The analogs of oxytocin and D-homoarginine vasopressin with bulky substituted phenylalanine in position 2

Summary Solid phase technique on p-methylbenzhydrylamine resin was used for the synthesis of eight analogs of oxytocin and 8-D-homoarginine vasopressin with the non-coded amino acids L- or D-2,3,4,5,6-pentamethylphenylalanine and L- or D-4-phenylphenylalanine in position 2. The preparation of the above mentioned non-coded amino acids is described as well. All eight analogs were found to be potent inhibitors of oxytocin activity in the uterotonicin vitro test in the absence of Mg²⁺ ions. In the uterotonic testin vitro in the presence of Mg²⁺ and in the testin vivo, their potency is strongly decreased or completely abolished. The substances are also weak pressor inhibitors. The L or D configuration does not seem to influence the activity significantly. Abbreviations: All the chiral amino acids unless otherwise stated are of the L-series. Phe(4-Ph) denotes the 4-phenylphenylalanine, Phe(pentaMe) the 2,3,4,5,6-pentamethylphenylalanine, Har the homoarginine, DMF dimethylformamide, OHBT 1-hydroxybenzotriazole and DCC dicylohexyl-carbodiimitz. The Nomenclature and symbols of the amino acids and peptides obey the published recommendations: IUPAC-IUB Joint Commission on Biochemical Nomenclature: Eur. J. Biochem., 138 (1984) 9.     

Some evidence confirming the specificity of Barrnett and Seligman's technique for demonstrating side-chain carboxyl groups in proteins

Summary There is some confusion in the literature as to whether the protein carboxyl groups demonstrable with Barrnett and Seligman's histochemical technique are C-terminal or side-chain. It seems that in the first step of this technique, hot mixtures of acetic anhydride and pyridine convert the commonly-occurring side-chain carboxyls into mixed acid anhydrides. That they do has now been confirmed; proteins in tissue sections treated with such acetic anhydride mixtures do not react with hydroxynaphthoic acid hydrazide after being left for a long time in either cold methanol or a cold solution of aniline in xylene. In this they resemble the acid anhydrides used for synthezising peptides in vitro. Thus all the lilac-reddish colours observable in tissue proteins on which the Barrnett and Seligman technique proper has been carried out can be ascribed to side-chain carboxyl groups.     

The analogs of oxytocin and D-homoarginine vasopressin with bulky substituted phenylalanine in position 2

Solid phase technique on p-methylbenzhydrylamine resin wasused for the synthesis of eight analogs of oxytocin and 8-D-homoarginine vasopressin with the non-coded amino acids L- or D-2,3,4,5,6-pentamethylphenylalanine and L- or D-4-phenylphenylalanine in position 2. The preparation of theabove mentioned non-coded amino acids is described as well.All eight analogs were found to be potent inhibitors ofoxytocin activity in the uterotonic in vitro test in theabsence of Mg²⁺ ions. In the uterotonic test invitro in the presence of Mg²⁺ and in the test invivo, their potency is strongly decreased or completelyabolished. The substances are also weak pressor inhibitors.The L or D configuration does not seem to influence theactivity significantly.     

<Emphasis Type="Italic">In vitro</Emphasis> propagation and cryostorage of <Emphasis Type="Italic">Syzygium francissi (Myrtaceae)</Emphasis> by the encapsulation-dehydration method

Summary An efficient procedure for the in vitro propagation and cryogenic conservation of Syzygium francissi was developed. The maximum number of shoots per explant was obtained on a Murashige and Skoog (MS) medium supplemented with 4.5 μM benzyladenine and 0.5 μM indole-3-butyric acid (IBA). The in vitro-propagated shoots produced roots when transferred to MS medium containing IBA, indold-3-acetic acid, or naphthaleneacetic acid at various concentrations. Rooted microshoots were transferred to a coco-peat, perlite, and vermiculite (1∶1∶1) mixture, and hardened off under greenhouse conditions. Ninety-five percent of rooted shoots successfully acclimatized in the greenhouse. Shoot tips excised from in vitro-grown plants were successfully cryostoraged at −196°C by the encapsulation-dehydration method. A preculture of formed beads on MS medium containing 0.75 M sucrose for 1 d, followed by 6 h dehydration (20% moisture content) led to the highest survival rate after cryostorage for 1h. This method is a promising technique for in vitro propagation and cryopreservation of shoot tips from in vitro-grown plantlets of S. francissi germplasm.     

