Autotropism in Fungal Spores

Autotropism was examined in germinating spore pairs of Rhizopusstolonifer, Mucor plumbeus, Trichoderma viride, and Botrytiscinerea. When germinated on agar surfaces the first three speciesexhibited negative autotropism, B. cinerea being neutral inits autotropic behaviour. More pronounced negative autotropismwas shown by the first three species when germinated on a filmof Cellophane applied to an agar surface. Under these conditionsB. cinerea displayed positive autotropism. Spore pairs of R. stolonifer germinated on agar containing cellulosepowder or charcoal showed less negative autotropism than onagar alone. Touching spore pairs of each species showed a markedtendency towards cis-ness, i.e. germ-tubes beginning on thesame side of a line joining the two spore centres, under theculture conditions described, the one exception being the reductionin cis-ness recorded when R. stolonifer was germinated on agarcontaining charcoal. Time courses of germination were determined for single sporesand touching spore pairs of R. stolonifer and M. plumbeus anda significant promotion was obtained in the spore pairs as comparedwith the single spores. Although both these species exhibitmarked negative autotropism there was a strong tendency forthe positive germ-tube, i.e. one beginning more nearly towardsits neighbour, to emerge before the negative germ-tube in thosespore pairs having one germtube positive and the other negativein orientation. Also, in R. stolonifer, the replacement of germination-promotersby germination-inhibitors in filtrates from spore suspensionsas they age is correlated with a change from positive to negativeautotropism in germinating members of (+ –) spore pairs. Possible mechanisms are discussed to account for the observedeffects.     

Carbohydrate Partitioning and Compartmental Analysis for a Highly Productive CAM Plant, Opuntia ficus-indica

Carbon partitioning patterns of Opuntia ficus-indica, a widelycultivated crassulacean acid metabolism species, were analysedto estimate carbon fluxes. After labelling a cladode with ¹⁴CO₂,activities of ¹⁴C in various organs were measured for 6 weeks;the observed ¹⁴C time-courses for ¹⁴C in the labelled cladodeand for transfer into other organs were simulated with a compartmentmodel. Within the first week, half of the newly synthesizedcarbohydrate in the labelled cladode was either converted intostructural material in that cladode, lost by respiration ofthat cladode, or moved to other organs. In the non-labelledcladode and the roots, such newly synthesized carbohydrate initiallyincreased, reached maxima, and then declined. The basal cladodeand the daughter cladode used 65 and 96%, respectively, of theirown assimilate. Roots imported 12 and 2 % of carbohydrate fromthe basal cladode and the daughter cladode, respectively. Whenthe whole plant was shaded, the daughter cladode incorporatednearly threefold more carbohydrate from the basal cladode intostructural material compared with the control. When plants weredroughted, roots incorporated 23 % more and the daughter cladodeincorporated 68 % less carbohydrate from the basal cladode intotheir structural material than for the control. The basal cladodesof the 18-month-old plants exported 60% more carbon than thoseof the 6-month-old plants. Carbon flux rates derived from compartmentalanalysis can be used as parameter values in plant productionmodels. Carbon partitioning, compartment model, drought, plant age, shading     

Chromophore: apoprotein interactions in phytochrome A*

Phytochromes are molecular light switches by virtue of their photochromic red/far-red reversibility. The His-324 residue next to the chromophore-linked Cys-323 plays a critical role in conferring photochromism to the tetrapyrrole chromophore in native phytochrome A. The chromophore appears to be enclosed between the amphiphilic α-helical chains in a hydrophobic pocket. The absorbance maxima of both the Pr and the Pfr forms of pea phytochrome A are blue-shifted by 10 and 20 nm, respectively, upon C-terminal truncation. We speculate that the quaternary structure of the phytochrome A molecule involves some interactions of the C-terminal half with the chromophore domain. The Pfr conformation of phytochrome includes an amphiphilic α-helix of the amino terminal chain, which occurs in 113 ms after picosecond photoisomerization of the Pr form. Compared to α-helical folding, unfolding of the α-helix occurs faster in about 310 μs upon phototransformation of the Pfr form of phytochrome A. The photochromic transformation of phytochrome A modulates protein kinase-catalysed phosphorylation sites in vivo and in vitro, but only a subtle local change in conformation is detectable in the phosphorylated phytochromes. This suggests that the post-translational modification serves as a surface label, rather than a transducer-activating trigger, for the recognition of a putative phytochrome receptor.     

