Hepes may stimulate cultured endothelial cells to make growth-retarding oxygen metabolites

Summary Zwitterion buffers are often used to modulate the pH of cell culture medium but their effect on cultured cells is controversial. We found that addition of 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) caused superoxide dismutase (SOD) inhibitable increases in nitroblue tetrazolium dye reduction and SOD and catalase inhibitable decreases in the growth of cultured bovine pulmonary artery endothelial cells. The findings suggest that HEPES stimulates endothelial cells to make toxic oxygen metabolites that contribute to decreased cell growth. This work was supported in part by the National Institutes of Health, Colorado and American Lung Associations, Colorado and American Heart Associations, the Council for Tobacco Research, and the Kroc, Hill, Swan and Kleberg Foundations. Dr. Bowman is a Clinician Scientist Awardee of the American Heart Association.     

Chromosomal localization of group-specific component by in situ hybridization

Group-specific component (GC), an alpha 2-globulin plasma protein synthesized primarily in the liver, is the major vitamin D-binding protein in plasma. It has two common phenotypes, GC1 and GC2, which appear in all human populations. Using the cDNA insert containing the entire coding sequence of GC2, the GC gene was mapped to human chromosomal bands 4q13----q21.1 by in situ hybridization.     

Heliobacterium chlorum: cell organization and structure

The basic cellular organization of Heliobacterium chlorum is described using the freeze-etching technique. Internal cell membranes have not been observed in most cells, leading to the conclusion that the photosynthetic apparatus of these organisms must be localized in the cell membrane of the bacterium. The two fracture faces of the cell membrane are markedly different. The cytoplasmic (PF) face is covered with densely packed particles averaging 8 nm in diameter, while the exoplasmic (EF) face contains far fewer particles, averaging approximately 10 nm in diameter. Although a few differentiated regions were noted within these fracture faces, the overall appearance of the cell membrane was remarkably uniform. The Heliobacterium chlorum cell wall is a strikingly regular structure, composed of repeating subunits arranged in a rectangular pattern at a spacing of 11 nm in either direction. We have isolated cell wall fragments by brief sonication in distilled water, and visualized the cell wall structure by negative staining as well as deep-etching.Abbreviations PF protoplasmic fracture face - EF exoplasmic fracture face     

Selective inhibition of the potato scab pathogen by antagonistic bacteria and substrate influence on antibiotic production

Summary In a long-term field experiment a soybean cover crop and green manure incorporation prevented the build-up of common scab of potato whereas barley, employed in the same manner, increased disease incidence. When soil from these plots was assayed for organisms antagonistic toS. scabies, a bacterium indentified asBacillus subtilis, was found to be predominant. Laboratory tests showed thatS. scabies was more sensitive to the antibiotic produced by this bacterium than most non-pathogenicStreptomyces spp which were tested. The antibiotic was found to be similar to bacitracin and activity was expressed as units bacitracin. Water extracts of greenhouse-grown soybean and barley were compared, at different concentrations, as a substrate for growth and antibiotic production by this bacterium. It was found that on the soybean extract, antibiotic activity, as measured by the standard filter-paper-disc technique, was 2.5 to 3 times greater per unit of bacterial growth than when barley extract was used as the substrate. Similar results were obtained when extracts of partially decomposed tissue were used. It is suggested that when evaluating antagonistic organisms as a possible factor in the behavior of plant pathogens in soil, the relative sensitivity of the pathogen to the antibiotic activities of the antagonists as well as the substrates available to the antagonists should be considered.