Die Hemmung der Phytochrominduzierten Photomorphogenese („Positive” Photomorphosen) des Senfkeimlings (Sinapis alba L.) Durch Actinomycin D und Puromycin

Zusammenfassung Die positiven Photomorphosen Öffnung des Hypokotylhakens und Entfaltung der Kotyledonen können ganz ähnlich wie die phytochrominduzierte Anthocyansynthese und andere positive Photomorphosen durch Actinomycin D und Puromycin gehemmt werden. Man kann daraus schließen, daß diese beiden photomorphogenetischen Reaktionen des Senfkeimlings ebenfalls durch eine von P₇₃₀ über eine Signalkette ausgelöste Aktivierung von potentiell aktiven Genen veranlaßt werden.

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The inhibition of phytochrome-mediated photomorphogenesis (positive photoresponses) by actinomycin D and puromycin in the mustard seedling (Sinapis alba L.)

Summary The many photochrome-mediated photoresponses of a seedling (Sinapis alba L., white seeded mustard) can be divided into 3 categories: positive, negative, and complex photoresponses. Positive photoresponses are those which are characterized by an initiation or a promotion of biosynthetic or growth processes (Mohr, 1966b). Phytochrome-mediated anthocyanin synthesis is the prototype of a positive photoresponse. It has been shown in previous papers (e.g. Lange and Mohr, 1965; Mohr et al., 1965) that positive photoresponses can be specifically inhibited by actinomycin D and puromycin. It has been concluded that in the case of positive photoresponses P₇₃₀ (the active phytochrome) exerts its function through differential gene activation.—In the present paper it has been demonstrated that phytochrome-mediated positive photoresponses of the mustard seedling like opening of the hypocotylar hook and unfolding of the cotyledons can be inhibited by relatively low doses of actinomycin D and puromycin in very much the same way as anthocyanin synthesis or cotyledon enlargement is inhibited. It has been concluded that in these cases too the action of P₇₃₀ must be attributed to an activation of potentially active genes in the manner postulated on the basis of the data on anthocyanin synthesis.

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Die Arbeit wurde durch Sachbeihilfen der Deutschen Forschungsgemeinschaft und der Stiftung Volkswagenwerk (an Prof. Mohr) ermöglicht.     

Uptake of sewage derived nitrogen by<Emphasis Type="Italic"> Ulva rigida</Emphasis> (Chlorophyceae) in Bahía Nueva (Golfo Nuevo,Patagonia, Argentine)

Uptake kinetics of nitrogen derived from sewage–seawater mixtures (2.5–20% v/v effluent) were determined in the laboratory for Ulva rigida (Chlorophyceae) native from Bahía Nueva (Golfo Nuevo, Patagonia, Argentine). In terms of nitrogen concentration, experimental enrichment levels varied between 53.7 and 362.3M of ammonium and between 0.77 and 6.21M of nitrate+nitrite. Uptake rates were fitted to the Michaelis–Menten equation, with the following kinetic parameters: ammonium: V_max = 591.2molg^–1h^–1, K _s=262.3M, nitrate+nitrite: V _max=12.9molg^–1h^–1, K _s=3.5M). Both nutrients were taken up simultaneously, but ammonium incorporation was faster in all cases. The results show a high capability of Ulva rigida to remove sewage-derived nitrogen from culture media. In the field, most of the nitrogen provided by the effluent would be tied up in algal biomass, supporting low nitrogen levels found at a short distance away from the source.     

Untersuchungen zum Polymorphismus der sauren Erythrocytenphosphatasen (E C 3.1.3.2.)

Zusammenfassung Die Bestimmungstechnik der sauren Erythrocytenphosphatasen wird eingehend beschrieben. Untersuchungen zur Formalgenetik bei 80 Familien mit 118 Kindern sowie zur Populationsgenetik und Phylogenetik werden mitgeteilt. Die Ergebnisse widersprechen nicht dem formalen Modell 3 Allele Ph^A, Ph^B, Ph^C an einem autosomalen Locus.