INFLUENCE OF OXIDATION-REDUCTION REDUCTANTS ON SALMONELLA TYPHIMURIUM GROWTH RATES AFTER INITIAL pH ADJUSTMENT AND ZINC COMPOUND ADDITION

The objective of this study was to examine the separate influence of acidic pH, reductants (cysteine and sulfide) and zinc compounds (Zn acetate and Zn sulfate) during anaerobic growth of a S. typhimurium poultry isolate in rich or minimal media. The anaerobic growth of a S. typhimurium poultry isolate in TSB medium was significantly inhibited by either acidic initial pH or higher concentrations of Zn acetate. S. typhimurium anaerobic growth in M9 minimal medium was significantly inhibited by either acidic pH or higher concentrations of Zn acetate or Zn sulfate. Most anaerobic growth rates of the S. typhimurium poultry isolate in acidic media and with higher concentrations of Zn acetate or Zn sulfate were less than 0.10 h^-1. The overall anaerobic growth rates of S. typhimurium were inhibited more in the presence (0.089 h^-1) of reductants than in the absence (0.102 h^-1) of reductants in M9 medium. Results in this study suggest that either increasing Zn concentration or decreasing initial pH can reduce growth rate of foodborne Salmonella under anaerobic growth conditions.     

Molecular Phylogeny among Local Populations of Formica japonica (Hym., Formicidae) in Korea

ABSTRACT Not only were used Random amplified polymorphismic DNA(RAPD) markers as input for an analysis of molecular variance (AMOVA) and cluster analysis to describe the population genetic structure, but also morphometric analysis of Formica japonica in Korea in order to investigate the relationships between local populations according to altitude. The ten populations of F. japonica in Korea did not showed any relationships according to altitude in morphological analysis, while they showed distinct relationship in RAPD analysis. It was noticed that they were clearly separated as four groups according to altitude. The first was Jirisan-Gachilbong- Gyebangsan population, the second Iksansi-Odongdo, the third Deukyusan-Hallasan, the fourth Siheungsi- Seonamsa-Jinjusi. The first group was high mountainous, the second flat and low altitude, the third high mountainous, and the fourth flat and low altitude. They occur from low altitude to comparative high altitude 1,400 m in Korea. Actually, it was found that the relationships of 10 local populations of Korean Formica japonica were not related to morphological evolution, but related to molecular evolutionary data evolved from RAPD analysis.     

APPLICATION OF A TRANSPOSON FOOTPRINTING TECHNIQUE FOR RAPID IDENTIFICATION OF SALMONELLA TYPHIMURIUM TN5 MUTANTS REQUIRED FOR SURVIVAL UNDER DESICCATION STRESS CONDITIONS

Salmonella spp. are one of the foodborne pathogens that can be isolated in the environments of poultry houses and desiccation is a potential stress condition that can influence the survival of Salmonella spp. in this environment. In order to investigate the desiccation survival mechanism of Salmonella spp. the genome of S. typhimurium ATCC 14028 was screened for the genes potentially required for survival during desiccation using a novel method based on Tn5 mutagenesis previously developed in our laboratory. This method, termed transposon footprinting, simultaneously amplifies the Tn5-flanking sequences in a complex pool of the Tn5 mutants. As the length of the amplified DNA fragment should be unique for each distinct Tn5 mutant, the polymerase chain reaction (PCR) products separated on an agarose gel generate transposon footprints with each band in the footprint representing the corresponding Tn5 mutant. By comparing the transposon footprints from the pools of S. typhimurium Tn5 mutants before and after exposure to desiccation, Tn5 mutants that were not recovered after the selection were rapidly identified that would be easily isolated for further genetic analysis.     

General biology of Ostrinia palustralis memnialis (Walker), a potential biological control agent of Rumex spp. in Korea

Ostrinia palustralis memnialis is an oligophagous insect that feeds on the species of the genus Rumex. Continuous rearing of O. palustralis memnialis was carried out from 2004 to 2005, and its general biology was studied. The preliminary host specificity test showed a promising result for O. palustralis memnialis as a potential biological control agent for Rumex spp.