Mechanical transmission of beet yellows virus toChenopodium quinoa Willd. andChenopodium foliosum (Moench) Asch.

Beet yellows virus (BYV) was mechanically transmitted by sap from sugar-beet plants, infected with BYV, to the plants ofChenopodium quinoa Willd. and ofChenopodium foliosum (Moench) Asch. Mechanical transmission of BYV to the plants ofTetragonia expansa Murr. failed. Infectious material was homogenized in phosphate buffer with veronal and EDTA, pH 7–8. Experimental plants were darkened three days before infection and kept at a temperature of 5°C. Plants ofC. quinoa Willd. were decapitated. Back transmissions fromC. quinoa Willd. andC. foliosum (Moench) Asch. infected with BYV, to sugar-beet plants were carried out by the aveidMyzus persicae Sulz. These transmissions were positive. Filamentous particles of BYV, of an average length 1275 nm, were found in plants ofC. quinoa Willd. andC. Foliosum (Moench) Asch., infected with BYV.     

D-amino acids in the cell pool of bacteria

About 30 different bacterial species were tested for the possible presence of freed-amino acids in their cell pool. Gram-positive bacteria particularly the species of the genusBacillus have a fairly large pool of freely extractabled-amino acids. Varied quantities of freed-amino acids were detected inBacillus subtilis B₃,Bacillus subtilis Marburg,Bacillus licheniformis, Bacillus brevis, Bacillus stearothermophilus, Lactobacillus fermenti, Lactobacillus delbrueckii, Staphylococcus aureus andClostridium acetobutylicum. The individual components ofd-amino acids were identified in 5Bacillus species referred to above,d-alanine is the major component; the otherd-amino acids identified are aspartic acid, glutamic acid, histidine, leucines, proline, serine and tyrosine. Thed-amino acid pool size inBacillus subtilis B₃ varies with different culture conditions. The pool size is maximum when growth temperature is 30°C and it fluctuates with change in pH of the medium. The maximum quantity ofd-amino acids could be recovered when the culture was at mid log phase. O₂ supply to the medium has little effect ond-amino acid pool size. The starvation of cells leads to depletion of thed-amino acid pool which is exhausted almost completely within 4 hours by incubation in nutrient-free medium.     

Chromosome counts and chromosome morphology of some selected species

In the years 1976–1981 we studied chromosome counts and karyotypic formulae of the following 29 species of plants from 41 localities (of these 6 from Bohemia, 32 from Moravia, 3 from Slovakia):Batrachium baudotii (Godron) F. W. Schultz,Chenopodium rubrum L.,C. polyspermum L.,C. murale L.,C. ficifolium Sm.,C. opulifolium Schrader ex DC. inLam. et DC.,C. strictum Roth [subsp.strictum, subsp.glaucophyllum (Aellen)Aellen inJust etAellen, subsp.striatiforme Uotila],Arenaria grandiflora L.,Illecebrum verticillatum L.,Spergula morisonii Boreau inDuchartre,Spergularia marginata (DC. inLam. et DC.)Kittel S. marina (L.)Griseb.,S. rubra (L.) J. etC. Presl,Silene conica L.,Sisymbrium loeselii L.,S. volgense Bieb. exE. Fourn.,S. orientale L. [subsp. orientale, subsp.macroloma (A. Pomel)Dvo?ák],S. officinale (L.)Scop.,Descurainia sophia (L.)Webb exPrantl inEngler etPrantl,Nasturtium officinale R. Br. inAiton,Barbarea arcuata (Opiz inPresl J. et C.)Reichenb.,Lunaria annua L.,Soldanella montana Willd.,S. carpatica Vierh. inUrban etGraebner,Lotus tenuis Waldst. etKit. exWilld.,L. uliginosus Schkuhr,Trigonella monspeliaca L.,Geranium sibiricum L.,Lactuca tatarica (L.)C. A. Meyer.     

Characterization of a recombinant l-fucose isomerase from Caldicellulosiruptor saccharolyticus that isomerizes l-fucose, d-arabinose, d-altrose, and l-galactose

A recombinant l-fucose isomerase from Caldicellulosiruptor saccharolyticus was purified as a single 68 kDa band with an activity of 76 U mg^?1. The molecular mass of the native enzyme was 204 kDa as a trimer. The maximum activity for l-fucose isomerization was at pH 7 and 75°C in the presence of 1 mM Mn²⁺. Its half-life at 70°C was 6.1 h. For aldose substrates, the enzyme displayed activity in decreasing order for l-fucose, with a k _cat of 11,910 min^?1 and a K _m of 140 mM, d-arabinose, d-altrose, and l-galactose. These aldoses were converted to the ketoses l-fuculose, d-ribulose, d-psicose, and l-tagatose, respectively, with 24, 24, 85, 55% conversion yields after 3 h.     