Antigenic characterization of Nephrops norvegicus (L.) hepatopancreas cells

During this work structural, differentiation and proliferation antigenic markers developed for mammals were applied in paraffin sections of Nephrops norvegicus (L.) hepatopancreas. The purpose was to establish standards for the characterization of invertebrate cells in vitro. Antibody concentration was optimized for quantification of cell proliferation. There are no antibodies specific for crustaceans on the market. An avidin–biotin immunoperoxidase method was used to visualize cell antigen expression. The immunocytochemical results indicate that the epithelium in the Nephrops hepatopancreas digestive tubules does express cytokeratins and proliferating cell nuclear antigen. The results of this work indicate that some mammalian antibodies cross‐react with crustacean epitopes. This may facilitate cell characterization of cell types cultured in vitro. Copyright © 1999 John Wiley & Sons, Ltd.     

Effects of conformational constraint in 2- and 8-cycloleucine analogues of oxytocin and [1-penicillamine] oxytocin examined by circular dichroism and biosassay

The analogues of oxytocin and [1-penicillamine]oxytocin, containing a cycloleucine (Cle) residue in position 2 or 8, were investigated by means of circular dichroism measurements in different solvents, and the results examined in terms of their biological activities. A cycloleucine residue in position 2 substantially reduces the free conformational space of the hormone 20-membered ring moiety (including the disulfide group), and stabilizes a conformation which is close to one of the possible conformations of oxytocin and involves a -turn. In position 8, the Cle residue affects the conformation of the Tyr² side chain, apparently forcing it away from the space above the 20-membered disulfide ring. However, it does not appear that the Cle residue has any significant effect on the overall backbone conformation of the hormone. The steric effect of the penicillamine residue in position 1 on the conformation of the disulfide group and Tyr² side chain from previous investigations is further confirmed. The synthesis and biological potency of [1-penicillamine, 8-cycloleucine]oxytocin is described. This analogue exhibits a strong inhibitory effect on the uterotonic activity of oxytocinin vitro. It also inhibited the vasopressor response to vasopressin.     

Development of an in vitro incubation technique for the estimation of the utilizable crude protein (uCP) in feeds for cattle

An in vitro incubation technique based on the first stage of the in vitro digestion technique published by Tilley and Terry (1963) was developed to estimate the utilizable crude protein (uCP) of single feeds and feed mixtures as non ammonia‐N after 24 h of incubation. The results of 25 feed samples showed that there was a significant relationship between the uCP values calculated by regression based on in vivo data sets (Y, CP [g‐kg^‐1 DM]) and those measured by the in vitro incubation technique (X, CP [g‐kg^‐1 DM], 24 h incubation):

y=0.85x+18.0, r²=0.84, P≤0.001.

It was concluded that it can be possible to determine the uCP value of single feeds or feed mixtures by this in vitro incubation technique and to estimate the uCP value of feeds by this regression equation.     

Direct somatic embryogenesis and shoot regeneration from leaves and internodes of Pluchea lanceolata (DC.) C.B. Clarke

Pluchea lanceolata (DC.) C.B. Clarke is a threatened native medicinal plant. Increasing the propagation of this plant will preserve the wild population and provide material for medicinal use. In vitro and field-collected shoots and leaves were tested for response to 2,4-dichlorophenoxyacetic acid (2,4-D) and thidiazuron (TDZ), for initiation of direct shoot regeneration (DSR), or direct somatic embryogenesis (DSE). Leaves and internodes collected from field-grown plants produced only callus, while in vitro–raised shoots exhibited DSR and DSE on Murashige and Skoog (MS) medium with 2,4-D and TDZ. Direct shoot regeneration occurred on medium with TDZ from internode and leaf segments obtained from in vitro–developed shoots. In vitro–grown shoots were rooted on half-strength MS medium with 2 mg L⁻¹ indole-3-butyric acid and acclimatized. Survival in natural conditions was 62.5% for DSE and 79% for DSR plantlets.

     

In vitro propagation of Spilanthes mauritiana DC., an endangered medicinal herb, through axillary bud cultures

Summary Spilanthes mauritiana DC., (Compositae), a East African medicinal herb containing pharmaceutically promising secondary metabolites, has successfully been raised in vitro. We have developed a clonal propagation protocol that uses juvenile plants as starting material. The addition of benzylaminopurine (BA) (1.0 μM) and naphthaleneacetic acid (NAA) (0.1 μM) to the culture medium resulted in maximum shooting response with minimal callusing. Shoots rooted best in vitro in MS medium supplemented with indole-3-acetic acid (IAA; 0.2 μM), and plants that had already developed roots showed better growth, with maximum survival rate, in the greenhouse after an initial hardening.     

