Inhibition of growth of the green algaChlorella pyrenoidosa by unsaturated fatty acids

The activity of a number of unsaturated fatty acids in inhibiting the growth of the green algaChlorella pyrenoidosa has been studied using the paper disk-agar plate method. Acrylic and undecylenic acids were highly active, but other θ-unsaturated fatty acids tested were only weakly active. Oleic and elaidic acids were inactive at 0.2 M, but other C₁₈-C₂₂ acids with 2 to 6 double bonds were generally active down to a concentration of 0.01–0.005 M. Activity with chaulmoogric acid was noted down at 0.002–0.001 M. Diffusion rates of the acids through the agar seem to affect the size of the inhibition zones. The implications that polyunsaturated fatty acids may play a role in algal ecology are discussed.     

Prostacyclin analog-suppressed ischemia-reperfusion injury of the rat liver: evaluation by calpain mu activation

Advances in perinatal and neonatal health care over the past few decades have resulted in a substantial reduction in perinatal mortality. Some of this improvement has been attributed to antepartum fetal surveillance techniques. The primary objective of antepartum fetal surveillance techniques is to avoid fetal deaths. An ideal secondary objective is to avoid neonatal complications related to intrauterine asphyxia. In this article, some of the difficulties in evaluating existing antepartum fetal surveillance techniques are highlighted. Some of the epidemiological methods for evaluating a screening test are reviewed and their importance discussed with reference to fetal testing procedures. Lastly, the possibility of considering indication-specific fetal testing to improve perinatal morbidity is examined.     

Prospective study of the detection of anomalous connections of pancreatobiliary ducts during routine medical examinations

BACKGROUND/AIMS: It is important to achieve detection of of anomalous connections of the pancreatobiliary ducts (ACPBD), because this condition often leads to pancreatobiliary disease. The present prospective investigation focused on revealing the incidence of ACPBD in asymptomatic individuals undergoing medical checkups. MATERIAL AND METHODS: Extracorporeal ultrasonography (US) was performed on all asymptomatic individuals undergoing medical checkups. Identification by abdominal ultrasonography of 3 mm or more gallbladder wall thickening, or 10 mm or more dilatation of the bile duct were considered indicative of ACPBD and endoscopic ultrasonography (EUS) was carried out in selected cases. Endoscopic retrograde cholangiopancreatography (ERCP) was then performed to confirm the existence of ACPBD. RESULTS: The overall incidence of ACPBD was 0.03% (9/27,076 subjects). ACPBD was found in 23% of cases with bile duct dilatation, and in 2.9% with gallbladder wall thickening. CONCLUSION: ACPBD was not as rare a disease as expected. For early detection of ACPBD, identification by abdominal ultrasonography of gallbladder wall thickening or dilatation of the bile duct are indicative. Patients who are suspected of having this abnormality should then undergo EUS. The final diagnosis should then be made by ERCP.     

A 32 kbyte integrated cache memory

The system, circuit, layout and device levels of an integrated cache memory (ICM), which includes 32 kbyte DATA memory with typical address to HIT delay of 18 ns and address to DATA delay of 23 ns, are described. The ICM offers the largest memory size and the fastest speed ever reported in a cache memory. The device integrates a 32 kbyte DATA INSTRUCTION memory, a 34 kbit TAG memory, an 8 kbit VALID flat, a 2 kbit least recently used (LRU) flag, comparators, and CPU interface logic circuits on a chip. The inclusion of the DATA memory is crucial in improving system cycle time. The device uses several novel circuit design technologies, including a double-word-line scheme, low-noise flush clear, a low-power comparator, noise immunity, and directly testable memory design. Its newly proposed way-slice architecture increases both flexibility and expandability     

Electron diffraction study of aging processes in Fe-1.83 wt pct C martensite at room temperature

Aging processes occurring in an Fe-1.83 wt pct C martensite at room temperature have been studied by electron diffraction, assisted by transmission electron microscopy observation. Fourier analysis of diffuse scattering from the martensite suggested that a spinodal decomposition occurred therein. The spinodally modulated microstructure was composed of a dominant wave with a wavelength of about 1 nm and nondominant waves with longer wavelengths and was observed not to grow even after aging for several months. The reason for the nongrowth may be that the coarsening was stopped by strong elastic interactions between carbon-enriched and carbon-depleted regions. Furthermore, the tetragonality of the martensite was observed to remain constant during aging, suggesting that carbon redistribution during spinodal decomposition occurred within one set of the octahedral interstitial sitesO _z only. formerly Visiting Researcher, The Institute of Scientific and Industrial Research, Osaka University     

Characterization of the hemorrhagic reaction caused by Vibrio vulnificus metalloprotease, a member of the thermolysin family

Vibrio vulnificus is an opportunistic human pathogen causing wound infections and septicemia, characterized by hemorrhagic and edematous damage to the skin. This human pathogen secretes a metalloprotease (V. vulnificus protease [VVP]) as an important virulence determinant. When several bacterial metalloproteases including VVP were injected intradermally into dorsal skin, VVP showed the greatest hemorrhagic activity. The level of the in vivo hemorrhagic activity of the bacterial metalloproteases was significantly correlated with that of the in vitro proteolytic activity for the reconstituted basement membrane gel. Of two major basement membrane components (laminin and type IV collagen), only type IV collagen was easily digested by VVP. Additionally, the immunoglobulin G antibody against type IV collagen, but not against laminin, showed sufficient protection against the hemorrhagic reaction caused by VVP. Capillary vessels are known to be stabilized by binding of the basal surface of vascular endothelial cells to the basement membrane. Therefore, specific degradation of type IV collagen may cause destruction of the basement membrane, breakdown of capillary vessels, and leakage of blood components including erythrocytes.     

Characterization and functional role of the QH site of bo-type ubiquinol oxidase from Escherichia coli

Cytochrome bo is a four-subunit terminal ubiquinol oxidase in the aerobic respiratory chain of Escherichia coli that vectorially translocates protons not only via directed protolytic reactions but also via proton pumping. Previously, we postulated that a bound quinone in the high-affinity quinone binding site (QH) mediates electron transfer from the low-affinity quinol oxidation site (QL) in subunit II to low-spin heme b in subunit I as an electron gate and a transient electron reservoir [Sato-Watanabe, M., Mogi, T., Ogura, T., Kitagawa, T., Miyoshi, H., Iwamura, H., and Anraku, Y. (1994b) J. Biol. Chem. 269, 28908-28912]. In the present study, we carried out screening of ubiquinone analogues using a bound ubiquinone-free enzyme (DeltaUbiA1) that has been isolated from a ubiquinone biosynthesis mutant, and identified PC24 (2-chloro-4, 6-dinitrophenol), PC32 (2,6-dibromo-4-cyanophenol), and PC52 (2-isopropyl-5-methyl-4,6-dinitrophenol) as potent QH site inhibitors. PC15 (2,6-dichloro-4-nitrophenol) and PC16 (2, 6-dichloro-4-dicyanovinylphenol), potent QL site inhibitors, did not exhibit such a selective inhibition of the QH site. Binding studies using the air-oxidized DeltaUbiA enzyme showed that PC32 and PC52 have 4- to 7-fold higher affinity than ubiquinone-1. Reconstitution of the QH site with PC32 and PC52 resulted in a decrease of the apparent Vmax value to 1/7 and 1/3, respectively, of the control activity. These findings suggest that structural features of the QL and QH sites are different, and provide further support for the involvement of the QH site in intramolecular electron transfer and facile oxidation of quinols at the QL site.