A mitogen-activated protein kinase kinase required for induction of cytokinesis and appressorium formation by host signals in the conidia of Colletotrichum gloeosporioides.
(9/329)
Differentiation of fungal conidia of phytopathogens into the infection structure, appressorium, requires contact with a hard surface and host signals. The molecular signaling involved in the induction of this differentiation is poorly understood. We report the cloning of a mitogen-activated protein kinase kinase (MEK), CgMEK, from Colletotrichum gloeosporioides and its role in the induction of these developmental processes involved in pathogenesis. Disruption of CgMEK1 resulted in the loss of its ability to form appressoria in response to the host's signals and a loss of virulence. Results of confocal microscopic examination of germinating conidia of the gene-disrupted mutants were similar to those for wild-type conidia treated with an MEK inhibitor, suggesting that CgMEK1 is involved in two developmental processes in the differentiation into appressorium: (1) polarized cell division, with the preferential increase in F-actin in one of the daughter nuclei after nuclear division and the formation of septum; and (2) differentiation of the germ tube into an appressorium. CgMEK1 is required for the differentiation. (+info)
Incorporation of lipid into the epicuticle of Rhodnius (Hemiptera).
(10/329)
The incorporation of lipid into both the outer and inner epicuticle during deposition is described. Waterproofing of the epicuticle by secretion of the wax layer, and sclerotization with or without melanization, are controlled from a distance by the epidermal cells by way of the pore canals. The pore canals gradually narrow as they approach the epicuticle. On reaching the inner epicuticle the canal ends in a conical projection from the apex of which a permeable lipophilic channel about 20-25 nm in diameter runs vertically to the apex of which a permeable lipophilic channel about 20-25 nm in diameter runs vertically to the surface. Shortly before ecdysis, silver-binding material (perhaps protein rich in tyrosine, or other precursors concerned in sclerotization) spreads radially from a point in the cuticular channels just below the outer epicuticle, and gradually impregnates the outer two thirds or more of the inner epicuticle. The precise pattern varies in different cuticular structures. Argentaffin materials (polyphenols) first appear in these same sites at the time of ecdysis and increase rapidly during the next 24 h. Lipid appears in the lumen of the distal parts of the pore canals (with a patchy distribution) shortly before ecdysis. When digestion and absorption of the old endocuticle are almost complete, minute lipid droplets appear on the surface of the epicuticle, apparently exuded from the epicuticular channels, and spread to make a uniform layer. When first formed this layer strains readily with Sudan B, but the lipid becomes incorporated in a delicate non-lipid silver-binding membrane (also exuded from the epicuticular channels) and hardens just before ecdysis, to form the so-called 'wax layer' which then no longer stains with Sudan B. Within half an hour after ecdysis the alcian blue-staining cement layer is poured out by the dermal glands, and forms a continuous but somewhat irregular covering over the 'wax layer'. Changes in the epicticle that accompany the repair of abrasions are described. (+info)
Comparative analysis of the lipids of Acinetobacter species grown on hexadecane.
(11/329)
A comparative analysis of the cellular and extracellular lipids of Acinetobacter species HO1-N indicated basic physiological differences in hexadecane-grown cells. The cellular lipids obtained from hexadecane-grown cells were characterized by 3- and 18-fold increases in the phospholipid fraction and the mono- and diglyceride fraction, respectively, over that obtained from nutrient broth-yeast extract-grown cells. The cellular-associated pools of hexadecane were shown to comprise approximately 8% of the dry cell weight of hexadecane-grown cells. The extracellular lipids obtained from the culture broths of hexadecane-grown cells were comprised of triglyceride, mono- and diglyceride, free fatty acid, and wax ester. These lipids were either absent or present in minor concentrations in the culture broths of nutrient broth-yeast extract-grown cells. The exponential growth of Acinetobacter sp. on hexadecane was characterized by the significant accumulation of free fatty acid, monoglyceride, and diglyceride in the culture medium. Wax ester was shown to represent a minor portion of the extracellular lipids during the exponential growth phase, appearing in significant proportion only after the culture had entered the stationary phase of growth. (+info)
Strains of Pseudomonas putrefaciens from clinical material.