Detection of Pseudocercosporella herpotrichoides (Fron) Deighton in Wheat by Indirect ELISA

An indirect ELISA for quantitative detection of P. herpotrichoides in fections in wheat is presented. All tested isolates of the virulent varieties P. herpotrichoides var. herpotrichoides, P. h. var. acuformis or the W- and R-type react on a high level in the test, while the less virulent P. anguioides is assessed only with 40% and the avirulent P. aestiva with 20% of the homologous reaction. No crossreactions occur with extracts of 11 other species of in, vitro cultivated fungi nor with plant material infected with other pathogens. The infection profile throughout the leaf-sheaths was clearly reflected by ELISA. The examination of 24 stembase samples from the field showed that the values assessed by ELISA correlate well also with the disease indices of naturally infected plant material.     

The "prostaglandin step", a bottleneck in the activation of the uterus

Uterine strips were excised from post partum rabbits, mounted $\text{in vitro}$ and stimulated electrically to sustain cyclic tension at a maximal value. Within 10–15 minutes after exposure to 1.5–2.0 mg/ml Naproxen (a derivative of propionic acid and an inhibitor of PG-synthesis) uterine tension decreased to less than 25% of the original value. The effect of Naproxen (N), also observed in spontaneously active (unstimulated) uteri, was suspended by removing N through washing the strips with mammalian Krebs' solution.When suppressed by N, uterine tension could be restored by exogenous PG F2α but not by oxytocin, in spite of a 1000 fold increase in that oxytocin concentration which effectively stimulated the normal uterus (unexposed to N). This failure of oxytocin in promoting activation, when the PG-synthesis of the uterus was blocked, suggest that endogenous PGs participate in a critical step of the sequence of events which provoke myometrial activity.     

THE PAS/ACCUMULATION BODIES IN PROROCENTRUM LIMA AND PROROCENTRUM MACULOSUM (DINOPHYCEAE) ARE DINOFLAGELLATE LYSOSOMES1

Numerous spherical bodies containing electron-dense material, fibrous material, and membranous material are present in the cytoplasm of two dinoflagellate species, Prorocentrum lima (Ehr.) Dodge and Prorocentrum maculosum Faust. Similar bodies have been observed in other dinoflagellates and have been termed accumulation bodies or PAS bodies. In both Prorocentrum species, these bodies autofluoresce under blue light excitation and increase in size with cell culture age. They possess acid phosphatase activity, react positively with the periodic acid/Schiff reagent, and stain with acridine orange. All these properties are characteristic of eukaryotic lysosomes; thus, we propose that dinoflagellate accumulation bodies and PAS bodies are identical organelles and are, in fact, dinoflagellate lysosomes.     

In vitro propagation of Notocactus magnificus

Most commercially grown cacti can be easily propagated by seed and/or cuttings. A group of rare and endangered species does not fit into this category and is therefore a good candidate for in vitro propagation productions as a tool to overcome habitat and plant-destruction. The number of rare and endangered species of Cacti goes into about 100. Many show a low production and germination of seeds and plantlets are prone to damping-off, making the in vitro propagation a feasible alternative for the multiplication and conservation of their germplasm. The aim of the present investigation is to establish a protocol for the in vitro culture and plant regeneration of Notocactus magnificus, the blue cactus, a highly ornamental species, native to Brazil. The surface sterilization of the explants was achieved with immersion for 10 min in sodium hypochlorite solution for either seeds (0.25% v/v) or ribs segments (1% v/v). Callus formation was observed when explants were cultured on MS medium supplemented with sucrose at 2% (w/v), 2,4-dichlorophenoxyacetic acid 0.5 μM, benzylaminopurine 4.4 μM, thiamine HCl 0.4 mg l⁻¹ and i-inositol 100 mg l⁻¹. The regeneration of shoots was carried out on MS medium supplemented with either different concentrations of benzylaminopurine and 1-naphthaleneacetic acid, or kinetin and indole-3-acetic acid. The highest number of shoots occurred when MS medium was supplemented with benzylaminopurine 22.2 μM, sucrose 3% (w/v) and agar 0,6% (w/v). In vitro spontaneous rooting of shoots was observed after eight months under culture on MS medium. Only in vitro rooted shoots developed into normal plants under glasshouse culture conditions. This in vitro protocol should be useful for the conservation as well as mass propagation of Notocactus magnificus.     

