Effect of fruit load on 9,10-ketol-octadecadienoic acid (KODA), GA and jasmonic acid concentrations in apple buds

The relationship between 9,10-ketol-octadecadienoic acid (KODA), GAs and jasmonic acid (JA) and flower bud formation influenced by fruit load in apples (Malus domestica Borkh.) was investigated. The endogenous KODA and JA concentrations in apical buds in plants subjected to flower thinning treatment (FTT), under which all flowers were removed were higher than those in plants subjected to heavy crop treatment (HCT), under which the number of leaves per fruit was adjusted to 20 from 60 to 120 days after full bloom (DAFB). In contrast, the gibberellic acid concentrations [total of gibberellin A₁ (GA₁) and gibberellin A₄ (GA₄)] in FTT plants were low compared with those in HCT plants. The result suggests that KODA and JA in contrast to GAs may have opposite effects on flower bud formation which is significantly influenced by fruit load in apples and that KODA and JA may also be associated with flower bud formation in apples.     

Composites of wood and trans-1,4-isoprene rubber II: Processing conditions for production of the composites

 The occurrence of grafting between WF and MTIR through esterification, the processing conditions for production of the composites, and the effect of MAH concentration on some physical and mechanical properties as well as the biodegradability of the composites have been studied. The FTIR measurement demonstrated that grafting through esterification had been attained between OH-groups of WF and acid anhydride groups of MTIR during kneading. The optimum kneading conditions for preparing the composites were 120 °C, 30 ∼ 90 rpm for 10 min. The tensile properties of the composites with WF based filler are greater than those with CS (corn starch) based filler. Addition of 10% of MTIR•10 and 8% MAH prepared using the two-step and one-step process, respectively to the TIR-WF composites gave the best result of tensile properties. The presence of MAH in the TIR-WF composites also improved the dimensional stabilization of the resulting composites. The tensile strengh of the composites prepared using the one-step process was about 90% of the composite prepared using the two-step process. The composites of TIR-WF with MTIR compatibilizer had slightly less resistance against subterranean termite (C. formasanus), brown-rot fungus (T. palustris), and white-rot fungus (C. versicolor) and slightly more resistance against bacteria (Bacillus sp.), within the experimental conditioned adopted. Received 8 February 1999     

Preparation and characterization of the phenolated wood using hydrochloric acid (HCl) as a catalyst

Summary Birch (Betula maximowicziana Regel) wood meal was liquefied in the presence of phenol using hydrochloric acid (HCl) as a catalyst at a temperature of 150 °C for 2 h in an autoclave. It was found out that HCl acid could be used as an effective catalyst for the hydroxy phenylation of wood under the experimental conditions. In this study the effect of the concentration of the acid catalyst and the phenol-to-wood ratio on the liquefaction were investigated. The results showed that the phenol-to-wood ratio and the concentration should be increased to a certain degree in order to achieve a less residual rate and sufficient amount of combined phenol. The phenolated woods had apparent flow temperatures in the range of 134.4 to 199.8 °C, being higher than that of a commercial novolak resin. Furthermore, increases in the HCl concentration during liquefaction reaction led to increase in the apparent flow temperature of the resulting phenolated woods. However, the changes in the liquid ratio did not bring about evident changes. The relationship between shear stress (τ) and shear rate showed that the phenolated wood resin melts were shear thinning fluids. The dependences of the apparent melt-viscosities (η) of the phenolated woods and a commercial novolak resin on the shear rates ( ) have the similar tendencies, however, it was found the viscosities of the phenolated woods are about one order higher than that of commercial novolak resin.     

Screening of heterozygous DNA markers in shiitake (Lentinula edodes) using de-dikaryotization via preparation of protoplasts and isolation of four meiotic monokaryons from one basidium