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Eight strains of Pseudomonas putrefaciens have been received from among 466 strains of Pseudomonas submitted to the Computer Trials Laboratory for identification over the last eight years. Two of the strains of P. putrefaciens from patients with otitis media and otitis externa respectively appear to have played a pathogenic role. The biochemical characteristics of these eight strains were compared with those of seven culture collection strains. (+info)
Specific heat determination of plant barrier lipophilic components: biological implications.
(13/329)
The specific heat of isolated plant cuticles and their corresponding cuticular waxes have been measured for the physiological temperature in the range of 273-318 K at regular intervals. C(p) values ranged from 1.5 up to 4 J K(-1) g(-1) indicating a high cohesion, at the molecular level, of the molecular lipophilic components that constitute the plant cuticle. Second order phase transitions around 293 K, assigned to the cuticular matrix mainly constituted of the biopolyester cutin, have been detected and measured. Ecophysiological and physical implications of these thermodynamic data are discussed. (+info)
Chemical composition of the Prunus laurocerasus leaf surface. Dynamic changes of the epicuticular wax film during leaf development.
(14/329)
The seasonal development of adaxial Prunus laurocerasus leaf surfaces was studied using newly developed methods for the mechanical removal of epicuticular waxes. During epidermal cell expansion, more than 50 microg leaf(-1) of alkyl acetates accumulated within 10 d, forming an epicuticular wax film approximately 30 nm thick. Then, alcohols dominated for 18 d of leaf development, before alkanes accumulated in an epicuticular wax film with steadily increasing thickness (approximately 60 nm after 60 d), accompanied by small amounts of fatty acids, aldehydes, and alkyl esters. In contrast, the intracuticular waxes stayed fairly constant during development, being dominated by triterpenoids that could not be detected in the epicuticular waxes. The accumulation rates of all cuticular components are indicative for spontaneous segregation of intra- and epicuticular fractions during diffusional transport within the cuticle. This is the first report quantifying the loss of individual compound classes (acetates and alcohols) from the epicuticular wax mixture. Experiments with isolated epicuticular films showed that neither chemical conversion within the epicuticular film nor erosion/evaporation of wax constituents could account for this effect. Instead, transport of epicuticular compounds back into the tissue seems likely. Possible ecological and physiological functions of the coordinate changes in the composition of the plant surface layers are discussed. (+info)
Protecting against water loss: analysis of the barrier properties of plant cuticles.
(15/329)
The cuticle is the major barrier against uncontrolled water loss from leaves, fruits and other primary parts of higher plants. More than 100 mean values for water permeabilities determined with isolated leaf and fruit cuticles from 61 plant species are compiled and discussed in relation to plant organ, natural habitat and morphology. The maximum barrier properties of plant cuticles exceed that of synthetic polymeric films of equal thickness. Cuticular water permeability is not correlated to the thickness of the cuticle or to wax coverage. Relationships between cuticular permeability, wax composition and physical properties of the cuticle are evaluated. Cuticular permeability to water increases on the average by a factor of 2 when leaf surface temperature is raised from 15 degrees C to 35 degrees C. Organic compounds of anthropogenic and biogenic origin may enhance cuticular permeability. The pathway taken by water across the cuticular transport barrier is reviewed. The conclusion from this discussion is that the bulk of water diffuses as single molecules across a lipophilic barrier while a minor fraction travels along polar pores. Open questions concerning the mechanistic understanding of the plant cuticular transport barrier and the role the plant cuticle plays in ensuring the survival and reproductive success of an individual plant are indicated. (+info)
TLC, GLC and MS of complex lipid mixtures from uropygial secretions.
(16/329)
A general technique of investigation of uropygial gland secretions is described including sample collection and extraction as well as partition, TLC and column chromatography of the crude lipids. The main components, generally ester waxes, are cleaved by CH3OH/HCl followed by conversion into fractions ready for GLC. Some GLC and MS details are reported. (+info)