In vitro rescue of isolated embryos of Bactris major jacq. and Desmoncus orthacanthos mart., potentially useful native palms from the Yucatan Peninsula (Mexico)

Summary Bactris major and Desmoncus orthacanthos are native palms from the Yucatan Peninsula which could be used as substitutes for rattan. When their seeds were germinated in vivo and in vitro they proved to be highly recalcitrant. Therefore, the culture of isolated embryos was studied as an alternative means of producing planting material for nurseries. It was found that the in vitro germination of the isolated embryos was gradually reduced by storage, falling to zero by 5 wk. However, isolated embryos from freshly collected seeds germinated at ∼100% frequency. The presence of the endosperm, whether still attached to the embryos or separated from them but in direct contact with the nutrient medium, greatly reduced germination in both species. High concentrations of abscisic acid (ABA, 100 μM) only slightly diminished it, suggesting a different cause for the observed endosperm-induced inhibition. This embryo rescue method permits the production of sufficient plants for in vitro micropropagation and the establishment of experimental plots to evaluate the full potential of these materials.     

Regeneration capacity of selected genotypes of white mustard (Sinapis alba L.)

Traditional breeding methods based on inbreeding are difficult to implement in the case of Sinapis alba (white mustard) because this plant displays high levels of self-incompatibility. More rapid progress in breeding could be possible if biotechnological methods and in vitro cultures were used. However, white mustard is not readily amenable to biotechnological treatment. Seeds of traditional S. alba cultivars (e.g., Nakielska) are characterized by high levels of glucosinolates and erucic acid. However, a new Polish variety of white mustard (Bamberka) possesses low erucic acid content in the oil. The main goal of the study was elaboration of a plant regeneration system via in vitro culture of hypocotyl and cotyledon explants from low and high erucic acid-containing white mustard cultivars. In these experiments, a simple system for in vitro regeneration of white mustard was developed, with the aim to promote maximum formation of shoots within a short period of time. Traditional and improved cultivars of S. alba showed comparable capacity for shoot development from hypocotyl-derived and cotyledon-derived explants. The two types of cultivars were characterized by essentially equivalent shoot regeneration responses, being slightly higher in hypocotyl than the cotyledonary explants. A greater influence on shoot regeneration from hypocotyl explants was observed on medium supplemented with 4.4 μmol 6-benzylaminopurine, 0.57 μmol indole-3-acetic acid, and a low concentration of kinetin (4.6 μmol). This technique will allow for rapid generation of sufficient plant material for further use in a variety of white mustard breeding projects.     

Inactivation of Bacillus cereus by Na‐chlorophyllin‐based photosensitization on the surface of packaging

Aims: This study was focused on the possibility to inactivate food‐borne pathogen Bacillus cereus by Na‐chlorophyllin (Na‐Chl)‐based photosensitization in vitro and after attachment to the surface of packaging material. Methods and Results: Bacillus cereus in vitro or attached to the packaging was incubated with Na‐Chl (7·5 × 10^?8 to 7·5 × 10^?5 mol l^?1) for 2–60 min in phosphate buffer saline. Photosensitization was performed by illuminating cells under a light with a λ of 400 nm and an energy density of 20 mW cm^?2. The illumination time varied 0–5 min and subsequently the total energy dose was 0–6 J cm^?2. The results show that B. cereus vegetative cells in vitro or attached to the surface of packaging after incubation with 7·5 × 10^?7 mol l^?1 Na‐Chl and following illumination were inactivated by 7 log. The photoinactivation of B. cereus spores in vitro by 4 log required higher (7·5 × 10^?6 mol l^?1) Na‐Chl concentration. Decontamination of packaging material from attached spores by photosensitization reached 5 log at 7·5 × 10^?5 mol l^?1 Na‐Chl concentration. Comparative analysis of different packaging decontamination treatments indicates that washing with water can diminish pathogen population on the surface by <1 log, 100 ppm Na‐hypochlorite reduces the pathogens about 1·7 log and 200 ppm Na‐hypochlorite by 2·2 log. Meanwhile, Na‐Chl‐based photosensitization reduces bacteria on the surface by 4·2 orders of magnitude. Conclusions: Food‐borne pathogen B. cereus could be effectively inactivated (7 log) by Na‐Chl‐based photosensitization in vitro and on the surface of packaging material. Spores are more resistant than vegetative cells to photosensitization‐based inactivation. Comparison of different surface decontamination treatments indicates that Na‐Chl‐based photosensitization is much more effective antibacterial tool than washing with water or 200 ppm Na‐hypochlorite. Significance and Impact of the Study: Our data support the idea that Na‐Chl‐based photosensitization has great potential for future application as an environment‐friendly, nonthermal surface decontamination technique.     

