Antitumor Lipopolysaccharide from Heptoseless Mutant of Proteus mirabilis |
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Authors: | Masaki Nakahara Nobuaki Kitahara Kiyoshi Hamano Mamoru Arat Hiroshi Okazaki |
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Affiliation: | Fermentation Research Laboratories, Sankyo Co., Ltd., No. 2-58, Hiromachi 1-chome, Shinagawa-ku, Tokyo 140, Japan |
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Abstract: | Studies on lipopolysaccharide (LPS) from the cells of Proteus mirabilis RMS-203 were focused upon reduction of lethal toxicity and of pyrogenicity by biological and chemical modification. A heptoseless mutant, strain N-434, was isolated by the use of phage resistancy as a tool. LPS from that heptoseless mutant was completely deficient in neutral sugars and mainly composed of 2-keto-deoxy-octonic acid (KDO), glucosamine and fatty acids. It revealed almost the same antitumor activity as LPS of the wild type but it was less toxic and less pyrogenic.Hydroxylaminolysis and reduction with LiAlH4 resulted in removal of fatty acids from LPS accompanied with decrease in lethal toxicity and antitumor acitivity but not in pyrogenicity.Lipid A fractions showed almost the same antitumor activity as intact LPS but less lethality and less pyrogenicity. |
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Keywords: | α- smallcaps smallerCapital" >D-glucosylglycerol enzymatic synthesis characteristics α-glucosidase batch method |
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