Surfactin inhibits the growth of Propionibacterium acnes by destroying the cell wall and membrane

Author(s):  
M.Y. Shan ◽  
F.Q. Meng ◽  
L.B. Zhou ◽  
F.X. Lu ◽  
X.M. Bie ◽  
...  
1985 ◽  
Vol 97 (6) ◽  
pp. 1669-1678 ◽  
Author(s):  
Masato NAGAOKA ◽  
Kei-ichi KAMISANGO ◽  
Hideji FUJII ◽  
Kei-ichi UCHIKAWA ◽  
Isao SEKIKAWA ◽  
...  

1990 ◽  
Vol 45 (7-8) ◽  
pp. 797-804
Author(s):  
Mary Fran Verostek ◽  
Lee E. Bartholomew ◽  
Peter Weber

Abstract An acid-labile antigenic polysaccharide has been isolated from both cell walls and culture media of Propionibacterium acnes using a new chemical degradation procedure which liberates protein-bound or associated carbohydrate. Lyophilized cells and culture media were treated with a suspension of mercuric oxide in a solution of alkaline mercuric cyanide for several hours at room temperature liberating water-soluble polysaccharide material. The antigenic polysac- charide was freed of reaction products by alcohol extraction and purified by anion exchange chromatography and gel filtration, resulting in three distinct fractions of acidic polysaccha- rides of apparent molecular weights between 15 - 50 kDa. Sugar analysis showed the polysac- charides to contain fucose, galactose, glucose, mannose, galactosamine. glucosamine, and 2,3- diamino-2.3-dideoxy-D-glucuronic acid. The three fractions also contained amino acids, predominantly glutamic acid, alanine, and glycine, known to be components of P. acnes cell wall peptidoglycan. All three molecular weight fractions reacted with rabbit antisera raised against whole P. acnes cells, with the highest titer for both cell and media-derived polysaccharide material consistently in the high molecular weight fraction. This procedure was also capable of releasing antigenic polysaccharide from tissues of rats administered P. acnes cells or radio- labeled cell wall fragments.


1990 ◽  
Vol 13 (2) ◽  
pp. 136-141
Author(s):  
Yasuhiro Mizoguchi ◽  
Hiroshi Kuboi ◽  
Shuichi Seki ◽  
Kenzo Kobayashi ◽  
Sukeo Yamamoto ◽  
...  

1985 ◽  
Vol 84 (6) ◽  
pp. 496-500 ◽  
Author(s):  
Guy F. Webster ◽  
Jeffrey P. Indrisano ◽  
James J. Leyden

1997 ◽  
Vol 161 ◽  
pp. 491-504 ◽  
Author(s):  
Frances Westall

AbstractThe oldest cell-like structures on Earth are preserved in silicified lagoonal, shallow sea or hydrothermal sediments, such as some Archean formations in Western Australia and South Africa. Previous studies concentrated on the search for organic fossils in Archean rocks. Observations of silicified bacteria (as silica minerals) are scarce for both the Precambrian and the Phanerozoic, but reports of mineral bacteria finds, in general, are increasing. The problems associated with the identification of authentic fossil bacteria and, if possible, closer identification of bacteria type can, in part, be overcome by experimental fossilisation studies. These have shown that not all bacteria fossilise in the same way and, indeed, some seem to be very resistent to fossilisation. This paper deals with a transmission electron microscope investigation of the silicification of four species of bacteria commonly found in the environment. The Gram positiveBacillus laterosporusand its spore produced a robust, durable crust upon silicification, whereas the Gram negativePseudomonas fluorescens, Ps. vesicularis, andPs. acidovoranspresented delicately preserved walls. The greater amount of peptidoglycan, containing abundant metal cation binding sites, in the cell wall of the Gram positive bacterium, probably accounts for the difference in the mode of fossilisation. The Gram positive bacteria are, therefore, probably most likely to be preserved in the terrestrial and extraterrestrial rock record.


Author(s):  
D. James Morré ◽  
Charles E. Bracker ◽  
William J. VanDerWoude

Calcium ions in the concentration range 5-100 mM inhibit auxin-induced cell elongation and wall extensibility of plant stems. Inhibition of wall extensibility requires that the tissue be living; growth inhibition cannot be explained on the basis of cross-linking of carboxyl groups of cell wall uronides by calcium ions. In this study, ultrastructural evidence was sought for an interaction of calcium ions with some component other than the wall at the cell surface of soybean (Glycine max (L.) Merr.) hypocotyls.


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