دورية أكاديمية

Intraperiplasmic growth of Bdellovibrio bacteriovorus 109J: N-deacetylation of Escherichia coli peptidoglycan amino sugars.

التفاصيل البيبلوغرافية
العنوان: Intraperiplasmic growth of Bdellovibrio bacteriovorus 109J: N-deacetylation of Escherichia coli peptidoglycan amino sugars.
المؤلفون: Thomashow MF, Rittenberg SC
المصدر: Journal of bacteriology [J Bacteriol] 1978 Sep; Vol. 135 (3), pp. 1008-14.
نوع المنشور: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
اللغة: English
بيانات الدورية: Publisher: American Society for Microbiology Country of Publication: United States NLM ID: 2985120R Publication Model: Print Cited Medium: Print ISSN: 0021-9193 (Print) Linking ISSN: 00219193 NLM ISO Abbreviation: J Bacteriol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Washington, DC : American Society for Microbiology
مواضيع طبية MeSH: Escherichia coli*, Amidohydrolases/*metabolism , Amino Sugars/*metabolism , Bdellovibrio/*enzymology , Peptidoglycan/*metabolism, Bdellovibrio/growth & development ; Cytoplasm/microbiology ; Muramidase/pharmacology
مستخلص: During intraperiplasmic growth of Bdellovibrio bacteriovorus on Escherichia coli, the substrate cell peptidoglycan is extensively modified as it is converted to bdelloplast peptidoglycan. The initially lysozyme-sensitive peptidoglycan of E. coli was rapidly converted to a lysozyme-resistant form. The conversion was due to the N-deacetylation of a large portion of the peptidoglycan amino sugars. Chemically acetylating the isolated peptidoglycan restored its sensitivity to lysozyme digestion. However, approximately half of the products of lysozyme digestion exhibited hydrophobic interactions that were shown not to be due to the presence of protein. This suggests that a molecule capable of hydrophobic interactions, other than protein, becomes linked to the bdelloplast peptidoglycan. The data also suggest that much of the Braun lipoprotein is removed from the E. coli peptidoglycan early during bdellovibrio development.
References: J Gen Microbiol. 1960 Feb;22:158-66. (PMID: 13843470)
J Biol Chem. 1964 Sep;239:2981-5. (PMID: 14217885)
J Exp Med. 1961 Jul 1;114:127-40. (PMID: 13754097)
Biochim Biophys Acta. 1961 Jan 1;46:68-80. (PMID: 13738039)
Nature. 1958 Jun 28;181(4626):1783-4. (PMID: 13566139)
J Biol Chem. 1951 Nov;193(1):265-75. (PMID: 14907713)
Science. 1951 Mar 30;113(2935):354-5. (PMID: 14817299)
J Bacteriol. 1978 Sep;135(3):998-1007. (PMID: 357428)
J Bacteriol. 1978 Sep;135(3):1015-23. (PMID: 357411)
Biochemistry. 1970 Dec 22;9(26):5041-9. (PMID: 4249403)
Science. 1967 Apr 14;156(3772):213-21. (PMID: 4960294)
Biochem Biophys Res Commun. 1971 Nov 5;45(3):751-8. (PMID: 4256847)
J Bacteriol. 1974 May;118(2):663-80. (PMID: 4208138)
Ann N Y Acad Sci. 1974 May 10;235(0):66-82. (PMID: 4605152)
J Biol Chem. 1972 Oct 10;247(19):6312-22. (PMID: 4631319)
J Bacteriol. 1973 Feb;113(2):592-8. (PMID: 4632317)
J Biol Chem. 1973 Oct 25;248(20):7247-52. (PMID: 4582731)
J Bacteriol. 1968 Oct;96(4):1366-81. (PMID: 4879563)
J Bacteriol. 1966 May;91(5):2006-17. (PMID: 5327913)
المشرفين على المادة: 0 (Amino Sugars)
0 (Peptidoglycan)
EC 3.2.1.17 (Muramidase)
EC 3.5.- (Amidohydrolases)
تواريخ الأحداث: Date Created: 19780901 Date Completed: 19781129 Latest Revision: 20210526
رمز التحديث: 20240627
مُعرف محوري في PubMed: PMC222477
DOI: 10.1128/jb.135.3.1008-1014.1978
PMID: 357410
قاعدة البيانات: MEDLINE
الوصف
تدمد:0021-9193
DOI:10.1128/jb.135.3.1008-1014.1978