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The method for determination of red cell acid phosphatases is described in detail.Investigations on formal genetics (80 families with 118 children), population genetics and phylogenetics are communicated. The results agree with the assumption: 3 alleles Ph^A, Ph^B, and Ph^C at one autosomal locus.

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Wesentliche Teile dieser Arbeit werden von Fräulein U. Callsen als Dissertation der Medizinischen Fakultät der Universität Freiburg i. Br. vorgelegt.     

Secretion of recombinant human fibrinogen by the murine mammary gland

Transgenic animals secreting individual chains and assembled fibrinogen were produced to evaluate the capacity of the mammary gland for maximizing assembly, glycosylation and secretion of recombinant human fibrinogen (rhfib). Transgenes were constructed from the 4.1kbp murine Whey Acidic Protein promoter (mWAP) and the three cDNAs coding for the A, B and fibrinogen chains. Transgenic mice secreted fully assembled fibrinogen into milk at concentrations between 10 and 200 g/ml, with total secretion of subunits approaching 700 g/ml in milk. Partially purified fibrinogen was shown to form a visible and stable clot after treatment with human thrombin and factor XIII. The level of assembled fibrinogen was proportional to the lowest amount of subunit produced where both the B and chains were rate limiting. Both the B and chains were glycosylated when co-expressed and the degree of saccharide maturation was dependent on expression level, with processing preferred for chains over B chains. Also, the subunit complexes ₂, A₂ and the individual subunits A, B and were found as secretion products. When the B was secreted individually, the glycosylation profile of the molecule was of a mature complex saccharide indicating recognition of the molecule by the glycosylation pathway without association with other fibrinogen chains. To date secretion of B chain has been not observed in any cell type, suggesting that the secretion pathway in mammary epithelia is less restrictive than that occurring in hepatocytes and other cells previously used to study fibrinogen assembly.     

Determination of three enzyme polymorphisms in one electrophoretic step on horizontal polyacrylamide gels

Summary A method that allows separation and determination of three enzyme polymorphisms in one polyacrylamide gel is described. Common phenotypes of adenylate kinase, adenosine deaminase and phosphoglucomutase are diagnosed without difficulties. There are small migration differences between PGM isozymes e and d.

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Zusammenfassung Es wird eine Methode beschrieben, die Trennung und Darstellung von drei Enzympolymorphismen in einem Polyacrylamid-Gel ermöglicht. Die Normtypen der Adenylatkinase, Adenosindeaminase und Phosphoglucomutase sind zweifelsfrei zu differenzieren. Geringe Wanderungsunterschiede ergeben sich zwischen den Zonen e und d der PGM Isoenzyme.

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(Direktor: Prof. Dr. W. Janssen)     

Darstellung und Charakterisierung eines Lipoproteins mit Antigenwirksamkeit im Lp-System

Zusammenfassung Unter Anwendung verfeinerter Trennverfahren wurde das -Lp(a+)-Lipoprotein des menschlichen Serums in immunologisch und elektrophoretisch reiner Form dargestellt. Es wurde hinsichtlich seiner Lipidzusammensetzung analysiert und mit ebenfalls immunologisch und elektrophoretisch rein erhaltenen -Lp(a-)- und ₁-Lipoproteinen verglichen.

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Separation and characterization of a lipoprotein with antigenic activity in the Lp-system

Summary Through application of refined separation techniques the -Lp(a+)-lipoprotein of human serum was characterized in an immunologically and electrophoretically pure form. It was analyzed with regard to its lipid-composition and compared to likewise electrophoretically and immunologically pure -Lp(a-)- and ₁-lipoproteins.