A suitable screening method for heterozygous DNA markers in shiitake,Lentinula edodes (Berk.) Pegler, is reported. Monokaryons were derived from a dikaryon by de-dikaryotization via protoplast formation. Compatibility of the monokaryons was determined by pairwise culture on agar plates. We selected the primers to amplify polymorphic fragments among the original strain (Hokken600H600) and two monokaryons (H600PP-39 and H600PP-67) showing compatibility. A total of 135 fragments were selected as specific random amplified polymorphic DNAs (RAPDs) resulting from 56 primers of the 147 primers tested. Furthermore, we tested whether the polymorphic fragments segregated into 22 among four strains isolated from a basidium. Most of the polymorphic fragments (about 97.8%) showed 22 segregation among the four strains. We concluded that the polymorphic fragments were heterozygous if they were detected in either of the monokaryons (H600PP-39 and H600PP-67) and segregated to 22 among four meiotic strains (H600B-1,-2, -3, and -4). A total of 132 heterozygous DNA markers were therefore selected from a dikaryon of shiitake (Hokken600H600).Part of this report was presented at the 8th Annual Meeting of Mushroom Science and Biotechnology and the 47th Annual Meeting of the Japan Wood Research Society, Kochi, 1997     

Systemic candidiasis in a dog, developing spondylitis

A 4-year-old male Shiba dog initially presented with pain of an undetermined origin and hypersensitivity to touch. Seven days later, the dog developed ataxia, hind-leg weakness and knuckling. The dog died on 20 days after presentation. Postmortem examination revealed a mass in the body of thoracic vertebra. Histopathologically, the mass consisted of granulomatous inflammation, including fungal organisms that were immunohistochemically positive for Candida albicans. Similar granulomatous lesions were observed in the systemic lymph nodes, kidneys, pancreas, spleen, prostate gland, thyroid glands and heart. This case was diagnosed as systemic candidiasis with spondylitis.     

A binding protein for fungal signal molecules in the cell wall of Pisum sativum

In the plant cell wall of Pisum sativum seedlings, we found an NTPase (E.C. 3.6.1.5.) with ATP-hydrolyzing activity that was regulated by an elicitor and suppressors of defense from pea pathogen Mycosphaerella pinodes. The ATPase-rich fraction was purified from pea cell walls by NaCl solubilization, ammonium sulfate precipitation, and chromatography with an ATP-conjugated agarose column and an anion-exchange column. The specific activity of the final ATPase-rich fraction increased 600-fold over that of the initial NaCl-solubilized fraction. The purified ATPase-rich fraction also had peroxidase activity and generated superoxide, both of which were regulated by the M. pinodes elicitor and suppressor (supprescins). Active staining and Western blot analysis also showed that the ATPase was copurified along with peroxidases. In this fraction, a biotinylated elicitor and the supprescins were bound primarily and specifically to ca. 55-kDa protein (CWP-55) with an N-terminal amino acid sequence of QEEISSYAVVFDA. The cDNA clone of CWP-55 contained five ACR domains, which are conserved in the apyrases (NTPases), and the protein is identical to a pea NTPase cDNA (GenBank accession AB071369). Based on these results, we discuss a role for the plant cell wall in recognizing exogenous signal molecules.     

The respiratory burst activity of bottlenose dolphin neutrophils elicited by several stimulants

To investigate the early host defense function in aquatic animals, the respiratory burst activity of bottlenose dolphin neutrophils against soluble and particulate stimulants was measured by luminol-dependent chemiluminescence assays and compared with those of bovine and human. Dolphin neutrophils generated the respiratory burst in response to phorbol 12-myristate 13-acetate (PMA), concanavalinA (ConA), heated-plasma (HP), and homologous-plasma opsonized zymosan except N-formyl-Met-Leu-Phe (fMLP). However, the respiratory burst of dolphin neutrophils stimulated by lipopolysaccharide and Staphylococcus aureus was inferior to those of bovine and human. Furthermore, DP-OZ also induced the respiratory burst of bovine and human neutrophils. In conclusion, dolphin neutrophils responded to several soluble and particulate stimulants as well as human neutrophils, but were refractory or slightly responded to bacterial agents.     

Identification of genes expressed during spore germination of Mycosphaerella pinodes

Mycosphaerella blight, caused by Mycosphaerella pinodes, is one of the major diseases of cultivated pea (Pisum sativum L.). To isolate the genes that are up- and down-regulated during spore germination, suppression subtraction hybridization (SSH) was performed between ungerminated and germinated spores. The 232 and 128 clones from forward and reverse libraries, respectively, were collected, sequenced, and analyzed with a BLASTX homology search. About 95% of the 32 selected clones were expressed during spore germination on a paper sheet and during infection of pea leaves. We discuss the applicability of the SSH libraries for analyzing M. pinodes genes involved in the early stage of infection.