Mortality factors of satin moth,Leucoma salicis [Lep.: Lymantriidae], in aspen forests in Maine

Natural control agents of the satin moth,Leucoma salicis (L.) were examined in 2Populus grandidentata Michaux stands. Highest mortality occurred in overwintering larvae, with the causal agents 2 fungi,Paecilomyces sp. andHirsutella gigantea Petch, a factor causing death symptomatic of a pathogen, the parasiteEupteromalis hemipterus (Walker) and death from unknown causes. Mortality fromPaecilomyces sp. andE. hemipterus was reduced where overwintering sites were covered with burlap cloth. Parasites recovered from larvae and pupae included the braconidsApanteles melanoscelus (Ratzeburg) andMeteorus versicolor (Wesmeal), the ichneumonidCoccygomimus pedalis (Cresson), the tachinidsCompsilura concinnata (Meigen),Carcelia laxifrons Villeneuve,Tachinomyia variata Curran, and the sarcophagidsSarcophaga aldrichi Parker andAgria housei Shewell. Larval and pupal predators included the carabidCalosoma frigidum Kirby, pentatomids, and birds, particularly black-billed cuckoos,Coccyzus erythrophthaimus (Wilson). Eggs were parasitized by the scelionidTelenomus prob.californicus Ashmead and the trichogrammidTrichogramma minutum (Riley). Predators of adult satin moths included the hermit thrush,Hylocichla guttata (Pallas), and pentatomid bugs.     

Survey and distribution ofCybocephalidae [Coleoptera] in Israel

Nine species ofCybocephalus were found in a survey conducted throughout Israel:C. micans (Reitter),C. nigriceps nigriceps (J. Sahiberg),C. nigriceps sinister Endrödy-Younga,C. aegyptiacus Endrödy-Younga,C. mediterraneus Endrödy-Younga,C. pullus Endrödy-Younga,C. fodori minor Endrödy-Younga,C. membranaceus (Reitter) andCybocephalus sp. n.C. micans andC.n. nigriceps are the most prevalent: the former in the Coastal Plain on citrus and the latter in the Arava region on date palms. In most cases the population density of the predator appeared to be related to that of the prey. Armoured scale insects(Homoptera: Diaspididae) were the main prey ofCybocephalus.     

Bacidina genus novum familiaeLecideaceae s. lat. (Ascomycetes lichenisati)

The following eleven species currently classified in the generaBacidia s. lat. andCatillaria s. lat. are transferred to the new genusBacidina Vězda gen. n. (Lecideaceae s. lat.):Bacidina apiahica (Müll. Arg.) comb. n.,B. chloroticula (Nyl.)Vězda etPoelt comb. n.,B. egenula (Nyl.) comb. n.,B. inundata (Fr.) comb. n.,B. mirabilis (Vězda) comb. n.,B. neglecta (Vězda) comb.n.,B. pallidocarnea (Müll. Arg.) comb. n.,B. phacodes (Koerb.) comb.n.,B. scutellifera (Vězda) comb.n.,B. vasakii (Vězda) comb.n., andB. ziamensis (Vězda) comb.n.     

LignicolousHyphomycetes from Czechoslovakia 5.Septonema,Hormiactella andLylea

Three genera of lignicolousHyphomycetes Septonema Corda,Hormiactella Saac. andLylea Morgan-Jones are discussed. Illustrations and determination keys are provided. Five species ofSeptonema—S. fasciculare (Corda) Hughes,S. leptaleum (Ellis & Harkn.) Hughes,S. pinicola Hol.-Jech.,S. secedens Corda andS. laricium Hol.-Jech.—and two species ofHormiactella—H. fusca (Preuss) Sacc. andH. asetosa Hol.-Jech.—have been found in Czechoslovakia. A new speciesS. pseudobinum Hol.-Jech. is described from Romania.Septonema tetracoilum (Corda Hughes is accommodated in the genusLylea Morgan-Jones.     

