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ADENOSINE 5'-TRIPHOSPHATE-ARGININE PHOSPHOTRANSFERASE FROM LOBSTER MUSCLE: PURIFICATION AND PROPERTIES.

1. A simple chromatographic method is described for the purification of arginine kinase from lobster (Homarus vulgaris) muscle. 2. Some physical properties and the effects on enzyme activity of ionic strength, pH, buffer salts, metal ions and substrates are reported. 3. The kinetic parameters, evaluated by variation of the concentration of one of the substrates, are dependent on the concentration of the other substrate. 4. The properties of the enzyme are discussed in relation to previous findings about phosphagen phosphotransferases.

Adenosine↗

Two proteins purified from lobster nerve extract; isolation and physicochemical characterization.

1. A protein component, fraction B, of lobster nerve extracts has been isolated and purified by differential ultracentrifugation and precipitation with zinc acetate. 2. Physicochemical data obtained from this protein and from fraction C are summarized. 3. Fraction B is present in lobster nerve extracts in higher concentration (relative to fraction A) than in blood. 4. A second component, fraction C, of sedimentation constant S(20) (o) = 13.2 has been isolated from lobster nerve extracts.

Animals↗

ELECTRON MICROSCOPE STUDIES ON DEVELOPING CRAYFISH OOCYTES WITH SPECIAL REFERENCE TO THE ORIGIN OF YOLK.

The endoplasmic reticulum is composed, in places, of stacks of parallel cisternae which are limited by membranes having great numbers of ribosomes attached to their outer surface. These are connected with other cisternae of similar structure but with fewer ribosomes and without preferred orientation. The latter extend in all directions from the stacked cisternae, branching and anastomosing freely so that the entire system of membrane-limited cisternae appears interconnected; a morphological condition suitable to serve as the basis for an active transport system. Within the stacked cisternae appear granules about 40 to 60 mmicro in diameter. These are thought to represent the precursors of proteinaceous yolk, and the hypothesis is advanced that most of the intracisternal granules are synthesized here, possibly under the influence of the ribosomes. They then "flow" into and along the unoriented cisternae to regions where they collect, expand the cisternae, and undergo transformation into finely granular, relatively large proteinaceous yolk bodies. The mitochondria are somewhat pleomorphic, often show atypical cristae, and frequently contain a few dense granules. Lipid is abundant. Other cytoplasmic components are illustrated.

Animals↗

OBSERVATIONS ON THE VARIATIONS IN SIZE OF THE A REGION OF ARTHROPOD MUSCLE.

The muscles of three different arthropods, a mite, a fly, and an ostracod, show variations in the length of the A region within a given individual. There is no indication that the observed differences in A band length are related to the functional state of the muscle since little, if any, decrease in the length of the A bands was noted when sarcomeres shortened. The length of the A region was determined by polarized light microscopy and in the case of the mite and the ostracod this measurement was made on intact muscles. It is concluded that the size of the A filaments in an individual can vary in a manner unrelated to immediate functional changes. The I filaments may vary in size, but this could not be clearly demonstrated.

Animals↗

Morphology of the ommatidia of the compound eye of Limulus.

The sensory portion of the ommatidium of the compound eye of Limulus has been studied with the electron microscope. In axial longitudinal section the rhabdom appears to be made up of small polygons, and in transverse section the rhabdom appears as a banded structure of dark lines. Thus in three dimensions the rhabdom resembles a honeycomb composed of tubular units, the long axes of which lie in transverse planes and are oriented perpendicular to the retinula cell's contours. The tubular units, which are about 140 mmicro in diameter in Limulus (70 mmicro in diameter in the spider and Scutigera), are microvilli of the borders of the retinula cells. The walls of these microvilli are continuous with fine linear structures (membranes) in the cytoplasm of the retinula cells. In transverse sections of the ommatidium oval bodies interpreted as mitochondria are observed in an annular zone at the tips of the rhabdom's rays. These mitochondria, which are 2 to 10 micro in diameter, are crowded with irregular closed outlines about 100 mmicro in diameter. Possible functions of components of the ommatidium are discussed.

Animals↗

Basophilic lamellar systems in the crayfish spermatocyte.

Histochemical procedures for the demonstration of RNA have shown the presence of intensely basophilic bodies in the cytoplasm of spermatocytes of the crayfish, Cambarus virilis. The staining of thick sections, cut alternately with thin sections for electron microscopy, has permitted identification of the basophilic bodies with two types of lamellar systems. One of these, a set of straight annulate lamellae, is restricted to meiotic prophase. The second type of lamellar systems has been found from late prophase to early spermatid stages. It consists of an ellipsoidal lamellar set which intersects a number of straight lamellae. Within the region of intersection, the ellipsoidal lamellae break up into an array of small tubules of about 150 A diameter. The term tubulate lamellar system was chosen to designate this type of lamellar complex. Small RNA-containing granules could not be detected in annulate lamellar systems. While there are a few granules in the marginal regions of the tubulate lamellar system, their distribution cannot be responsible for the basophilia which is intense within all regions of the lamellar body.

Animals↗

Some observations on the fine structure of the sinus gland of a land crab, Gecarcinus lateralis.

The dilated axon endings of the sinus glands of the brachyuran crab, Gecarcinus lateralis, are filled with homogeneously dense granules, each granule being bounded by a delicate membrane. The granules are of two orders of magnitude: 0.05 to 0.1 micro and 0.15 to 0.2 micro in diameter. Each axon ending contains granules of a nearly uniform size. Endings with granules of the larger size range predominate. Non-nervous cells endogenous to the sinus gland are scattered among the nerve endings. The cell contours are irregular, and cytoplasmic processes ramify between endings. The axons are unmyelinated, having only thin limiting membranes, and they possess many neurofibrils. Granules in preterminal portions of the axons tend to lie at the periphery of the fiber, and in some cases in chains at the core of the fiber. The granules appear to be storage and release centers for neurosecretory substances or their precursors.

Animals↗

The formation of intracellular crystals in midgut glands of Limnoria lignorum.

Certain morphological features of intracellular crystal formation within the midgut glands of Limnoria lignorum (Rathke) have been studied with the electron microscope and cytochemical methods. A correlation has been established between Golgi membranes and formation of the crystals. The Prussian blue reaction reveals quantities of iron localized in the intracellular crystals and in small granular structures seen in the apical region of the cells. These granules can be identified as accumulations of Golgi membranes, with which iron-containing particles are associated. When these membrane configurations are studied with the electron microscope, they can be classified and arranged in an assumed sequence which is thought to represent successive stages in the development of crystals. As the membrane systems become progressively specialized, increasing accumulations of dense granular material appear within their interstices. This material is rich in iron and probably represents the component responsible for the positive Prussian blue reaction. This material also appears to be a precursor substance for iron-containing protein molecules which are synthesized and arranged to make up the crystals. These iron-containing molecules are first deposited in orderly array as double rows of dense particles on certain internal membranes of the specialized Golgi complexes. The membranes later disappear and the particles form definitive crystals by rearrangement into a hexagonal close-packed pattern.

Animals↗