A transmembranous NADH-dehydrogenase in human erythrocyte membranes

Evidence is presented for a transmembranous NADH-dehydrogenase in human erythrocyte plasma membrane. We suggest that this enzyme is responsible for the ferricyanide reduction by intact cells. This NADH-dehydrogenase is distinctly different from the NADH-cytochromeb ₅ reductase on the cytoplasmic side of the membrane. Pretreatment of erythrocytes with the nonpenetrating inhibitor diazobenzene sulfonate (DABS) results in a 35% loss of NADH-ferricyanide reductase activity in the isolated plasma membrane. Since NADH and ferricyanide are both impermeable, the transmembrane enzyme can only be assayed in open membrane sheets with both surfaces exposed, and not in closed vesicles. The transmembrane dehydrogenase has affinity constants of 90 µM for NADH and 125 µM for ferricyanide. It is inhibited byp-chloromercuribenzoate, bathophenanthroline sulfonate, and chlorpromazine.     

Deficiency of Pten accelerates mammary oncogenesis in MMTV-Wnt-1 transgenic mice

Background  

Germline mutations in the tumor suppressor PTEN predispose human beings to breast cancer, and genetic and epigenetic alterations of PTEN are also detected in sporadic human breast cancer. Germline Pten mutations in mice lead to the development of a variety of tumors, but mammary carcinomas are infrequently found, especially in mice under the age of six months.     

Papaver bracteatum,potential commercial source of codeine

Papaver bracteatum, native to Iran and southern Russia, has been grown successfully in many countries. Research in the northwest United States has confirmed the potential for its commercial production as a source of the alkaloid thebaine. Potential for the chemical conversion of thebaine into codeine, one of man’s most widely used alkaloidal medicinal agents, is reviewed. Economic and social advantages of growing this species over opium poppy (Papaver somniferum) are discussed. The value of the seed oil for cooking and industrial use is considered.     

Friends of mine: An invasive freshwater mussel facilitates growth of invasive macrophytes and mediates their competitive interactions

1. Increasing rates of invasions in ecosystems worldwide necessitate experiments to determine the role of biotic interactions in the success and impact of multiple alien species. Here, we examined competitive and facilitative interactions among various combinations of three widespread and often co-occurring invaders: the zebra mussel Dreissena polymorpha, and the macrophytes Elodea canadensis and Elodea nuttallii.
2. Using a mesocosm-based, factorial experimental design, we assessed the effect of interspecific competition on macrophyte growth rates in the absence and presence at varying biomass of D. polymorpha.
3. Growth rates (wet g/day) of E. canadensis and E. nuttallii were similar when grown in isolation. When grown together, in the absence of D. polymorpha, E. canadensis growth was not significantly reduced in the presence of E. nuttallii and vice versa. In the presence of D. polymorpha (26.0 ± 1 mm), monocultural growth of E. canadensis was largely unaffected, while E. nuttallii growth was strongly enhanced. Low (2.64 g) and medium (3.96 g) mussel biomass led to negative interspecific effects between E. canadensis and E. nuttallii; at high (5.28 g) mussel biomass, the effect of interspecific competition was negated.
4. Overall, D. polymorpha alleviated competitive interactions between the two invasive macrophytes when all three species co-occurred, and substantially enhanced growth of E. nuttallii with increasing mussel biomass, thereby suggesting a possible influence on the relative dominance of these macrophytes in the field.
5. Our study demonstrates how facilitations can cause shifts in dominance among closely related invaders. The consequences of such facilitations for the structure and function of communities remain to be explored generally.

     

Affinity chromatography purification of penicillinase of Bacillus licheniformis 749-C and its use to measure tuurnover of the cell bound enzyme

Affinity chromatography purification of small amounts of penicillinase using cephalosporin C covalently linked to Sepharose 4B has been used in examining the turnover of cell-bound penicillinase by B. licheniformis 749/C. Under conditions in which most of the nascent penicillinase is retained by the cells, turnover could be demonstrated (15% of the cell-bound enzyme in 2.5 hours), although most of the secreted enzyme is derived from newly-formed molecules.     

New functions for coenzyme Q

Summary Coenzyme Q is primarily identified with its role in energy coupling where it is involved in the generation of a proton gradient across membranes to drive ATP formation. Its identification as a significant antioxidant throughout cellular membranes is developing. Its function in other membrane redox systems introduces new functions such as the generation of hydrogen peroxide related to cellular signal systems or the acidification of other organelles. A role in the control of cell growth and apoptosis has also been introduced.     

A study of intestinal copper-binding proteins in mottled mice

The substantial retention of Cu2+ and to a lesser extent Zn2+, in the gut mucosa of neonatal MO mutant mice is largely associated with a low molecular weight protein tentatively identified as metallothionein. [35S]Cysteine incorporation into this protein in mutant mice is elevated, indicating that Cu2+ retention in the gut is associated with an increase in the synthesis of metallothionein. The high Cu2+ levels of mutant gut tissue decline rapidly with age to reach an approximately normal level by 24 days of age; this decline cannot be prevented by dietary supplementation and it is suggested that gut 'closure' and consequent reduced uptake by pinocytosis are important factors in this decline.     

Quantitative and kinetic examination of 32P-postlabeling of etheno-substituted nucleotides

1,N6-ethenodeoxyadenosine-, 1,N2-ethenodeoxyguanosine- and 3,N4-ethenodeoxycytidine-3'-monophosphates were labeled by [gamma-32P] ATP using T4 polynucleotide kinase in conditions commonly used for the 32P-postlabeling assay. Kinetic studies showed that the reaction is fast reaching a plateau after 15-30 min. The efficiency of phosphorylation, as studied by substrate-product concentration dependency, was between 50-100% at the lower substrate concentrations. The adducts are labeled efficiently at sub-femtomole levels. All the adducts were sensitive to the 3'-dephosphorylation by P1 nuclease although the guanine derivative appeared to be more resistant than the two other adducts.