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Untersuchung mit Unterstützung durch die Deutsche Forschungsgemeinschaft     

Paramagnetic spin catalysis of a radical recombination reaction

Recombination of the triplet state radical pair consisting of two hydrogen atoms catalysed by molecular oxygen is considered as a simulating example of a paramagnetic-exchange catalytic process. Intermolecular exchange interaction in the collision complex between the H₂ and O₂ molecules is calculatedab initio in STO-6G and 6–31 G^* basis sets with complete active space configuration interaction. Calculations are done at a fixed O–H distance (3 Å), scanning the H–H bond length from 0.6 till 12 Å at the linear geometry of collision. The mixture of the triplet (T)³ _u ⁺ and singlet (S)¹ _g ⁺ states of the hydrogen moiety is possible because both states have the same triplet symmetry in the collision complex with O₂ (³ _g ^– ). A strong mixture of the S (¹ _g ⁺ , H₂ +³ _g ^– , O₂) and T) and T (³ _u ⁺ , H₂ +³ _g ^– , O₂) states is actually obtained even at large H–H distances. The quintet and singlet states^5,1(³ _u ⁺ , H₂ +³ _g ^– , O₂) are also considered for comparison of the exchange potentials. Atr(H–H)4.4 Å the S-T splitting is approximately constant (12 cm^-1 in the STO-6G basis set; 55.5 cm^-1 in the 6–31 G^* basis set) and is determined by the exchange interaction between O₂ and the nearest hydrogen atom in the O–O...H fragment. The paramagnetic catalyst can accelerate radical recombination through the triplet-singlet nonadiabatic transition to the lowest S reactive state when the radical encounter takes place in the vicinity of the catalyst. Though we do not consider the radical dynamics in a real solvent, which modulates the exchange potentials and the T-S transitions, the nature of this mechanism of spin catalysis is obvious. The electric polarization and charge transfer are important in the analysis of the exchange interaction and radical recombination potentials for all multiplets. In accordance with the concept of spin catalysis, the electronic spin-uncoupling mechanism, induced by O₂ perturbation, has the same nature as other known catalytic processes of paramagnetic-exchange type.     

Optimization of in vivo tumor targeting in SCID mice with divalent forms of 741F8 anti-c-erbB-2 single-chain Fv: effects of dose escalation and repeated i.v. administration

Single-chain Fv molecules in monovalent (sFv) and divalent [(sFv')₂] forms exhibit highly specific tumor targeting in mice as a result of their small size and rapid systemic clearance. As a consequence, there is a rapid reversal of the sFv blood/tumor gradient, resulting in diminished retention of sFv species in tumors. In this report we investigate two distinct strategies, dose escalation and repetitive intravenous (i.v.) dosing, aiming to increase the absolute selective retention of radiolabeled anti-c-erbB-2¹²⁵I-741F8 (sFv')₂ in c-erbB-2-overexpressing SK-OV-3 tumors in mice with severe combined immunodeficiency (SCID). A doseescalation strategy was applied to single i.v. injections of¹²⁵I-741F8 (sFv')₂. Doses from 50 g to 1000 g were administered without a significant decrease in tumor targeting or specificity. High doses resulted in large increases in the absolute retention of¹²⁵I-741F8 (sFv')₂. For example, raising the administered dose from 50 g to 1000 g increased the tumor retention 24 h after injection from 0.46 g/g to 9.5 g/g, and resulted in a net increase of greater than 9 /g. Over the same dose range, the liver retention rose from 0.06 g/g to 1 g/g, and resulted in a net increase of less than 1 g/g. The retention of 9.5 g/g in tumor 24 h fllowing the 1000-g dose of (sFv')₂ was comparable to that seen 24 h after a 50-g dose of¹²⁵I-741F8 IgG, indicating that the use of large doses of (sFv')₂ may partially offset their rapid clearance. When two doses were administered by i.v. injection 24 h apart, the specificity of delivery to tumor observed after the first dose was maintained following the second injection. Tumor retention of¹²⁵I-741F8 (sFv')₂ was 0.32 g/g at 24 h and 0.22 g/g at 48 h following a single injection of 20 g/g, while 0.04 g/ml and 0.03 g/ml were retained in blood at the same assay times. After a second 20-g injection at the 24-h assay time, tumor retention increased to 0.49 g/g, and blood retention was 0.06 g/ml, at the 48-h point. These results suggest that multiple high-dose administrations of radiolabeled 741F8 (sFv')₂ may lead to the selective tumor localization of therapeutic radiation doses.Supported by National Cancer Institute (NCI) National Cooperative Drug Discovery Group grant U01 CA51880, CA06927, an appropriation from the Commonwealth of Pennsylvania, and the Bernard A. and Rebecca S. Bernard Foundation     

