum subsp.rhaeticum andP. commutatum are closely related — their karyotypes vary only with respect to their average amounts of telomeric heterochromatin. TheP. commutatum genome contains less telomeric heterochromatin than the genome ofP. alpinum subsp.rhaeticum, but in theP. alpinum group as a whole almost fluent transition between low (1.5%) and high (25.5%) amounts of telomeric heterochromatin was observed among populations. In the karyotype of tetraploidP. commutatum, seven distinguishable chromosome types were observed. Each of them is represented at somatic metaphase by four chromosomes. C-band structure of karyotype and average amount of telomeric heterochromatin suggest that this taxon has originated from hybridization between two related diploid forms of theP. commutatum — P. alpinum complex.     

Attraction of the bark beetle Tomicus piniperda and some other bark- and wood-living beetles to the host volatiles α-pinene and ethanol

The attraction of some bark- and ambrosia beetles as well as associated beetles to the host volatiles -pinene and ethanol was studied in field tests with flight barrier traps. Tomicus piniperda (L.) (Scolytidae), Thanasimus formicarius (L.) (Cleridae), and Rhizophagus ferrugineus (Payk.) (Rhizophagidae) were attracted by -pinene, while Hylurgops palliatus (Gyll.) and Trypodendron lineatum (Oliv.) (Scolytidae) were attracted by ethanol and Epuraea spp. (Nitidulidae) by both -pinene and ethanol. Combinations of -pinene and ethanol attracted high numbers of H. palliatus, T. lineatum, R. ferrugineus, Epuraea spp., and Glischrochilus spp. (Nitidulidae) and the catches increased with increasing release rates of ethanol. By contrast, lower numbers of T. piniperda were caught in traps baited with combinations of -pinene and ethanol than in traps baited with -pinene alone, and the catches of this species decreased with increasing release rates of ethanol. Traps baited with a combination of -pinene and ethanol or with -pinene alone caught similar numbers of T. formicarius. The results are discussed on the basis of species differences in preference for breeding substrate.

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Zusammenfassung Die Anlockung mehrerer Borkenkäfer und assoziierter Käferarten zu den flüchtigen Wirtsstoffen -Pinen und Äthanol wurde in Feldversuchen mit Flugbarrierenfallen studiert. Tomicus piniperda (L.) (Scolytidae), Thanasimus formicarius (L.) (Cleridae) und Rhizophagus ferrugineus (Payk.) (Rhizophagidae) wurden durch -Pinen angelockt, die Borkenkäfer Hylurgops palliatus (Gyll.) und Trypodendron lineatum (Oliv.) durch Äthanol und die Epuraea-Arten (Nitidulidae) durch sowohl -Pinen als auch Äthanol.Kombinationen von -Pinen und Äthanol lockten viele Individen von H. palliatus, T. lineatum, R. ferrugineus, Epuraea spp. und Glischrochilus spp. (Nitidulidae) an, und die Fänge nahmen mit zunehmender Äthanol-Abgabe zu. Umgekehrt wurden weniger T. piniperda in Fallen mit Kombinationen von -Pinen und Äthanol gefangen als in Fallen mit -Pinen allein, und die Waldgärtner-Fänge nahmen mit zunehmender Äthanol-Abgabe ab. Die Fänge von T. formicarius in Fallen mit einer Kombination von -Pinen und Äthanol unterschieden sich nicht von denen in Fallen mit nur -Pinen.Die Ergebnisse werden auf der Grundlage der Unterschiede zwischen den Arten in der Wahl des Brut-substrats besprochen.

     

The systematics of Porphyra: character evolution in closely related species

Isozymes, vegetative and reproductive morphology, seasonality, vertical and geographic distributions and chromosomes were compared for six pairs of putative sibling species of Porphyra (P. abbottae/P. torta, P. fallax subsp. fallax/P. fallax subsp. conwayae, P. amplissima/P. cuneiformis, P. fucicola/P. leucostica, P. miniata/P. variegata, P. umbilicalis/P. umbilicalis) and among five species in a complex (P. brumalis, P. kurogii, P. linearis, P. pseudolinearis, and P. purpurea.) Geographic distribution and zymograms for certain proteins showed the greatest change between species pairs: only one pair of species had identical distributions, and most species pairs were disjunct; every species had a different allozyme for GOT-1, whereas all species had apparently identical proteins for phycoerythrin. Seasonality and habitat exhibited moderate differentiation: Northeast Pacific sibling species were characterized by a high intertidal winter species pairing with a mid intertidal spring species, whereas all but one of the other species pairs exhibited nearly identical vertical distributions and seasonalities. There were few changes in morphology: most species pairs had essentially identical morphologies and coloration and the same arrangement of reproductive cells. Chromosome numbers and karyotypes were identical for species pairs and in the species complex. These results provide evidence for different rates of evolution of different characters in the genus Porphyra.     