A d-psicose 3-epimerase with neutral pH optimum from Clostridium bolteae for d-psicose production: cloning, expression, purification, and characterization

d-Tagatose 3-epimerase family enzymes can efficiently catalyze the epimerization of free keto-sugars, which could be used for d-psicose production from d-fructose. In previous studies, all optimum pH values of these enzymes were found to be alkaline. In this study, a d-psicose 3-epimerase (DPEase) with neutral pH optimum from Clostridium bolteae (ATCC BAA-613) was identified and characterized. The gene encoding the recombinant DPEase was cloned and expressed in Escherichia coli. In order to characterize the catalytic properties, the recombinant DPEase was purified to electrophoretic homogeneity using nickel-affinity chromatography. Ethylenediaminetetraacetic acid was shown to inhibit the enzyme activity completely; therefore, the enzyme was identified as a metalloprotein that exhibited the highest activity in the presence of Co²⁺. Although the DPEase demonstrated the most activity at a pH ranging from 6.5 to 7.5, it exhibited optimal activity at pH 7.0. The optimal temperature for the recombinant DPEase was 55 °C, and the half-life was 156 min at 55 °C. Using d-psicose as the substrate, the apparent K _m, k _cat, and catalytic efficiency (k _cat/K _m) were 27.4 mM, 49 s^?1, and 1.78 s^?1 mM^?1, respectively. Under the optimal conditions, the equilibrium ratio of d-fructose to d-psicose was 69:31. For high production of d-psicose, 216 g/L d-psicose could be produced with 28.8 % turnover yield at pH 6.5 and 55 °C. The recombinant DPEase exhibited weak-acid stability and thermostability and had a high affinity and turnover for the substrate d-fructose, indicating that the enzyme was a potential d-psicose producer for industrial production.     

Metabolic engineering Corynebacterium glutamicum for the l-lysine production by increasing the flux into l-lysine biosynthetic pathway

The experiments presented here were based on the conclusions of our previous results. In order to avoid introduction of expression plasmid and to balance the NADH/NAD ratio, the NADH biosynthetic enzyme, i.e., NAD-dependent glyceraldehyde-3-phosphate dehydrogenase (GADPH), was replaced by NADP-dependent GADPH, which was used to biosynthesize NADPH rather than NADH. The results indicated that the NADH/NAD ratio significantly decreased, and glucose consumption and l-lysine production drastically improved. Moreover, increasing the flux through l-lysine biosynthetic pathway and disruption of ilvN and hom, which involve in the branched amino acid and l-methionine biosynthesis, further improved l-lysine production by Corynebacterium glutamicum. Compared to the original strain C. glutamicum Lys5, the l-lysine production and glucose conversion efficiency (α) were enhanced to 81.0 ± 6.59 mM and 36.45 % by the resulting strain C. glutamicum Lys5-8 in shake flask. In addition, the by-products (i.e., l-threonine, l-methionine and l-valine) were significantly decreased as results of genetic modification in homoserine dehydrogenase (HSD) and acetohydroxyacid synthase (AHAS). In fed-batch fermentation, C. glutamicum Lys5-8 began to produce l-lysine at post-exponential growth phase and continuously increased over 36 h to a final titer of 896 ± 33.41 mM. The l-lysine productivity was 2.73 g l^?1 h^?1 and the α was 47.06 % after 48 h. However, the attenuation of MurE was not beneficial to increase the l-lysine production because of decreasing the cell growth. Based on the above-mentioned results, we get the following conclusions: cofactor NADPH, precursor, the flux through l-lysine biosynthetic pathway and DCW are beneficial to improve l-lysine production in C. glutamicum.     

Observation of algal colonization on Acropora aspera killed by Acanthaster planci

Algae started colonizing branches of the coral Acropora aspera (Dana) killed by the sea star Acanthaster planci (Linnaeus) within less than 24 hours. Two blue-greens ((Microcoleus lyngbyaceus (Crouan) Ag. and Hormothamnion solutum B. & F.)) dominated the early community but became less abundant than a brown ((Giffordia indica (Sonder) Papenfuss & Chihara)) after 26 days.     

Cytotaxonomic study ofTragopogon L. in czechoslovakia

Karyotypes ofTragopogon orientalis L. subsp.orientalis, T orientalis L. subsp.leiocarpos (Sauter)Trnka,T. pratensis L.,T. minor Miller,T. dubius Scop. subsp.dubius andT. dubius Scop. subsp.major (Jacq.)Vollmann were studied. The occurrence in Slovakia ofT. pratensis was karyologically proved.     