Seasonal succession,standing crop and determinants of primary productivity of the phytoplankton of Ministik Lake,Alberta, Canada

Ministik Lake (longitude 113°01; latitude 53°21), a well-mixed, shallow (mean depth 1.83 m), eutrophic lake is characterized by eutrophic chlorococcalean and cyanophycean phytoplankton associations, and little change in standing crop size with increasing depth. Standing crops and primary productivity are low during the winter but pronounced spring and late summer/early autumn maxima occur. Mean yearly areal standing crop (B) and primary productivity (A) were 199.2 mg m^–2 chlorophyll a and 319.5 mg C hr^–1 m^–2 respectively. Annual productivity was estimated at 1399,6 g C m^–2yr^–1. The mean increase in the extinction coefficient () per unit increase in standing crop (B) was 0.03 In units m^–1. High non-algal light attenuation (q) occurred averaging 46% which prevented the ratio B from attaining more than 74.2% of the theoretical maximum except once when selfshading occurred. Insignificant relationships existed between B (mg m^–3 chlorophyll a) and A_max (mg C hr^–1 m^–3), A and B and A and B. Close correlations existed between A and A_max/ and A and I₀ (W m^–2). The depth of the euphotic zone (Z_eu) varied between 0.6 and 2.0 m; the average relationship between z_eu and was z_eu = 3.78/_te, and the mean standing crop in the euphotic zone represented 58.3% of the theoritical maximum. The high _q values made the model of Talling (1957) inapplicable to this lake. The Q₁₀ value for the lake was 1.20. _max (mg C chlorophyll a ^–1 hr^–1) was closely related to both temperature and irradiance, and depressed by high pH values.Growth of the cyanophycean algae was correlated with temperature, chlorophycean algae with phosphate-phosphorus and temperature and the diatoms with dissolved silica and phosphate-phosphorus, but only in the case of Chaetoceros elmorii did any nutrient appear limiting. Indirect evidence that free CO₂ limited photosynthetic rates is provided by the _max:pH relationship.     

Solution to a gene divergence problem under arbitrary stable nucleotide transition probabilities

Summary A nucleic acid chain L nucleotides in length, with the specific base sequence B₁B₂.B_L, each B_i being A, G, C, or T, is defined by the L-dimensional vector B = (B₁, B₂, , B_L), the k^th position in the chain being occupied by the base B_k. Let P_BB' be the twelve given constant non-negative transition probabilities that in a specified position the base B is replaced by the base B in a single step, and let P _BB' ^(XX) be the probability that the position goes from base B to B in X steps. An exact analytical expression for P _BB' ^(XX) is derived. Assuming that each base mutates independently of the others, an exact expression is derived for the probability P _BB' ^(XX) that the initial gene sequence B goes to a sequence B = (B₁, B₂, , B_L) after X = (X₁, X₂, , X_L) base replacements, where X_k is the number of single-step base replacements in the k^th position. The resulting equations allow a more precise accounting for the effects of Darwinian natural selection in molecular evolution than does the idealized but biologically less accurate assumption that each of the four nucleotides is equally likely to mutate to and be fixed as one of the other three. Illustrative applications of the theory to some problems in biological evolution are given.     