Data consistency,yield and maintenance coefficient for the growth of Candida lypoytica and Pseudomonas aeruginosa on n-hexadecane

Summary When more than the minimum number of variables are measured, and measurement error is taken into account, the results of parameter estimation depend on which of the measured variables are selected for this purpose. The reparameterization of Pirt's models for growth produces multiresponse models with common parameters. By using the covariate adjustment technique, a unit variate linear model with covariates is obtained. This allows a combined point and interval estimates of biomass energetic yield and maintenance coefficient to be obtained using standard multiple regression programmes. When this method was applied using form I and form II of the Pirt's models, good combined estimates were obtained and compared. Using data from the literature for Candida lipolytica produced reliable results. However, for Pseudomonas aeruginosa, which has been known to produce intermediate products, a modified Pirt's model is required for a good estimate of the biomass energetic yield.Nomenclature a Mole of ammonia per quantity of organic substrate containing 1 g atom carbon, g mole/g atom carbon - b Moles of oxygen per quantity of organic substrate containing 1 g atom carbon, g mole/g atom carbon - c Moles of water per quantity of organic substrate containing 1 g atom carbon, g mole/g atom carbon; no of covariates included in model - d Moles of carbon dioxide per quantity of organic substrate containing 1 g atom carbon, g mole/g atom carbon - e _i Error terms in Eqs. (6–8) - l Atomic ratio of oxygen to carbon in organic substrate, dimensionless - m Atomic ratio of hydrogen to carbon in organic substrate, dimensionless - m _e Rate of organic substrate consumption for maintenance, g equiv. of available electrons in biomass (h) or kcal/Kcal of biomass(h) - n Atomic ratio of oxygen to carbon in biomass, dimensionless - p Atomic ratio of hydrogen to carbon in biomass, dimensionless - Q _{CO 2} Rate of evolution of carbon dioxide, g moles/g dry wt (h) - Q _{O 2} Rate of oxygen consumption, g moles/g dry wt (h) - Q _s Rate of organic substrate consumption g/g dry wt (h) - q Atomic ratio of nitrogen to carbon in biomass, dimensionless - r Atom ratio of hydrogen to carbon in products, dimensionless; the number of parameters of interest - s Atomic ratio of oxygen to carbon in products, dimensionless - t Atomic ratio of nitrogen to carbon in products, dimensionless - r Mean of k responses in Eq. (10) - x _ki Kth response in the ith observation - y _c Biomass carbon yield (fraction of organic substrate carbon in biomass), dimensionless - z _i Covariate matrix - z Fraction of organic substrate carbon in products, dimensionless - a _i Parameters associated with covariates - _s Reductance degree of biomass, equivalents of available electrons per gram atom carbon - Reductance degree of organic substrate, equivalents of available electrons per gram atom carbon - Fraction of energy in organic substrate which is evolved as heat, dimensionless - Fraction of available electrons transferred to biomass; biomass energetic yield - True growth yield - Specific growth rate, h^-1 - _p Fraction of available electrons incorporated into products; product energetic yield - Correlation coefficient - Mass fraction carbon - ² Mean square error of model (10)     

The promoter of the beta-glucosidase gene from Kluyveromyces fragilis contains sequences that act as upstream repressing sequences in Saccharomyces cerevisiae

Summary The relationship between the promoter length of the Kluyveromyces fragilis -glucosidase gene and the level of its expression in Saccharomyces cerevisiae was studied by gene fusion between deleted promoter fragments of various lengths and the promoterless -galactosidase gene of Escherichia coli. The removal of a region from position-425 to-232 led to a tenfold increase in the expression of the gene. The same results were obtained for the reconstructed -glucosidase gene with the same promoter length. It is likely that the deletion of this part of the promoter removes negative regulatory elements which are functional in Saccharomyces cerevisiae. This increase in activity is the main event which may explain the high increase in gene expression (60-fold) previously observed for an upstream deletion obtained during subcloning experiments of the -glucosidase gene. It is also shown that the expression of the gene greatly depends upon the nature of the recipient strain, the growth phase of the cell and that of the vector carrying it.     

A novel eye morphology induced by a P element in somatic tissue of Drosophila melanogaster.

Summary We found a specific eye morphology designated as Square, which is induced when some Drosophila melanogaster strains harboring P elements are crossed with the 2–3 strain carrying a modified P element, P[ry ⁺, 2–3], which produces transposase in somatic tissue. This phenotype was dominant and also induced in the reciprocal crosses. Square was induced when the 2–3 strain was crossed with Q and M strains such as the sn^w (M) strain carrying three small P elements but not with P strains. Inheritance of Square was also tested and its phenotype was not transmitted to the next generation. These results suggest that Square is caused by the transposition of P elements in somatic cells.     