Parasites of rice stemborers in Sarawak (Malaysian Borneo)

Observations on parasites were made during a study of the following rice stem-borers in Sarawak (Malaysian Borneo):Tryporyza incertulas (Walker),T. innotata (Walker),Chilo suppressalis (Walker)C. auricilia (Dudgeon), andSeamia inferens (Walker). Egg-parasitism was often high, but that of the larval and pupal stages generally very low. Between 40–80% of theTryporyza eggs were parasitised byTelenomus rowani (Gahan), while 30–50% were attacked byTetrastichus schoenobii Ferrière. About 40–90% of the eggs ofChilo were parasitised byTrichogramma? japonicum Ashmead and 5–26% byTelenomus dignus (Gahan). Only 0.4–3% of theTryporyza larvae were parasitised by a Braconid,Rhaconotus schoenobivorus (Rohwer), whileBracon chinensis Szepligeti attacked 0.2–0.7% of the larvae ofC. suppressalis. Parasitism ofSesamia larvae byApanteles flavipes Cameron was equally low, never exceeding 2%. Pupal parasitism was somewhat higher.Tetrastichus israeli (Mani & Kurian) attacked 8% and 18% of the pupae ofC. suppressalis andS. inferens, respectively, while the Ichneumonid,Xanthopimpla stemmator (Thunberg) attacked up to 3% of the pupae of the former species. The immature stages of some of these parasites are described.     

Characterization of a recombinant l-rhamnose isomerase from Bacillus subtilis and its application on production of l-lyxose and l-mannose

The gene of an l-rhamnose isomerase (RhaA) from Bacillus subtilis was cloned to the pET28a(+) and then expressed in the E. coli ER2566. The expressed enzyme was purified with a specific activity of 3.58 U/mg by His-Trap affinity chromatography. The recombinant enzyme existed as a 194 kDa tetramer and the maximal activity was observed at pH 8.0 and 60°C. The RhaA displayed activity for l-rhamnose, l-lyxose, l-mannose, d-allose, d-gulose, d-ribose, and l-talose, among all aldopentoses and aldohexoses and it showed enzyme activity for l-form monosaccharides such as l-rhamnose, l-lyxose, l-mannose, and l-talose. The catalytic efficiency (k _cat/K _m) of the recombinant enzyme for l-rhamnose, l-lyxose, and l-mannose were 7,460, 1,013, and 258 M/sec. When l-xylulose 100 g/L and l-fructose 100 g/L were used as substrates, the optimum concentrations of RpiB were determined with 6 and 15 U/mL, respectively. The l-lyxose 40 g/L was produced from l-xylulose 100 g/L by the enzyme during 60 min, while l-mannose 25 g/L was produced from l-fructose 100 g/L for 80 min. The results suggest that RhaA from B. subtilis is a potential producer of l-form monosaccharides.     

Parasitism ofPhthorimaea operculella [Lep.: Gelechiidae] larvae in Queensland

Parasitism ofPhthorimaea operculella (Zeller) larvae on potato foliage was examined intensively in the Lockyer Valley, south-eastern Queensland from 1975–78 and extensively from other hosts and areas of Queensland. The % parasitism in the Lockyer Valley exceeded 50% in 29 of the 36 collections. The parasite species were dominated by the introducedCopidosoma desantisi Annecke & Mynhardt (Encyrtidae) andOrgilus lepidus Muesebeck (Braconidae) which together accounted for 92.6% of parasite numbers recorded. In more northern areas of Queensland, the dominant parasite species found was the introducedApanteles subandinus Blanchard (Braconidae). Other hymenopterous parasites found wereMicrochelonus curvimaculatus Cameron (Braconidae), Elasmus funereus Riek (Elasmidae) andTemelucha minuta (Morley) (Ichneumonidae).     

The effect of prey density on the functional and numerical reponses of three species of predatory mites

Functional and numerical responses of the predators:Phytoseiulus persimilis Athias-Henriot,Metaseiulus occidentalis (Nesbitt), andAmblyseius chilenensis (Dosse) [Acarina, Phytoseiidae] were observed at prey (Tetranychus urticae Koch [Acarina, Tetranychidae]) densities up to 300 prey/6.45 cm². Neither functional nor numerical response curves revealed any prey-predator interference effects, i.e.: the dome-shaped response curves (Holling, 1961), did not occur.     

