https://yunus.hacettepe.edu.tr/~damlacetin/kmu407/index_dosyalar/4.%20makale.pdf

Biodegradable polymers as biomaterials

I read this book the same weekend that the Packers took on the Rams, and the experience of the latter event, obviously, colored my judgment. Although I abhor anything that smacks of being a handbook (like, \"How to Earn a Merit Badge in Neurosurgery\") because too many volumes in biomedical science already evince a boyscout-like approach, I must confess that parts of this volume are fast, scholarly, and significant, with certain reservations. I like parts of this well-illustrated book because Dr. Sj6strand, without so stating, develops certain subjects on technique in relation to the acquisition of judgment and sophistication. And this is important! So, given that the author (like all of us) is somewhat deficient in some areas, and biased in others, the book is still valuable if the uninitiated reader swallows it in a general fashion, realizing full well that what will be required from the reader is a modulation to fit his vision, propreception, adaptation and response, and the kind of problem he is undertaking. A major deficiency of this book is revealed by comparison of its use of physics and of chemistry to provide understanding and background for the application of high resolution electron microscopy to problems in biology. Since the volume is keyed to high resolution electron microscopy, which is a sophisticated form of structural analysis, but really morphology in a modern guise, the physical and mechanical background of The instrument and its ancillary tools are simply and well presented. The potential use of chemical or cytochemical information as it relates to biological fine structure , however, is quite deficient. I wonder when even sophisticated morphol-ogists will consider fixation a reaction and not a technique; only then will the fundamentals become self-evident and predictable and this sine qua flon will become less mystical. Staining reactions (the most inadequate chapter) ought to be something more than a technique to selectively enhance contrast of morphological elements; it ought to give the structural addresses of some of the chemical residents of cell components. Is it pertinent that auto-radiography gets singled out for more complete coverage than other significant aspects of cytochemistry by a high resolution microscopist, when it has a built-in minimal error of 1,000 A in standard practice? I don't mean to blind-side (in strict football terminology) Dr. Sj6strand's efforts for what is \"routinely used in our laboratory\"; what is done is usually well done. It's just that …

Methods in Enzymology.

Fluorescent and red light environments generate greatly different patterns of pigmentation and morphology in Fremyella diplosiphon. Most strikingly, red-illuminated cultures contain no measurable C-phycoerythrin and have a mean filament length about 10 times shorter than fluorescent-illuminated cultures. C-phycoerythrin behaves as a photoinducible constituent of this alga. Spectrophotometric and immunochemical procedures were devised so that C-phycoerythrin metabolism could be studied quantitatively with [(14)C]-phenylalanine pulse-chased cultures. Transfer of red-illuminated cultures to fluorescent light initiates C-phycoerythrin production by essentially de novo synthesis. C-phycoerythrin is not degraded to any significant extent in cultures continuously illuminated with fluorescent light. Transfer of fluorescent-illuminated cultures to red light causes an abrupt cessation of C-phycoerythrin synthesis. The C-phycoerythrin content of cultures adapting to red light decreases and subsequently becomes constant. Loss of C-phycoerythrin is not brought about by metabolic degradation, but rather by a decrease in mean filament length which is effected by transcellular breakage. In this experimental system, light influences intracellular C-phycoerythrin levels by regulating the rate of synthesis of the chromoprotein.

/pdf/complementary-chromatic-adaptation-in-a-filamentous-blue-28x8iapqkx.pdf

Complementary chromatic adaptation in a filamentous blue-green alga

Oxygen relations of nitrogen fixation in cyanobacteria.

Heterocysts are differentiated cells that are specialized for fixation of N2 in an aerobic environment. In heterocysts in the light, Photosystem I generates ATP, but no photosynthetic production of O2 takes place. Instead, reductant moves into heterocysts from vegetative cells. In return, fixed nitrogen moves from heterocysts to vegetative cells. In neither case is there certainty about the identity of the traffic molecules. Pathways of electron-donation to N2 have been extensively investigated, but their in-vivo importance remains to be critically tested. Nitrogenase in heterocysts is protected from inactivation by O2 by a variety of means, principally by enhanced respiration and by a barrier, the heterocyst envelope, to entry of O2. However, the respiratory apparatus and the biosynthetic processes that result in synthesis of the barrier have been little studied. The detailed mechanisms underlying metabolic, environmental, and developmental control of nitrogenase are under investigation. Studies of heterocyst development are being greatly facilitated by recent advances in the genetics of Anabaena sp. An autoregulated gene, hetR, that is activated shortly after nitrogen-stepdown is critical for the differentiation of heterocysts. Two enigmas remain to be answered: how is it determined which cells will differentiate; and, after differentiation is initiated, what intercellular interactions and intracellular mechanisms regulate the progression of the differentiation process? An evolutionary and biochemical relationship between the processes leading to the formation of heterocysts and akinetes is suggested.

Heterocyst Metabolism and Development

The cyanophycin granules from two-week-old cultures of the blue-green alga Anabaena cylindrica were isolated by sonication of the cells followed by differential centrifugation. These particles are composed of polypeptides containing only two amino acids, aspartic acid and arginine, and have a molecular weight between about 25,000 and 100,000.

https://www.pnas.org/content/pnas/68/2/265.full.pdf

Cyanophycin Granules from the Blue-Green Alga Anabaena cylindrica: A Reserve Material Consisting of Copolymers of Aspartic Acid and Arginine

Determination of the structure of the novel polypeptide containing aspartic acid and arginine which is found in cyanobacteria

An assay was developed to determine the amount of cyanophycin granules in blue-green algae. The amount of this polypeptide in cells of Anabaena cylindrica was measured as a function of culture age and was compared with changes in other proteinaceous cellular components. The data presented support the notion that the cyanophycin granule is a cellular nitrogen reserve.

Measurement of the Cyanophycin Granule Polypeptide Contained in the Blue-Green Alga Anabaena cylindrica

Granules isolated from the blue-green alga Anabaena cylindrica and composed of copolymers of arginine and aspartic acid have the electron microscopic aspects of structured granules and the solubility and certain of the staining properties of cyanophycin granules. Material which accumulates at the poles of heterocysts may have a similar composition.

Correspondence of cyanophycin granules with structured granules in Anabaena cylindrica

Heterocysts of autotrophically grown Anabaena cylindrica contain about 77% as much chlorophyll as do vegetative cells, have little phycocyanin, and appear to lack myxoxanthophyll. Heterocysts have a photosystem I. Lipids of the two cell types differ.

Robert D. Simon

Papers

Cyanophycin Granules from the Blue-Green Alga Anabaena cylindrica: A Reserve Material Consisting of Copolymers of Aspartic Acid and Arginine

Determination of the structure of the novel polypeptide containing aspartic acid and arginine which is found in cyanobacteria

Measurement of the Cyanophycin Granule Polypeptide Contained in the Blue-Green Alga Anabaena cylindrica

Correspondence of cyanophycin granules with structured granules in Anabaena cylindrica

Pigments and lipids of heterocysts