Structural characterization of a novel mono-sulfated gangliotriaosylceramide containing a 3-O-sulfatedN-acetylgalactosamine from rat kidney

A novel mono-sulfated glycosphingolipid based on the gangliotriaose core structure was isolated from rat kidney. The isolation procedure involved extraction of lipids with chloroform/methanol, mild alkaline methanolysis, column chromatographies with anion exchangers and silica beads. The structure was characterized by compositional analysis, FTIR spectroscopy, methylation analysis,¹H-NMR spectroscopy and negative-ion liquid secondary ion mass spectrometry (LSIMS) using the intact glycolipid and its desulfation product. The two dimensional chemical shift correlated spectroscopy provided information on the sugar sequence as well as anomeric configurations, and indicated the presence of a 3-O-sulfatedN-acetylgalactosamine within the molecule. Negative-ion LSIMS with high- and low-energy collision-induced dissociation defined the sugar sequence and ceramide composition, confirming the presence of a sulfatedN-acetylgalactosamine at the non-reducing terminus. From these results, the complete structure was proposed to be HSO₃-3GalNAc1-4Gal1-4Glc1-1Cer (Gg₃Cer III³-sulfate, SM2b). Abbreviations: Abbreviations for sulfated glycolipids [17] follow the modifications of the nomenclature system of Svennerholm for gangliosides [37], and the designation of the other glycosphingolipids follows the IUPAC-IUB recommendations [38]. Cer, ceramide; LacCer, lactosylceramide, Gal1-4Glc1-1Cer; Gg₃Cer, gangliotriaosylceramide, GalNAc1-4Gal1-4Glc1-1Cer; Gg₄Cer, gangliotetraosylceramide, Gal1-3GalNAc1-4Gal1-4Glc1-1Cer; iGb₄Cer, isoglobotetraosylceramide, GalNAc1-3Gal1-3Gal1-4Glc1-1Cer; Gb₄Cer, globotetraosylceramide, GalNAc1-3Gal1-4Gal1-4Glc1-1Cer; SM4s, galactosylceramide sulfate, GalCer I³-sulfate; SM3, lactosylceramide sulfate, LacCer II³-sulfate; SM2a, Gg₃Cer II³-sulfate; SM2b, Gg₃Cer III³-sulfate; SB2, Gg₃Cer II³,III³-bis-sulfate; SM1a, Gg₄Cer II³-sulfate; SM1b, Gg₄Cer IV³-sulfate; SB1a, Gg₄Cer II³,IV³-bissulfate; GLC, gas-liquid chromatography; GC-MS, gas chromatography-mass spectrometry; DQF, double quantum filtered; COSY, chemical-shift-correlated spectroscopy; LSIMS, liquid secondary ion mass spectrometry; CID, collision-induced dissociation; MS/MS, tandem mass spectrometry.     

Spectral hole burning of the primary electron donor state of Photosystem I

Persistent photochemical hole burned profiles are reported for the primary electron donor state P700 of the reaction center of PS I. The hole profiles at 1.6 K for a wide range of burn wavelengths (_B) are broad (FWHM310 cm^-1) and for the 45:1 enriched particles studied exhibit no sharp zero-phonon hole feature coincident with _B. The _B hole profiles are analyzed using the theory of Hayes et al. [J Phys Chem 1986, 90: 4928] for hole burning in the presence of arbitrarily strong linear electron-phonon coupling. A Huang-Rhys factor S in the range 4–6 and a corresponding mean phonon frequency in the range 35–50 cm^-1 together with an inhomogeneous line broadening of100 cm^-1 are found to provide good agreement with experiment. The zero-point level of P700^* is predicted to lie at710 nm at 1.6K with an absorption maximum at702 nm. The hole spectra are discussed in the context of the hole spectra for the primary electron donor states of PS II and purple bacteria.Abbreviations NPHB nonphotochemical hole burning - O.D. optical density - PSBH phonon sideband hole - PS I Photosystem I P680 - P700, P870, P960 the primary electron donors of Photosystem II, Photosystem I, Rhodobacter sphaeroides, Rhodopseudomonas viridis - PED primary electron donor - RC reaction center - ZPH zero-phonon holes     