The parasitoid complex of three noctuids [Lep.] in a northern Florida cropping system: Seasonal occurrence,parasitization, alternate hosts,and influence of host-habitat

Parasitoids of the cabbage looper,Trichoplusia ni (Hübner), the soybean looper,Pseudoplusia includens (Walker), and the tobacco budworm,Heliothis virescens (F.) were characterized in a 3.2-ha model of a north Florida (U.S.A.) cropping system (including tobacco (Nicotiana tabacum L.), soybeans (Glycine max (L.)Merr. and 18 other crops) not treated with chemical pesticides. The study was for a 2 yr-period; a minimum of three 0.0004-ha sections of row, or 0.0001-ha sections in broadcast or drilled crops were sampled weekly. In addition, sweeps with a net and some other sampling techniques were used in some crops.Litomastix truncatella (Dalman),Meteorus autographae Muesebeck, andVoria ruralis Fallen were the most important larval parasitoids recovered from cabbage loopers;Trichogramma spp. were by far the major egg parasitoid. Parasitization of eggs and larvae in crucifers (Brassica oleracea L.) ranged from 0 to 55% and 0 to 100%, respectively, and was generally highest during the spring and fall. Parasitization of cabbage looper immatures was highest in tomatoes (Lycopersicon esculentum Mill.). Parasitism by the parasitoid complex for the soybean looper larvae was high but eggs in soybeans were seldomly attacked by parasitoids. Tobacco budworm eggs were rarely parasitized in tobacco but were frequently parasitized in tomatoes and okra (Abelmoschus esculentus (L.)Medik). Parasitization of tobacco budworm larvae in tobacco was usually over 50% and was mostly byCardiochiles nigriceps Viereck; fewC. nigriceps were found from the other plants.     

Low Energy Conformations for Gonadotropin-Releasing Hormone with d- and l-Amino Acid Substitutions for Gly 6: Possible Receptor-Bound Conformations

In the preceding paper, using ECEPP, including the effects of water, and the chain build-up procedure, we computed the low energy structures for GnRH and found that there were no distinct low energy structures or structures with high statistical weights. To attempt to deduce possible structures of GnRH that may bind to the GnRH receptor, we computed the low energy structures for GnRH peptides that have l- and d-amino acids substituting for Gly 6. The l-amino acid-substituted peptides (l-Ala and l-Val) have very low or no affinity for the receptor and on activity (release of FSH and LH) while the d-Ala-, d-Leu-, d-Trp- and d-Phe-substituted peptides have significantly higher relative affinities and activities than those for native GnRH; the d-Val-substituted peptide has about one-third of the affinity and activity as native GnRH. Unlike native GnRH, our computations suggest that both sets of peptides form well-defined structures in water: the l-amino acid-substituted peptides are predominantly α-helical while the d-amino acid-substituted peptides adopted E*A A A E D*(C*) A E C A(C*) and minor variants of these structures. By eliminating structures that lay in common to the d-Ala and l-Val peptides and further eliminating structures that differed between the d-Ala and d-Leu peptides, we reduced the number of possible distinct binding conformations to 254. Searching for structures among these 254 conformations that had relative statistical weights that paralleled their relative affinities, we found two candidate structures: D*E A A E C*A E C A and D*G A A E D*A E C G*, both of which have conformations for residues 3–9 that are similar to the computed most probable structures for the d-amino acid-substituted GnRH peptides in water.     

Further karyological studies of the Mongolian flora

The paper gives the chromosome number for 50 species of the Mongolian flora. Some of the counts appear to be the first findings for the species. They are:Draba eriopoda Turcz. exLedeb. 2n=16,Lychnis sibirica L. 2n=24,Papaver pseudocanescens M. Popov 2n=42,Thymus baicalensis Serg. 2n=28 andViola gmeliniana Schultes 2n=24.     

Overexpression of d-psicose 3-epimerase from Ruminococcus sp. in Escherichia coli and its potential application in d-psicose production

The d-psicose 3-epimerase (DPE) gene from Ruminococcus sp. was cloned and overexpressed in Escherichia coli. The recombinant protein was purified and characterized. It was optimally active at pH 7.5–8.0 and 60?°C. Activity was not dependent on the presence of metal ions; however, it became more thermostable with added Mn²⁺. The K _m of the enzyme for d-psicose (48?mM) was lower than that for d-tagatose (230?mM), suggesting that d-psicose is the optimum substrate. More importantly, the thermostability of the novel DPE from Ruminococcus is the strongest among all of the d-psicose and d-tagatose 3-epimerases and may be suitable for the industrial production of d-psicose from fructose.