Elucidation of the nature and function of the granular oyster amebocytes through histochemical studies of normal and traumatized oyster tissues

Summary A remarkable humoral component of the oyster inflammatory response was elucidated by employing the tools of the determinative histochemist. The humoral component, characterized by the release of copper and a diazotized p-nitroaniline-positive material from an acidophilic granular amebocyte, was associated with the oyster inflammatory reaction. Grossly, this humoral response was associated with the appearance of an avocado or pea green coloration in the traumatized area. A second amebocytic cell type, termed the basophilic granular amebocyte, was observed swelling in traumatized areas and may have released an additional humoral component into injured regions. Copper released in response to trauma was bound to the cells in and around the wound site and appeared to be most avidly bound by the granules of the basophilic granular amebocytes. Once incorporated into the granular matrix of these amebocytes, copper appeared to stabilize and prevent the granule from swelling.A portion of this work was excerpted from a Ph.D. thesis submitted to the Graduate School, University of Washington, Seattle.This work was supported by Public Health Service Contract No. 5 to 1 ES 00038-02. The costs of publication were defrayed in part by HSAA Award No. RR 06138 and Tumor Biology Training Grant, NIH CA 05245.     

Adenine nucleotide binding sites in normal and mutant adenosine triphosphatases of Escherichia coli

Three types of assays were used to characterize adenine nucleotide binding sites on the Ca²⁺, Mg²⁺-activated ATPase of normal Escherichia coli and its unc A 401 and unc D 412 mutants. ADP was bound mainly at a single site in normal and mutant ATPase. In the absence of divalent cations ATP was bound at a single high-affinity and three low-affinity sites in normal and unc D ATPases. The 2′,3′-dialdehyde (oADP) obtained by periodate oxidation of ADP reacted with both low- and high-affinity sites whereas oATP was bound primarily at a low-affinity site. Two types of adenine nucleotide binding sites, a high-affinity site reacting with ATP and ADP and a low-affinity site for ATP, were detected by the effects of these nucleotides on the fluorescence of the aurovertin D-ATPase complex. This high-affinity site(s) was present in normal and mutant ATPases. However, the fluorescence response at both high- and low-affinity sites was modified in the unc D ATPase as a consequence of the abnormal β subunit in this enzyme. Normal fluorescence responses were not induced by the binding of oADP or oATP to the ATPases. ATP was bound at a single site on isolated α subunits of the enzyme. Since this site was not detected in the unc A ATPase, it is unlikely to be the high-affinity site detected in the intact enzyme or the binding site for the endogenous tightly bound adenine nucleotides found in the purified ATPase. It is more probable that the site detected on the isolated α subunit from the normal enzyme is that which binds oADP since this site was absent in the unc A ATPase. Pretreatment of the normal ATPase with either N, N′-dicyclohexyl-carbodiimide (DCCD) or with 4-chloro-7-nitrobenzofurazan (NbfCl), reagents which inhibit ATPase activity by reacting with a β subunit, affected binding of oADP to α subunit(s) but had less effect with oATP. Inhibition of oADP binding could be due to conformational changes induced in the α subunit by the reaction of DCCD and NbfCl with a β subunit, or to steric reasons. If the latter hypothesis is correct, the active site of the ATPase would be at the interface between α and β subunits of the enzyme.     

Antigenic relatedness of Proteus mirabilis and Escherichia coli with rat tissues and human erythrocytes

The cross-reactions of rat kidney with P. mirabilis and E. coli, and of rat urinary bladder with P. mirabilis were established by precipitation, agglutination and immunofluorescence methods. One of the cross-reactive bacterial components was the lipopolysaccharide. Human erythrocytes of Blood-groups A, O and AB were agglutinated by antisera to P. mirabilis and E. coli. The role of antigenic relatedness in urinary tract infections is discussed.     

Expression of the cloned ColE1 kil gene in normal and Kilr Escherichia coli

The kil gene of the ColE1 plasmid was cloned under control of the lac promoter. Its expression under this promoter gave rise to the same pattern of bacterial cell damage and lethality as that which accompanies induction of the kil gene in the colicin operon by mitomycin C. This confirms that cell damage after induction is solely due to expression of kil and is independent of the cea or imm gene products. Escherichia coli derivatives resistant to the lethal effects of kil gene expression under either the normal or the lac promoter were isolated and found to fall into several classes, some of which were altered in sensitivity to agents that affect the bacterial envelope.     

Adhesion partitioning: intrasomatic observations on normal Escherichia coli and T2 bacteriophage

Adhesion partitioning is a method for progressively dismantling small biological entities for observation of their internal structures. The method is particularly well suited to use with the electron microscope. Objects to be partitioned are air-dried between two preformed plastic films resulting in envelopment of the objects. On separating the films the objects are partitioned. Partitioned E. coli bacteria reveal a variety of structures which change markedly with culture age. Organisms from young cultures have a water-retaining gelatinous matrix in which radially striated discs, fabric-like structures, and microsomes are found. Older cultures are less anatomically complex. The T2 bacteriophage is shown to be composed of an outer limiting membrane and a cohesive semisolid fibrillar body substance, presumably nucleic acid, which can be drawn as a strand from the bacteriophage body.     

The pseudouridine synthase RluD is required for normal ribosome assembly and function in Escherichia coli

RluD is the pseudouridine synthase responsible for the formation of Psi1911, Psi1915, and Psi1917 in Escherichia coli 23S rRNA. Previous work from our laboratory demonstrated that disruption of the rluD gene and/or loss of the pseudouridine residues for which it is responsible resulted in a severe growth phenotype. In the current work we have examined further the effect of the loss of the RluD protein and its product pseudouridine residues in a deletion strain lacking the rluD gene. This strain exhibits defects in ribosome assembly, biogenesis, and function. Specifically, there is a deficit of 70S ribosomes, an increase in 50S and 30S subunits, and the appearance of new 62S and 39S particles. Analysis of the 39S particles indicates that they are immature precursors of the 50S subunits, whereas the 62S particles are derived from the breakdown of unstable 70S ribosomes. In addition, purified mutant 70S ribosomes were found to be somewhat less efficient than wild type in protein synthesis. The defect in ribosome assembly and resulting growth phenotype of the mutant could be restored by expression of wild-type RluD and synthesis of Psi1911, Psi1915, and Psi1917 residues, but not by catalytically inactive mutant RluD proteins, incapable of pseudouridine formation. The data suggest that the loss of the pseudouridine residues can account for all aspects of the mutant phenotype; however, a possible second function of the RluD synthase is also discussed.     

Ultrastructural alterations in rat brain tissues under the direct action of Escherichia coli endotoxin]

The experiments on the rats with intracisternal injection of endotoxin have revealed essential differences in the mechanisms of its permeability through cerebrospinal fluid-brain and blood-cerebrospinal fluid barriers. As for ependymal cells, endotoxin shunts through the cytoplasm in the areas of tight junctions and then it reaches perineuronal spaces. The mechanism of endotoxin penetration through the epithelium of choroid plexi is associated with receptor-mediated endocytosis.