The photosynthetic F1-α3β3 and α1β1 catalytic core complexes

Minimal photosynthetic catalytic F₁() core complexes, containing equimolar ratios of the and subunits, were isolated from membrane-bound spinach chloroplast CF₁ and Rhodospirillum rubrum chromatophore RrF₁. A CF₁-₃₃ hexamer and RrF₁-₁₁ dimer, which were purified from the respective F₁() complexes, exhibit lower rates and different properties from their parent F₁-ATPases. Most interesting is their complete resistance to inhibition by the general F₁ inhibitor azide and the specific CF₁ inhibitor tentoxin. These inhibitors were earlier reported to inhibit multisite, but not unisite, catalysis in all sensitive F₁-ATPases and were therefore suggested to block catalytic site cooperativity. The absence of this typical property of all F₁-ATPases in the ₁₁ dimer is consistant with the view that the dimer contains only a single catalytic site. The ₃₃ hexamer contains however all F₁ catalytic sites. Therefore the observation that CF₁-₃₃ can bind tentoxin and is stimulated by it suggests that the F₁ subunit, which is required for obtaining inhibition by tentoxin as well as azide, plays an important role in the cooperative interactions between the F₁-catalytic sites.Abbreviations CF₀F₁ chloroplast F₀F₁ - CF₁ chloroplast F₁ - CF₁ chloroplast F₁ subunit - CF₁ chloroplast F₁ subunit - CF₁() a complex containing equal amounts of the CF₁ and subunits - MF₁ mitochondrial F₁ - RrF₀F₁ Rhodospirillum rubrum F₀F₁ - RrF₁ R. rubrum F₁ - RrF₁ R. rubrum F₁ subunit - RrF₁ R. rubrum F₁ subunit - RrF₁() a complex containing equal amounts of the RrF₁ and subunits - Rubisco Ribulose-1,5-bisphosphate carboxylase - TF₁ thermophilic bacterium PS3 F₁     

Synthèse d'ARN et de protéines dans des disques de patte de drosophile cultivés in vitro

Résumé Des disques imaginaux de patte, prélevés dans des larves de fin de 3e stade de drosophile, ont été cultivés dans le milieu M de Mandaron, en l'absence d'hormone ou en présence soit d'- soit de -ecdysone. L'incorporation de précurseurs marqués (³H-uridine,³H-leucine ou³H-proline) a été étudiée en fonction du stade de développement des disques.En l'absence d'hormone de mue, l'incorporation d'uridine décroît dès que les disques ont été explantés; l'incorporation de leucine et de proline ne décroît que 6 à 12 heures après l'explantation.- et -ecdysone stimulent l'incorporation des trois précurseurs; toutefois celle-ci varie en fonction du développement morphologique du disque.Les maxima et les minima d'incorporation d'uridine précèdent dans le temps ceux de la leucine et de la proline.Les maxima d'incorporation peuvent être mis en rapport avec des évènements morphologiques marquants du développement: évagination, sécrétion des cuticules nymphale et maginale.Il n'y a pas de différences significatives d'incorporation d'uridine en présence d'-ecdysone ou de -ecdysone; en revanche les maxima d'incorporation de leucine et de proline sont plus élevés en présence d'-ecdysone que de -ecdysone.Ces résultats montrent que l'-ecdysone—et à un degré moindre la -ecdysone—peuvent induire les synthèses de macromolécules nécessaires au développement des appendices in vitro.

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RNA and protein synthesis inDrosophila leg discs cultured in vitro

Summary Imaginal leg discs from late third instarDrosophila larvae were cultured in Mandaron's medium without hormone or with -ecdysone or -ecdysone. Incorporation of labelled precursors (tritiated uridine, tritiated leucine or tritiated proline) was studied as a function of the stage of in vitro disc development.In the absence of moulting hormone, uridine incorporation decreased as soon as the discs were explanted; leucine and proline incorporation however began to decrease only after 6 to 12 h.- and -ecdysone stimulated the incorporation of all three precursors; however the rate of the incorporation varied as a function of the morphological disc development.The maxima and minima of uridine incorporation preceeded in time those of proline and leucine incorporation.The peaks of incorporation were coincident with salient morphological events of development: evagination, secretion of pupal and imaginal cuticles.There were no significant differences in uridine incorporation in the presence of -ecdysone or -ecdysone. Leucine and proline incorporation maxima however were significantly higher in the presence of -ecdysone than of -ecdysone.The results show that -ecdysone—and to a lesser extent also -ecdysone—can induce the macromolecular syntheses required for the development of the appendage in vitro.

