Dissociation of chitosomes by digitonin into 16 S subunits with chitin synthetase activity
Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy- D-glucose : chitin 4-β-acetamidodeoxy- D-glucosyltransferase, EC 2.4.1.1...
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Published in | Biochimica et biophysica acta Vol. 629; no. 2; pp. 201 - 216 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
07.05.1980
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Online Access | Get full text |
ISSN | 0304-4165 0006-3002 1872-8006 1878-2434 |
DOI | 10.1016/0304-4165(80)90094-X |
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Abstract | Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus
Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy-
D-glucose : chitin 4-β-acetamidodeoxy-
D-glucosyltransferase, EC 2.4.1.16) activity; at higher concentrations, it inhibits it. Digitonin also causes disintegration of the chitosome and the release of a homogeneous population of chitosome subunits with chitin synthetase activity. These chitosome subunits have a sedimentation coefficient of 16 S, compared to 105 S for whole chitosomes, as determined by centrifugation in sucrose density gradients, and measure 7–12 nm in diameter. After dissociation, chitin synthetase remains in a zymogenic state, and requires treatment with a protease for activation. No change in sedimentation coefficient of chitosome subunits was observed after proteolytic activation. The product synthesized by the chitosome subunits was characterized by X-ray diffractometry as α-chitin and was by this criterion indistinguishable from chitin made by preparations of undissociated chitosomes. However, in the electron microscope, the chitin microfibrils made from chitosome subunits were, in general, much shorter than those produced by undissociated chitosomes and often exhibited a needle-like appearance. |
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AbstractList | Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy-D-glucose: chitin 4-beta acetamidodeoxy-D-glucosyltransferase, EC 2.4.1.16) activity; at higher concentrations, it inhibits it. Digitonin also causes disintegration of the chitosome and the release of a homogeneous population of chitosome subunits with chitin synthetase activity. These chitosome subunits have a sedimentation coefficient of 16 S, compared to 105 S for whole chitosomes, as determined by centrifugation in sucrose density gradients, and measure 7--12 nm in diameter. After dissociation, chitin synthetase remains in a zymogenic state, and requires treatment with a protease for activation. No change in sedimentation coefficient of chitosome subunits was observed after proteolytic activation. The product synthesized by the chitosome subunits was characterized by X-ray diffractometry ad alpha-chitin and was by the criterion indistinfuishable from chitin made by preparations of undissociated chitosomes. However, in the electron microscope, the chitin microfibrils made from chitosome subunits were, in general, much shorter than those produced by undissociated chitosomes and often exhibited a needle-like appearance. Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy-D-glucose: chitin 4-beta acetamidodeoxy-D-glucosyltransferase, EC 2.4.1.16) activity; at higher concentrations, it inhibits it. Digitonin also causes disintegration of the chitosome and the release of a homogeneous population of chitosome subunits with chitin synthetase activity. These chitosome subunits have a sedimentation coefficient of 16 S, compared to 105 S for whole chitosomes, as determined by centrifugation in sucrose density gradients, and measure 7--12 nm in diameter. After dissociation, chitin synthetase remains in a zymogenic state, and requires treatment with a protease for activation. No change in sedimentation coefficient of chitosome subunits was observed after proteolytic activation. The product synthesized by the chitosome subunits was characterized by X-ray diffractometry ad alpha-chitin and was by the criterion indistinfuishable from chitin made by preparations of undissociated chitosomes. However, in the electron microscope, the chitin microfibrils made from chitosome subunits were, in general, much shorter than those produced by undissociated chitosomes and often exhibited a needle-like appearance.Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy-D-glucose: chitin 4-beta acetamidodeoxy-D-glucosyltransferase, EC 2.4.1.16) activity; at higher concentrations, it inhibits it. Digitonin also causes disintegration of the chitosome and the release of a homogeneous population of chitosome subunits with chitin synthetase activity. These chitosome subunits have a sedimentation coefficient of 16 S, compared to 105 S for whole chitosomes, as determined by centrifugation in sucrose density gradients, and measure 7--12 nm in diameter. After dissociation, chitin synthetase remains in a zymogenic state, and requires treatment with a protease for activation. No change in sedimentation coefficient of chitosome subunits was observed after proteolytic activation. The product synthesized by the chitosome subunits was characterized by X-ray diffractometry ad alpha-chitin and was by the criterion indistinfuishable from chitin made by preparations of undissociated chitosomes. However, in the electron microscope, the chitin microfibrils made from chitosome subunits were, in general, much shorter than those produced by undissociated chitosomes and often exhibited a needle-like appearance. Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low concentrations, it stimulates chitin synthetase (UDP-2-acetamido-2-deoxy- D-glucose : chitin 4-β-acetamidodeoxy- D-glucosyltransferase, EC 2.4.1.16) activity; at higher concentrations, it inhibits it. Digitonin also causes disintegration of the chitosome and the release of a homogeneous population of chitosome subunits with chitin synthetase activity. These chitosome subunits have a sedimentation coefficient of 16 S, compared to 105 S for whole chitosomes, as determined by centrifugation in sucrose density gradients, and measure 7–12 nm in diameter. After dissociation, chitin synthetase remains in a zymogenic state, and requires treatment with a protease for activation. No change in sedimentation coefficient of chitosome subunits was observed after proteolytic activation. The product synthesized by the chitosome subunits was characterized by X-ray diffractometry as α-chitin and was by this criterion indistinguishable from chitin made by preparations of undissociated chitosomes. However, in the electron microscope, the chitin microfibrils made from chitosome subunits were, in general, much shorter than those produced by undissociated chitosomes and often exhibited a needle-like appearance. |
Author | Bartnicki-Garcia, S. Ruiz-Herrera, J. Bracker, C.E. |
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Keywords | Chitin synthetase Chitosome dissociation Digitonin |
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References | Ruiz-Herrera, Lopez-Romero, Bartnicki-Garcia (BIB2) 1977; 252 Brakke, Van Pelt (BIB17) 1970; 38 Stafford, Brummond (BIB8) 1970; 9 Tsai, Hassid (BIB9) 1971; 47 Ruiz-Herrera, Sing, Van Der Woude, Bartnicki-Garcia (BIB4) 1975; 72 Bartnicki-Garcia, Ruiz-Herrera, Bracker (BIB5) 1979 Bracker, Ruiz-Herrera, Bartnicki-Garcia (BIB1) 1976; 73 De Rousset-Hall, Gooday (BIB12) 1975; 89 Schlamowitz, Peterson (BIB19) 1959; 234 Duran, Cabib (BIB14) 1978; 253 Umezawa, Aoyagi, Morishima, Matsuzaki, Hamada, Takeuchi (BIB20) 1970; 23 Feingold, Neufeld, Hassid (BIB6) 1958; 233 McMurrough, Flores-Carreon, Bartnicki-Garcia (BIB18) 1971; 246 Bartnicki-Garcia, Bracker, Reyes, Ruiz-Herrera (BIB3) 1978; 2 Chambers, Elbein (BIB10) 1970; 138 Hernandez, Cerbon, Ruiz-Herrera (BIB24) 1979 Gooday, De Rousset-Hall (BIB11) 1975; 89 Bartnicki-Garcia, Nickerson (BIB16) 1962; 84 Ruiz-Herrera, Bartnicki-Garcia (BIB23) 1974; 186 Lopez-Romero, Ruiz-Herrera, Bartnicki-Garcia (BIB21) 1978; 525 Liu, Hassid (BIB7) 1970; 245 Keller, Cabib (BIB22) 1971; 246 Bartnicki-Garcia, Bracker, Ruiz-Herrera (BIB25) 1977 Ruiz-Herrera, Bartnicki-Garcia, Bracker (BIB15) 1976 Duran, Bowers, Cabid (BIB13) 1976; 35 |
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Snippet | Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus
Mucor rouxii). At low... Digitonin exerts profound effects on chitosomes (microvesicular structures with chitin synthetase activity isolated from the fungus Mucor rouxii). At low... |
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SubjectTerms | Centrifugation, Density Gradient Chitin - biosynthesis Chitin Synthase - isolation & purification Chitin Synthase - metabolism Chitin synthetase Chitosome dissociation Digitonin Digitonin - pharmacology fungi Glucosyltransferases - metabolism Microscopy, Electron Molecular Conformation - drug effects Mucor - metabolism Mucor - ultrastructure |
Title | Dissociation of chitosomes by digitonin into 16 S subunits with chitin synthetase activity |
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