An Improvement in the Sensitivity of the Salkowski Reagent for Tryptamine, Tryptophan and Indoleacetic Acid

The reaction of indoles with the Salkowski reagent has been examined. It was found that the concentration of acid as well as the concentration and anionic component of the iron salt employed are critical factors in the choice of a reagent that will fail to react—or will react maximally with a given indole. Tryptamine can be reproducibly assayed with a reagent containing 0.01 M Fe(NO₃)₃ in 7.0 M HCIO₄. Two ml of this reagent are added to two ml of the sample. The absorbancy is read at 450 nm after 90 minutes under uniform light conditions. Versions of this reagent can also be used for the quantitative colorimetric determination of tryptophan or indoleacetic acid.     

Transfer Agent of Immunity

Antibody formation in vitro was studied using erythrocytes (RBC) as antigen and immunocytoadhesion as the technique for detection of antibody-forming cells. Spleen cells (SPC) of nonimmune mice gained the ability to produce antibody after treatment with ribonucleic acid (RNA) preparation extracted from allogeneic mice immunized with xenogeneic or allogeneic RBC. It was also found that a small proportion of SPC from individual mice of certain strains formed antibody against autologous RBC when the cells were treated in vitro with RNA preparation obtained from the spleen of an allogeneic mouse immunized with RBC of that individual. No converting ability was observed in the RNA preparation from spleen of nonimmune autologous or allogeneic mice. The converting activity of immune RNA preparation was shown to be sensitive to ribonuclease treatment. These evidences exclude the possible contribution of antigen or fragments thereof in the RNA preparation to the induction of antibody formation in RNA recipient cells.     

Morphogenetic sequences of the rooting process after in vitro culture or Agrobacterium rhizogenes inoculation

Abstract

After a brief review dealing with the factors inducing adventitious rhizogenesis, the morphogenetic patterns of the rooting process induced by in vitro culture or after Agrobacterium rhizogenes inoculations are described. In vitro cultures of Nicotiana tabacum, Datura innoxia and Crepis capillaris leaf explants on Murashige and Skoog's medium supplemented with sucrose and IAA or NAA have been used in order to identify the target cells for direct and indirect rooting. The structural and functional features of the prerhizogenetic cells are described and the ploidy levels of both direct and indirect root meristems are examined by means of DNA microspectrophotometry. Data on the synergistic effects between auxin, sucrose and amino acids (particularly L-ornithine) for the reactivation of the prerhizogenetic cells are also given.

Transformed roots from carrct root discs or pea epicotyls after Agrobacterium rhizogenes inoculation arise indirectly from cambium-like layers differentiated inside a previously formed callus. Numerous auxin-like symptoms at the cell level are detected after the inoculation, suggesting modifications in the endogenous contents of auxin prior to the rooting process. It is also shown that initially non-susceptible cells (fully differentiated tobacco pith) can be induced to become susceptible by in vitro treatments resulting in cell reactivation before inoculation with the bacteria. Further work is in progress to extend these observations to non-susceptible species in order to check, via the occurrence of transformed roots, their ability to react positively to foreign Ri T-DNA.     

A Comparison of the Disease Reactions of Stems and Detached Leaves of Soil and in vitro Grown Plants and Regenerants of Oilseed Rape to Leptosphaeria maculans and Protocols for Selection for Novel Disease Resistance

Protocols for selecting plant tissues of winter oilseed rape (Brassica napus subsp. oleifera) with resistance to Leptosphaeria maculans by either stem or leaf inoculation of both soil and in vitro grown plant material are described. The stem inoculation procedure gave good correlation (r = 0. 92) between the 50 day stem disease scores of eight out of nine cultivars of soil grown winter oilseed rape inoculated with isolate 41A4 of L. maculans and the N. A. B. esistance ratings or resistance data from field trials. The exception was the cultivar Liradonna. Inoculation of stems of five cultivars with isolates 41A4, 433 and 478 indicated a range of isolate virulence 478 > 41A4 > 433. This was the inverse of that observed in leaf inoculations. Application of the stem inoculation procedure to in vitro shoot cultures allowed differentiation of resistant and susceptible cultivars, including the cultivar Liradonna, after 20 days incubation at 20°C. The protocol was also applicable to plantlets regenerated from thin cell layer explants grown in vitro. Inoculations with isolate 433 allowed the differentiation of resistant, intermediately resistant and susceptible leaf material of soil grown plants, when leaf discs from young leaves were incubated on water agar supplemented with BAP (1 × 10^?5 M) at 25°C for 10 days. Intermediately resistant leaves were resistant after 10 days and susceptible after 15 days of incubation. Leaves of shoot cultures grown in vitro were more susceptible than the corresponding soil grown material. However, inoculation of old leaves with isolate 41A4 (an isolate of less virulence on leaves than 433) distinguished the cultivars after 15 days of incubation. These protocols allow the accurate assessment of resistance to L. maculans at the stem or leaf level and are of use in traditional as well as in vitro selection programmes.