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Ce travail a été réalisé avec l'aide du CNRS (Action thématique programmée «Différenciation cellulaire», contrat n^o A 6554324)

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Ce mémoire représente une partie de la thèse qui sera soutenue par l'auteur devant l'Université Scientifique et Médicale de Grenoble     

Light-oriented locomotion in certain myxobacter species

Summary Euglena gracilis, strain Z, was grown in synchronous culture. Carbon source used was either dl-lactic acid (L) or a mixture of l-glutamic and dl-malic acids (GM). Synchronisation was obtained by transfering the cells in the exponential growth phase, at regular intervals—each 3 days—to a fresh medium.Respiration (measured during a whole cell cycle, 12 h) was 20±6 l/H/10⁶ cells on (GM) and 46±7 l/H/10⁶ cells on (L) medium. At the same time as the increased rate of oxygen uptake on lactate medium, we observed the appearance of a giant chondriome in the cells. On glutamate—malate containing medium the size of mitochondria was normal.

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Les micrographies électroniques ont été réalisées par Mr. C. Mattei, Technicien CNRS.     

Product inhibition during the feeding phasein fed-batch ethanol fermentation of sugar-cane blackstrap molasses

Summary The following equations represent the influence of the ethanol concentration (E) on the specific growth rate of the yeast cells () and on the specific production rate of ethanol () during the reactor filling phase in fed-batch fermentation of sugar-cane blackstrap molasses: = ₀ - k · E and v = v ₀ · K/(K +E) Nomenclature E ethanol concentration in the aqueous phase of the fermenting medium (g.L^–1) - E_m value of E when = 0 or = 0 (g.L^–1) - F medium feeding rate (L.h^–1) - k empirical constant (L.g^–1.h^–1) - K empirical constant (g.L^–1) - M_as mass of TRS added to the, reactor (g) - M_cs mass of consumed TRS (g) - M_e mass of ethanol in the aqueous phase of the fermenting medium (g) - M_s mass of TRS in the aqueous phase of the fermenting medium (g) - M_x mass of yeast cells (dry matter) in the fermenting medium (g) - r correlation coefficient - S TRS concentration in the aqueous phase of the fermenting medium (g.L^–1) - S_m TRS concentration of the feeding medium (g.L^–1) - t time (h) - T temperature (° C) - TRS total reducing sugars calculated as glucose - V volume of the fermenting medium (L) - V₀ volume of the inoculum (L) - X yeast cells concentration (dry matter) in the fermenting medium (g.L^–1) - filling-up time (h) - specific growth rate of the yeast cells (h^–1) - ₀ value of when E=0 - specific production rate of ethanol (h^–1) - ₀ value of when E=0 - density of the yeast cells (g.L^–1) - dry matter content of the yeast cells     

De novo induction of adventitious roots in excised shoots of tomatoes by fumonisin B1, a metabolite of Fusarium moniliforme

The de novo induction of roots in tomatoes (Lycopersicon esculentum) Mill. cvs. Earlypak-7, Ace, Better Boy, Roma, and Parks' Whopper by fumonisin B₁, a mycotoxin produced by Fusarium moniliforme J. Sheld., was studied. In graded dosages of fumonisin B₁, detached stems of the cultivars Ace, Better Boy, and Roma were induced to produce calluses and roots earlier than controls. The cultivar Ace was especially responsive to this mycotoxin, and following a single application, callus initiation was observed to occur within a 24–48-h period and roots were produced as early as 72 h with 10 g/shoot or as late as 96 h with low dosages. The control plants of all cultivars were completely negative for a rooting response during this time. Some cultivars treated with fumonisin B₁ showed either no response or developed signs of phytotoxicity. Those cultivars that were stimulated to produce roots did not show signs of phytotoxicity, except at dosages of 0.5 mg/plant and higher. One cultivar did not show any signs of phytotoxicity nor was it induced to root. The ability of fumonisin B₁ to affect the accumulation of calcium in other systems, and its structural similarity to sphingosine suggest that the induction of adventitious roots may be a calcium-dependent process.     

