Osmotic Regulation and the Biosynthesis of Membrane-Derived Oligosaccharides in Escherichia coli
The membrane-derived oligosaccharides (MDO) of Escherichia coli are periplasmic constituents containing 8--10 glucose units in a highly branched structure, linked by β 1-2 and β 1--6 bonds [Schneider, J. E., Reinhold, V., Rumley, M. K. & Kennedy, E. P. (1979) J. Biol. Chem. 254, 10135--10138]. T...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1982-02, Vol.79 (4), p.1092-1095 |
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description | The membrane-derived oligosaccharides (MDO) of Escherichia coli are periplasmic constituents containing 8--10 glucose units in a highly branched structure, linked by β 1-2 and β 1--6 bonds [Schneider, J. E., Reinhold, V., Rumley, M. K. & Kennedy, E. P. (1979) J. Biol. Chem. 254, 10135--10138]. The MDO are multiply substituted with sn-1-phosphoglycerol residues (derived from membrane phosphatidylglycerol) and with O-succinyl ester residues and, thus, are highly anionic. Experiments in this paper offer evidence that the biosynthesis of MDO is an important aspect of osmoregulation in E. coli. Cells grown in medium of low osmolarity (ca. 50 mosM) synthesize 16 times more MDO than those grown in the same medium with 0.4 M NaCl. In cells grown in medium of low osmolarity, it appears that MDO is the principal source of fixed anion in the periplasmic space and, thus, acts to maintain the high osmotic pressure and Donnan membrane potential of the periplasmic compartment. Regulation of MDO synthesis in response to changes in osmolarity of the medium appears to occur at the genetic level because the synthesis of new protein is needed to permit the production of MDO at high rates after shift of cells to medium of low osmolarity. |
doi_str_mv | 10.1073/pnas.79.4.1092 |
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E., Reinhold, V., Rumley, M. K. & Kennedy, E. P. (1979) J. Biol. Chem. 254, 10135--10138]. The MDO are multiply substituted with sn-1-phosphoglycerol residues (derived from membrane phosphatidylglycerol) and with O-succinyl ester residues and, thus, are highly anionic. Experiments in this paper offer evidence that the biosynthesis of MDO is an important aspect of osmoregulation in E. coli. Cells grown in medium of low osmolarity (ca. 50 mosM) synthesize 16 times more MDO than those grown in the same medium with 0.4 M NaCl. In cells grown in medium of low osmolarity, it appears that MDO is the principal source of fixed anion in the periplasmic space and, thus, acts to maintain the high osmotic pressure and Donnan membrane potential of the periplasmic compartment. Regulation of MDO synthesis in response to changes in osmolarity of the medium appears to occur at the genetic level because the synthesis of new protein is needed to permit the production of MDO at high rates after shift of cells to medium of low osmolarity.</description><subject>Anions</subject><subject>Bacterial Proteins - biosynthesis</subject><subject>Cell growth</subject><subject>Cell Membrane - metabolism</subject><subject>Culture Media</subject><subject>Cultured cells</subject><subject>Cytoplasm</subject><subject>Escherichia coli</subject><subject>Escherichia coli - metabolism</subject><subject>Gene expression regulation</subject><subject>oligosaccharides</subject><subject>Oligosaccharides - biosynthesis</subject><subject>Osmolar Concentration</subject><subject>Osmoregulation</subject><subject>osmosis</subject><subject>P branes</subject><subject>Periplasm</subject><subject>Physiological regulation</subject><subject>Pyridines</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9vFCEcxYmxqWv16sHEhFNvswLDj-HgwdZqTWo2MfZMGQZ2aJhhhZnG_vey2c26vdjTF_I-D943D4B3GC0xEvXHzajzUsglLVdJXoBFGbjiVKKXYIEQEVVDCX0FXud8jxCSrEGn4FQgijGuF-BulYc4eQN_2vUc9OTjCPXYwam38MLH_DiWU_YZRgd_2KFNerTVF5v8g-3gKvh1zNqYXiff2Qz9CK-y6Ytseq-hicG_ASdOh2zf7ucZuP169evyurpZfft--fmmMozVU0XarkQWnHDHGG-Z5ZRJ7Sh12HJMHKGOtVYSWWtEtBG87WraIWepbETjRH0GPu3e3cztYDtjxynpoDbJDzo9qqi9eqqMvlfr-KDq8hHixX--96f4e7Z5UoPPxoZQFo5zVoIiIXAjnwVxzSTHTVPA5Q40KeacrDuEwUhtu1Pb7pSQiqptd8Xw4XiFA74v60jf-g7qkf_8f7pycwiT_TMV8P0OvM9TTP9iYdmw-i_kibeQ</recordid><startdate>19820201</startdate><enddate>19820201</enddate><creator>Kennedy, Eugene P.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19820201</creationdate><title>Osmotic Regulation and the Biosynthesis of Membrane-Derived Oligosaccharides in Escherichia coli</title><author>Kennedy, Eugene P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c553t-2bd4907626f556b5e6459af44f1e612f24f5be9293a02ac76bd34d0fe49878f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Anions</topic><topic>Bacterial Proteins - biosynthesis</topic><topic>Cell growth</topic><topic>Cell Membrane - metabolism</topic><topic>Culture Media</topic><topic>Cultured cells</topic><topic>Cytoplasm</topic><topic>Escherichia coli</topic><topic>Escherichia coli - metabolism</topic><topic>Gene expression regulation</topic><topic>oligosaccharides</topic><topic>Oligosaccharides - biosynthesis</topic><topic>Osmolar Concentration</topic><topic>Osmoregulation</topic><topic>osmosis</topic><topic>P branes</topic><topic>Periplasm</topic><topic>Physiological regulation</topic><topic>Pyridines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kennedy, Eugene P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kennedy, Eugene P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osmotic Regulation and the Biosynthesis of Membrane-Derived Oligosaccharides in Escherichia coli</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1982-02-01</date><risdate>1982</risdate><volume>79</volume><issue>4</issue><spage>1092</spage><epage>1095</epage><pages>1092-1095</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The membrane-derived oligosaccharides (MDO) of Escherichia coli are periplasmic constituents containing 8--10 glucose units in a highly branched structure, linked by β 1-2 and β 1--6 bonds [Schneider, J. E., Reinhold, V., Rumley, M. K. & Kennedy, E. P. (1979) J. Biol. Chem. 254, 10135--10138]. The MDO are multiply substituted with sn-1-phosphoglycerol residues (derived from membrane phosphatidylglycerol) and with O-succinyl ester residues and, thus, are highly anionic. Experiments in this paper offer evidence that the biosynthesis of MDO is an important aspect of osmoregulation in E. coli. Cells grown in medium of low osmolarity (ca. 50 mosM) synthesize 16 times more MDO than those grown in the same medium with 0.4 M NaCl. In cells grown in medium of low osmolarity, it appears that MDO is the principal source of fixed anion in the periplasmic space and, thus, acts to maintain the high osmotic pressure and Donnan membrane potential of the periplasmic compartment. 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subjects | Anions Bacterial Proteins - biosynthesis Cell growth Cell Membrane - metabolism Culture Media Cultured cells Cytoplasm Escherichia coli Escherichia coli - metabolism Gene expression regulation oligosaccharides Oligosaccharides - biosynthesis Osmolar Concentration Osmoregulation osmosis P branes Periplasm Physiological regulation Pyridines |
title | Osmotic Regulation and the Biosynthesis of Membrane-Derived Oligosaccharides in Escherichia coli |
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