1932

Abstract

Mary Osborn was a native Californian. She was an undergraduate at the University of California, Berkeley, where she worked in the laboratory of I.L. Chaikoff. She received her PhD at the University of Washington, where her work on the role of folic acid coenzymes in one-carbon metabolism revealed the mechanism of action of methotrexate. After postdoctoral training with Bernard Horecker in the Department of Microbiology at New York University (NYU), she embarked on her research career as a faculty member in the NYU Department of Microbiology and in the Department of Molecular Biology at Albert Einstein College of Medicine. In 1968 she moved as one of the founding faculty of the new medical school of the University of Connecticut, where she remained until her retirement in 2014. Her research was focused on the biosynthesis of the endotoxin lipopolysaccharide (LPS) of gram-negative bacteria and on the assembly of the bacterial cell envelope. She made seminal contributions in these areas. She was the recipient of numerous honors and served as president of several important scientific organizations. Later in her career she served as chair of the National Research Council Committee on Space Biology and Medicine, advisory to the National Aeronautics and Space Administration (NASA), which produced an influential report that plotted the path for NASA's space biology research program in the first decade of the twenty-first century. Dr. Osborn died on Jan. 17, 2019.

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2019-09-08
2024-04-24
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Literature Cited

  1. 1. 
    Anderson J, Matruhashi M, Haskin M, Strominger J 1965. Lipid-phosphoacetylmuramyl-pentapeptide and lipid-phosphodisaccharide-pentapeptide: presumed membrane transport intermediates in cell wall synthesis. PNAS 53:881–89
    [Google Scholar]
  2. 2. 
    Bayer ME. 1967. Response of cell walls of Escherichia coli to a sudden reduction in the environmental osmotic pressure. J. Bacteriol. 93:1104–10
    [Google Scholar]
  3. 3. 
    Bayer ME. 1968. Areas of adhesion between wall and membrane of Escherichia coli. J. Gen. Microbiol. 53:395–404
    [Google Scholar]
  4. 4. 
    Chung J-S, Gronenberg L, Kahne D 2010. Proteins required for lipopolysaccharide assembly in Escherichia coli form a transenvelope complex. Biochemistry 49:4565–67
    [Google Scholar]
  5. 5. 
    Eidels L, Osborn M. 1971. Aldoheptose and lipopolysaccharide biosynthesis in transketolase mutants of Salmonella typhimurium. PNAS 68:1673–77
    [Google Scholar]
  6. 6. 
    Heath E, Ghalambor M. 1963. 2-Keto-3-deoxy-octonate, a constituent of cell wall lipopolysaccharide preparations obtained from Escherichia coli. Biochem. Biophys. Res. Commun 10:340
    [Google Scholar]
  7. 7. 
    Higashi Y, Strominger J, Sweeley C 1967. Structure of a lipid intermediate in cell wall peptidoglycan synthesis: a derivative of a C55 isoprenoid alcohol. PNAS 57:1878–84
    [Google Scholar]
  8. 8. 
    Ishidate K, Creeger E, Zrike J, Deb S, Glauner B et al. 1986. Isolation of differentiated membrane domains from Escherichia coli and Salmonella typhimurium, including a fraction containing attachment sites between the inner and outer membranes and the murein skeleton of the cell envelope. J. Biol. Chem. 261:428–43
    [Google Scholar]
  9. 9. 
    Islam S, Eckford P, Jones M, Nugent T, Bear C et al. 2013. Proton gating and proton-dependent uptake by Wzx support O-antigen subunit antiport across the bacterial inner membrane. mBio 4:e00678–13
    [Google Scholar]
  10. 10. 
    Jones N, Osborn M. 1977. Translocation of phospholipids between the outer and inner membranes of Salmonella typhimurium. J. Biol. Chem. 252:7405–12
    [Google Scholar]
  11. 11. 
    Kent J, Osborn M. 1968. Haptenic O-antigen as a polymeric intermediate of in vivo synthesis of lipopolysaccharide by Salmonella typhimurium. Biochemistry 7:4419–25
    [Google Scholar]
  12. 12. 
    Konovalova A, Kahne D, Silhavy T 2017. Outer membrane biogenesis. Annu. Rev. Microbiol. 71:539–56
    [Google Scholar]
  13. 13. 
    Liu D, Cole R, Reeves P 1996. An O-antigen processing function for Wzx (RfbX): a promising candidate for O-unit flippase. J. Bacteriol. 178:2102–7
    [Google Scholar]
  14. 14. 
    Marino P, McGrath B, Osborn M 1991. Energy dependence of O-antigen synthesis in Salmonella typhimurium. J. Bacteriol. 173:3128–33
    [Google Scholar]
  15. 15. 
    Marino P, Phan K, Osborn M 1985. Energy dependence of lipopolysaccharide translocation in Salmonella typhimurium. J. Biol. Chem. 260:4965–70
    [Google Scholar]
  16. 16. 
    Mulford C, Osborn M. 1983. An intermediate step in the translocation of lipopolysaccharide to the outer membrane of Salmonella typhimurium. PNAS 80:159–63