UV-Sehfarbstoff bei Insekten

Summary From insect eyes, an u.v.-visual pigment A (_max 345 nm) was extracted by 2% aqueous digitonin (pH 5.2). Upon prolonged u. v. irradiation, A is converted to a stable product B (_max 480 nm), which reconverts completely to A when illuminated with light of longer wavelengths. When the pH of B is raised to 9.3, B is converted to C and absorbs at 375 nm. Experiments with NH₂OH lead us to the assumption that retinal is the prosthetic group of this pigment.

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Die Arbeit wurde durch jugoslawische SBK- und SFNR-Fonds gefördert. K. Hamdorf und J. Schwemer danken der Deutschen Forschungsgemeinschaft für großzügige Unterstützung.     

Light and GTP dependence of transducin solubility in retinal rods

The physical origin and functional significance of the near infra-red light scattering changes observable upon flash illumination of diluted suspensions of magnetically oriented, permeabilised frog retinal rods has been reinvestigated with particular attention paid to the degree with which transducin remains attached to the membrane. In the absence of GTP, the so called binding signal is shown to include two components of distinctive origins, widely different kinetics, and whose relative amplitudes depend on the dilution of the suspension and resulting detachment of transducin from the disc membrane. The fast component is a consequence of the fast interaction between photoexcited rhodopsin (R^*) and the transducin remaining on the membrane. Its kinetics monitors a structural modification of the discs caused by a change in electrostatic interaction between closely packed membranes upon the formation of R^*-T complexes. The slow component monitors the slow rebinding to the membrane and possible subsequent interaction with excess R^* of T-GDP which, in spite of its low solubility, had eluted into solution given the high dilution of the permeated rods. In the presence of GTP, the so called dissociation signal includes a fast, anisotropic release component that specifically monitors the release into the interdiscal space of T -GTP formed from the membrane-bound pool, and a slower isotropic loss component monitoring the leakage from the permeated rod of the excess T -GTP which did not interact with the cGMP phosphodiesterase. The amplitudes of both components depend exclusively on the membrane bound T-GDP pool. The kinetics of the loss component is limited by the size and degree of permeation of the rod fragments, rather than by the dissociation rate of T -GTP from the membrane.Abbreviations ROS rod outer segment - R rhodopsin - R^* photoactivated rhodopsin - T, T-GDP, T -GDP, T -GTP, T transducin and its various forms - T _mb, T _sol: T bound to membrane or soluble - PDE cGMP-phosphodiesterase - GTP guanosine 5-triphosphate - GDP guanosine 5-diphosphate - GDP S guanosine 5-O-(2-thiodiphosphate) - cGMP guanosine-3-5 cyclic-monophosphate - DTT dithiothreitol - HEPES 4-(2-hydroxyethyl)-1-piperazine-ethane sulfonic acid - TRIS Tris (hydroxymethyl)aminomethane - SDS sodium dodecyl sulfate     

Existence and uniqueness of a sharp travelling wave in degenerate non-linear diffusion Fisher-KPP equations

In this paper we use a dynamical systems approach to prove the existence of a unique critical value c ^* of the speed c for which the degenerate density-dependent diffusion equation u _ct = [D(u)u _x ] _x + g(u) has: 1. no travelling wave solutions for 0 < c < c ^*, 2. a travelling wave solution u(x, t) = (x - c ^* t) of sharp type satisfying (– ) = 1, () = 0 ^*; '(^*–) = – c ^*/D'(0), '(^*+) = 0 and 3. a continuum of travelling wave solutions of monotone decreasing front type for each c > c ^*. These fronts satisfy the boundary conditions (– ) = 1, '(– ) = (+ ) = '(+ ) = 0. We illustrate our analytical results with some numerical solutions.