Purification and characterization of a thermostable and acid-stable phytase from Pichia anomala

Phytase of Pichia anomala was purified to near homogeneity by a two-step process of acetone precipitation followed by anion exchange chromatography using DEAE-Sephadex. The enzyme had a molecular weight of 64 kDa. It was optimally active at 60 °C and pH 4.0. This enzyme was found to be highly thermostable and acid-stable, with a half life of 7 and 8 days at 60 °C and pH 4.0 respectively. At 80 °C, the half life of phytase could be increased from 5 to 30 min by the addition of materials such as sucrose, lactose and arabinose (10% w/v). The enzyme exhibited a broad substrate specificity, since it acted on p-nitrophenyl phosphate, ATP, ADP, glucose-6-phosphate besides phytic acid. The K _m value for phytic acid was 0.20 mM and V _max was 6.34 mol/mg protein/min. There was no requirement of metal ions for activity. SDS was observed to be highly inhibitory to phytase activity. Sodium azide, DTT, -mercaptoethanol, EDTA, toluene, glycerol, PMSF, iodo-acetate and N-bromosuccinimide did not show inhibitory activity. The enzyme was inhibited by 2,3-butanedione, indicating the involvement of arginine residues in catalysis. Phytase activity was not inhibited in the presence of inorganic phosphate upto 10 mM. The shelf life of the enzyme was 6 months at 4 °C and there was no loss in the activity on lyophilization. Very few studies have been done on purification of yeast phytases. This is the first report on purification and characterization of phytase from P. anomala. The enzyme is unique in being thermostable, acid-stable, exhibiting broad substrate specificity and in not requiring metal ions for its activity. The yeast biomass containing phytase appears to be suitable for supplementing animal feeds to improve the availability of phosphorus from phytates.     

American Cockroach (Periplaneta americana) Synthesizes Carotenoids from the Precursor [14C]Mevalonic Acid Pyrophosphate

The level of an important carotenoid (-carotene) in the gut of Periplaneta americana depends on the content of the carotenoid in food: a carotenoid-fortified diet causes accumulation of -carotene up to 10 g/g wet weight, while on a carotenoid-deficient diet the level of this substance is low (0.7 g/g wet weight). In the eye, in contrast to the gut, a constant level of -carotene (1.3-1.4 g/g wet weight) is found regardless of the diet. This phenomenon remained unchanged over three years of feeding of the cockroaches with the carotenoid-deficient diet, suggesting that P. americana produces carotenoids by de novo biosynthesis. This suggestion was confirmed in experiments using intraperitoneal injection of the exogenous carotenoid biosynthesis precursor [¹⁴C]mevalonic acid pyrophosphate followed by extraction of carotenoid and chromatographic purification of the labeled product. Injection of 3.4 nmoles [¹⁴C]mevalonic acid pyrophosphate transiently increased the -carotene content in eyes on days 2 and 4 after injection of the label. Purification of radiolabeled carotenoids from eye and gut by the transfer of carotenoids into a less polar solvent, alkaline hydrolysis (saponification), and chromatography on alumina and cellulose columns decreased the specific radioactivity to a constant level that cannot be further decreased by repeated chromatography. The elution profile of these purified preparations of -carotene after chromatography is characterized by coincidence of symmetric peaks of count and absorption. We suggest that to create the optimal carotenoid concentration in the eye, P. americana uses two biochemical mechanism: 1) it accumulates carotenoids in reserve in the gut when abundant supplies of carotenoids are available in the diet; 2) it synthesizes carotenoids de novo when its food is deficient in these compounds.     

Subtle topographical differences along a floodplain promote different plant strategies among Paspalum dilatatum subspecies and populations

It was hypothesised that subtle topographical differences might cause the existence of ecotypes along a floodplain. The apomict grass Paspalum dilatatum subspecies dilatatum inhabits flood‐prone lowlands as well as nearby uplands in the floodplains of Argentina, while the sexual P. dilatatum subspecies flavescens almost exclusively inhabits the uplands. The aim of the present study was to identify the different traits that allow these P. dilatatum populations to inhabit different habitats. Plants of P. dilatatum were reciprocally transplanted between uplands and lowlands. Morphophysiological traits related to flooding tolerance were measured during a flood. Subspecies dilatatum from the uplands and subspecies flavescens showed a high physiological performance in the uplands but a considerable decrease in stomatal conductance, net photosynthesis rates and tiller number in the flooded lowlands. In contrast, the subspecies dilatatum from the lowlands showed relatively lower and stable stomatal conductance, photosynthesis rates and leaf water potential at both sites. Subspecies dilatatum from the lowlands outperformed upland populations at the lowland site with respect to tillering. Leaves of subspecies dilatatum from the lowlands that had grown at the lowland habitat had a lower blade/sheath proportion than leaves of plants transplanted to the uplands. This behavior did not occur in both upland populations. Results suggest that dilatatum Lowland plants have the typical strategy of stress‐tolerant genotypes and that the upland populations are adapted to habitats where competitive species are selected. In conclusion, habitats with subtle differences in topographic level can favour both ecotypic differentiations within an apomict subspecies but also the maintenance of morphophysiological similitudes between coexisting upland populations belonging to different subspecies.     

