Influence of Nitrogen Supply of Potato Plantlets on In Vitro Tuberization Pattern under Inductive and Non-inductive Conditions

The effects of nitrogen supply of in vitro plantlets on subsequent in vitro tuberization were examined in three potato varieties. In vitro plantlets were raised on MS media with varying amounts of ammonium nitrate, resulting in 70, 80, 100, 120 and 160% of the standard N content in MS medium and various nitrate : ammonium ratios. Tuberization was induced by adding an 8% sucrose solution to 4-week old plantlets and keeping them 2 weeks under short or long days (8 and 16 h illumination per day, respectively), followed by darkness for 9 weeks. Under long days, a lower nitrogen content in the medium and higher nitrate : ammonium ratio were favourable for the development of large tubers (>6 mm). Under short days, the total number of tubers increased with an increase in nitrogen content of the medium in cultivars Gülbaba and Désirée but not in cultivar Boró, while the number of large tubers was not significantly influenced by nitrogen supply. The tuber weight per plantlet was strongly influenced by genotype. Nitrogen supply of the in vitro plantlets had a prolonged effect on in vitro tuberization. Because the optimum nitrogen treatment is genotype specific, the quantity of large in vitro tubers could be increased by adjusting the nitrogen content of the medium.     

“Head-to-Side-Chain” Cyclodepsipeptides of Marine Origin

Since the late 1980s, a large number of depsipeptides that contain a new topography, referred to as “head-to-side-chain” cyclodepsipeptides, have been isolated and characterized. These peptides present a unique structural arrangement that comprises a macrocyclic region closed through an ester bond between the C-terminus and a β-hydroxyl group, and terminated with a polyketide moiety or a more simple branched aliphatic acid. This structural pattern, the presence of unique and complex residues, and relevant bioactivity are the main features shared by all the members of this new class of depsipeptides, which are reviewed herein.     

Predicting leaf nitrogen content in olive trees using hyperspectral data for precision agriculture

Precision Agriculture - Olive orchard is one of the main crops in the Mediterranean basin and, particularly, in Spain, with 56% of European production. In semi-arid regions, nitrogen (N) is the...     

Differentiation of mycoplasma gallisepticum strains using molecular methods

Increasing use of Mycoplasma gallisepticum (MG) live vaccines has led to a need for the differentiation of MG strains. The MG strains MK-7, MS-16, S6, FS-9 and R strains and the MG live vaccine strain F were compared by random amplification of polymorphic DNA (RAPD) in this study. Using RAPD, different patterns were found among the MG strains. In addition to this, we examined the differentiating potential of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) primers targeted at the crmA, crmB, crmC, gapA, mgc2 and pvpA genes encoding cytadherence-related surface proteins. These proteins may take part in the pathogenesis of MG-induced disease. Differentiation of strain F is based on the identification of restriction enzyme sites in the PCR amplicons. Using HphI enzyme, crmC PCR amplicons produced different RFLP patterns. Digestion of amplicons of gapA-specific PCR with MboI enzyme also produced distinct patterns. Differences were observed among strains R and F by digestion of mgc2 PCR amplicons with HaelIl and VspI enzymes and digestion of pvpA PCR amplicons with AccI, PvulI and ScrFI endonucleases. This method can be used for the rapid differentiation of vaccine strain from wild strains. Differentiation of MG strains is a great advantage for diagnosticians or practitioners and it is useful for epidemiological studies.     

Expression and localisation of claudin-1, -2, -3, -4, -5, -7 and -10 proteins in the normal canine mammary gland

The recently identified claudins are dominant components of tight junctions, responsible for cell adhesion, polarity and paracellular permeability. Certain claudins have been shown to have relevance in tumour development. The aim of the present study was to analyse the expression of claudin-1, -2, -3, -4, -5, -7 and -10 in normal canine mammary glands. Samples from the inguinal mammary regions of 20 non-castrated, 1-13 years old female dogs were studied. Immunohistochemical analysis was performed on conventional specimens and tissue microarrays. The results of the immunohistochemical reactions detecting claudins in tissue sections were photodocumented. The immunoreactivity of claudins was quantitatively analysed on digital images using Leica QWin morphometry software. Intense membranous immunolabelling was found for claudin-1, -3 and -7, intense membranous with non-granular cytoplasmic immunolabelling for claudin-2, moderate membranous immunolabelling for claudin-4 and -5, and weak membranous immunolabelling for claudin-10. The occurrence of tight junctions was confirmed by ultrathin section electron microscopy. The available data suggested that claudins might be proteins preserved throughout the evolution of mammals. The results of our study support the concept that they are indeed preserved, since the same type of claudins, in identical distribution, could be detected in our canine mammary tissue samples as could be found in human mammary tissue.