    [Google Scholar]
  17. 17. 
    Munson R, Rasmussen N, Osborn M 1978. Incorporation of 3-deoxy-d-mannooctulosonate into a precursor of lipid A in Salmonella typhimurium. J. Biol. Chem. 253:1503–10
    [Google Scholar]
  18. 18. 
    Nikaido H. 1962. On the biosynthesis of lipopolysaccharide in mutant strains of Salmonella. PNAS 48:1542–48
    [Google Scholar]
  19. 19. 
    Nikaido H. 1962. Studies on the biosynthesis of lipopolysaccharide in mutant strains of Salmonella. PNAS 48:1337–41
    [Google Scholar]
  20. 20. 
    Okuda S, Sherman D, Silhavy T, Ruiz N, Kahne D 2016. Lipopolysaccharide transport and assembly at the outer membrane: the PEZ model. Nat. Rev. Microbiol. 14:337–45
    [Google Scholar]
  21. 21. 
    Osborn M. 1963. Studies on the Gram-negative cell wall. I. Evidence for the role of 2-keto-3-deoxyoctulosonate in the lipopolysaccharide of Salmonella typhimurium. PNAS 50:499–505
    [Google Scholar]
  22. 22. 
    Osborn M, Freeman M, Huennekens F 1958. Inhibition of dihydrofolic reductase by aminopterin and amethopterin. Proc. Soc. Exp. Biol. Med. 97:429–31
    [Google Scholar]
  23. 23. 
    Osborn M, Gander J, Parisi E, Carson J 1972. Mechanism of assembly of the outer membrane of Salmonella typhimurium: isolation and characterization of the cytoplasmic and outer membrane. J. Biol. Chem. 247:3962–72
    [Google Scholar]
  24. 24. 
    Osborn M, Rosen S, Rothfield L, Horecker B 1962. Bacterial lipopolysaccharide. I. Enzymatic incorporation of galactose in a mutant strain of Salmonella. PNAS 48:1831–38
    [Google Scholar]
  25. 25. 
    Osborn M, Rosen S, Rothfield L, Zeleznick L, Horecker B 1964. Lipopolysaccharide of the Gram negative cell wall. Science 145:783–89
    [Google Scholar]
  26. 26. 
    Reichard P. 1968. The biosynthesis of deoxyribonucleotides. Eur. J. Biochem. 3:259–66
    [Google Scholar]
  27. 27. 
    Rick P, Osborn M. 1972. Isolation of a mutant of Salmonella typhimurium dependent on d-arabinose-5-phosphate for growth and synthesis of 3-deoxy-d-mannoctulosonate (ketodeoxyoctonate). PNAS 69:3756–60
    [Google Scholar]
  28. 28. 
    Rick P, Osborn M. 1977. Lipid A mutants of Salmonella typhimurium: characterization of a conditional lethal mutant in 3-deoxy-d-mannooctulosonate. J. Biol. Chem. 252:4893–902
    [Google Scholar]
  29. 29. 
    Rothfield L, Osborn M, Horecker B 1964. Biosynthesis of bacterial lipopolysaccharide. II. Incorporation of glucose and galactose catalyzed by particulate and soluble enzymes in Salmonella. J. Biol. Chem. 239:2788–95
    [Google Scholar]
  30. 30. 
    Rothfield L, Pearlman-Kothencz M. 1969. Synthesis and assembly of bacterial membrane components: a lipopolysaccharide-phospholipid-protein complex excreted by living bacteria. J. Mol. Biol. 44:477–92
    [Google Scholar]
  31. 31. 
    Silhavy T, Kahne D, Walker S 2010. The bacterial cell envelope. Cold Spring Harb. Perspect. Biol. 2:a000414
    [Google Scholar]
  32. 32. 
    Sutherland I, Luderitz O, Westphal O 1965. Studies on the structure of lipopolysaccharides of Salmonella minnesota and Salmonella typhimurium R strains. Biochem. J. 96:439–48
    [Google Scholar]
  33. 33. 
    Weber K, Osborn M. 1969. The reliability of molecular weight determination by dodecyl sulfate-polyacrylamide gel electrophoresis. J. Biol. Chem. 244:4406–12
    [Google Scholar]
  34. 34. 
    Weiner I, Higuchi T, Rothfield L, Saltmarsh-Andrew M, Osborn M, Horecker B 1965. Biosynthesis of bacterial lipopolysaccharide. V. Lipid-linked intermediates in the biosynthesis of the O-antigen groups of Salmonella typhimurium. PNAS 54:228–35
    [Google Scholar]
  35. 35. 
    Whitfield C, Trent MS. 2014. Biosynthesis and export of bacterial lipopolysaccharide. Annu. Rev. Biochem. 83:99–128
    [Google Scholar]
  36. 36. 
    Wright A, Dankert A, Fennessey M, Robbins P 1967. Characterization of a polyisoprenoid compound functional in O-antigen synthesis. PNAS 57:1798–803
    [Google Scholar]
  37. 37. 
    Wright A, Dankert M, Robbins P 1965. Evidence for an intermediate stage in the biosynthesis of the Salmonella O-antigen. PNAS 54:235–42
    [Google Scholar]
  38. 38. 
    Zeleznick L, Rosen S, Saltmarsh-Andrew M, Osborn M, Horecker B 1965. Biosynthesis of bacterial lipopolysaccharide. IV. Enzymatic incorporation of mannose, rhamnose and galactose in a mutant strain of Salmonella typhimurium. PNAS 53:207–14
    [Google Scholar]
  39. 39. 
    Zhou Z, White K, Polissi A, Georgopoulos G, Raetz C 1998. Function of Escherichia coli MsbA, an essential ABC family transporter in lipid A and phospholipid synthesis. J. Biol. Chem. 273:12466–75
    [Google Scholar]
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