Compartmentation of the early steps of cholesterol biosynthesis in mammalian liver

Summary Cholesterol synthesis was studied in the isolated perfused rat liver and with cell-free preparations by incorporation measurements of³H from³HOH and of carbon label from [1-¹⁴C]-acetate. Using specific inhibitors such as (-)-hydroxycitrate, kynurenate, and avidin the following conclusions were reached:Fatty acid and cholesterol biosynthesis share a common substrate pool of cytoplasmic acetyl-CoA. The substrate of mevalonate synthesis is furnished by an extramitochondrial pathway of-hydroxy--methylgluraryl-CoA synthesis, which does not include malonyl-CoA. This favors the assumption of a sequence including cytoplasmic thiolase and-hydroxy--methylglutaryl-CoA synthase.Besides its inhibitory action on ATP citrate lyase (-)-hydroxycitrate was found to stimulate acetyl-CoA carboxylase.Acetyl-CoA synthetase activity of liver is localized predominantly in the cytoplasm. The regulatory behavior of the cytoplasmic enzyme points to a lipogenetic function.The control of cholesterol biosynthesis and the role of cytoplasmic acetyl-CoA synthetase in the maintenance of the extramitochondrial acetyl-CoA pool are considered in light of the reported findings.     

Microbial transformations in a cyclodextrin medium. Part 2. Reduction of androstenedione to testosterone by Saccharomyces cerevisiae

Summary An intensive and systematic investigation of the reductive transformation of androstenedione (AD) to testosterone by Saccharomyces cerevisiae was undertaken in the presence of natural and chemically modified cyclodextrins (CD). The bioconversion was significantly larger in the presence of - and -CD and hydroxypropyl--CD b but only slight in the presence of -CD and dimethyl- and trimethyl--CD. The performance of the various cyclodextrin media was interpreted in the light of the measured phase solubility diagrams of AD. Further investigation focused on biotransformation of the -CD-androstenedione complex, the formation of which was studied by differential scanning calorimetry and X-ray powder diffractometry and stoichiometry determined by ¹H-nuclear magnetic resonance. A mechanism whereby CDs reduce the effective inhibitory concentrations of substrate and product as well as facilitate transport of the complexed substrate through the yeast cell wall has been suggested for the CD-promoted biotransformation. Offprint requests to: R. Bar     

Growth,acetylene reduction activity and localization of nitrogenase in relation to vesicle formation in Frankia strains Cc1.17 and Cp1.2

A comparative study was conducted on the effect of NH₄Cl on growth, vesicle formation and formation of nitrogenase of Frankia strains Cc1.17 and Cp1.2, derived from root nodules of Colletia cruciata and Comptonia peregrina, respectively. On a medium without combined nitrogen (P-N), both strains formed spherical cells, called vesicles, like many other Frankia strains. Data are presented on the number of vesicles per mg protein, after cultivation in media with sodium propionate as C-source without combined nitrogen (P-N) or with 0.2 g NH₄Cl/l (P+N). Strain Cp1.2 as may other Frankia strains, showed on P+N medium a very strong reduction of vesicle formation of 99% relative to the number of vesicles formed on P-N medium, after 11 days growth. However, in strain Cc11.17 this reduction was only 70%. The occurence of relatively large numbers of vesicles in P+N media has not yet been reported for other Frankia strains. No acetylene reduction activity was found in NH ₄ ⁺ -grown cells. The regulation of induction of nitrogenase in Frankia by NH₄Cl was tested by immuno-gelectrophoresis using antisera against nitrogenase of Rhizobium leguminosarum PRE. The component I of the enzyme showed crossreactivity while the component II had only a weak crossreaction. The experiments indicated that no nitrogenase was detectable in the NH ₄ ⁺ -grown cells. For the localization of nitrogenase, relative amounts of the enzyme were compared in whole cells and vesicle-enriched fractions. Western blots showed a significant enrichment of nitrogenase in the vesicle fractions, which indicated that most of the nitrogenase was localized in the vesicle.