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H Reichenbach

Publications and source records attributed to H Reichenbach.

89 records · Page 5Linked to original sources

The fine structure of Herpetosiphon, and a note on the taxonomy of the genus.

The fine structure of the Gram-negative filamentous gliding bacterium, Herpetosiphon is described. The outer membrane of the cell envelope could not be resolved as a separate structure, probably because it is fused with the underlying dense (peptidoglycan) layer. There was an additional wall layer outside this membrane-peptidoglycan complex, but a sheath in the classical sense, as postulated in the definition of the genus, was lacking. On the cell surface a loose network of fibrils could be seen. Inside the cells 3 types of intracytoplasmic membranes were discernible: a) true mesosomes near cross walls; b) a system of coarser membranes which was not connected with the septa and formed networks or tubular complexes; c) degenerated septa within bulbs. The bulbs are swollen sections of filaments, occurred mainly in ageing cultures, and are probably a degeneration phenomenon. The filaments contained necridia, i.e. dead and empty cells, across which breaks may occur so that empty cell wall cylinders remain attached to the ends of the daughter filaments, falsely suggesting the presence of a sheath. The taxonomy of Herpetosiphon is discussed in detail: The organism has been described before as Flexibacter giganteus. It is proposed to abandon the species H. aurantiacus in favor of H. giganteus, but to retain the genus Herpetosiphon. An improved definition of the genus is given.

Cell Wall↗

Structural changes in Stigmatella aurantiaca during myxospore induction.

Suspension cultures of Stigmatella aurantiaca (Chondromyces aurantiacus) were induced to form myxospores by addition of glycerol to the growing culture. The cells were fixed at various stages during conversion, thin sections were prepared, and changes in fine structure were studied. Vegetative cells are quite similar in their ultrastructure to Myxococcus xanthus. During transformation into myxospores, three important cytological changes were observed. Granules of storage material, probably polysaccharide and polyphosphate, accumulated; a 200 to 300-mum thick capsule was laid down, and the outer triple layer of the cell wall became locally folded. These cell wall folds were often densely packed and lay in pockets formed by the cytoplasmic membrane. We have suggested the possibility that the cell may store in these folds wall material which has become superfluous by the decrease in surface area during conversion.

Bacteria↗

Fine structure of fruiting bodies of Stigmatella aurantiaca (Myxobacterales).

The fruiting body of Stigmatella aurantiaca consists of a thick stalk supporting a number of individual cysts. The stalk is made of discontinuous tubules, of dimensions known for vegetative cells, which are oriented parallel to the longitudinal axis of the stalk. The red-brown cysts contain numerous, randomly oriented myxospores which are surrounded by thick, fibrous capsules. Their cell walls are wavy or ruffled and exhibit fewer budlike infoldings than reported for myxospores induced in liquid. We suggest that the extended time period available for metabolic and regulatory adjustments by the cell during morphogenesis within cysts accounts for the presence of considerably fewer deep cell wall infoldings than in glycerol-induced myxospores.

Bacteria↗

[Roberts syndrome with aneurysm of the interatrial septum, cow milk protein intolerance and absent swallowing reflex].

A three years old girl with Roberts-syndrome is presented in this report. An aneurysm of the interatrial septum without hemodynamic significance was found besides the typical symptoms of the Roberts-syndrome. The child had to be fed by nasogastral tube for more than two years because of never feeling hungry and lacking reflex to swallow. A pulmonary and intestinal reaction during the provocation with cowmilkprotein-containing food was observed additionally, so that we had to give an cowmilkprotein-free diet until the age of 28 months. The majority of reported cases with Roberts-syndrome showed characteristic cytogenetic abnormalities. The karyotype of our patient was normal. Roberts syndrome is an autosomal recessive disorder. We recommended repeated ultrasound examinations during the next pregnancy because of the 25% recurrence risk on subsequent siblings. The prognosis quoad vitam in patients with Roberts-syndrome remains poor. However, the development in our patient stresses the eminent value of medical and social support for those seriously handicapped children.

Abnormalities, Multiple↗