Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Tytuł pozycji:

[Function of luxS gene in sulfurmetabolism of Streptococcus mutans].

Tytuł:
[Function of luxS gene in sulfurmetabolism of Streptococcus mutans].
Autorzy:
Yu DN; Department of Stomatology, The Second Hospital of Tianjin Medical University, Tianjin 300211, China. />Ren ZM
Han YZ
Zhang WJ
Źródło:
Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology [Zhonghua Kou Qiang Yi Xue Za Zhi] 2011 Apr; Vol. 46 (4), pp. 210-3.
Typ publikacji:
English Abstract; Journal Article; Research Support, Non-U.S. Gov't
Język:
Chinese
Imprint Name(s):
Publication: Beijing : Chinese Medical Association
Original Publication: Beijing : Zhonghua yi xue hui, 1987-
MeSH Terms:
Quorum Sensing*
Bacterial Proteins/*metabolism
Biofilms/*growth & development
Carbon-Sulfur Lyases/*metabolism
Streptococcus mutans/*growth & development
Bacterial Proteins/genetics ; Carbon-Sulfur Lyases/genetics ; Culture Media ; Culture Techniques ; Cysteine/metabolism ; Gene Expression Regulation, Bacterial ; Methionine/metabolism ; Microscopy, Confocal ; S-Adenosylhomocysteine/metabolism ; S-Adenosylmethionine/metabolism ; Streptococcus mutans/genetics ; Streptococcus mutans/metabolism ; Sulfur/metabolism
Substance Nomenclature:
0 (Bacterial Proteins)
0 (Culture Media)
70FD1KFU70 (Sulfur)
7LP2MPO46S (S-Adenosylmethionine)
979-92-0 (S-Adenosylhomocysteine)
AE28F7PNPL (Methionine)
EC 4.4.- (Carbon-Sulfur Lyases)
EC 4.4.1.21 (LuxS protein, Bacteria)
K848JZ4886 (Cysteine)
Entry Date(s):
Date Created: 20110527 Date Completed: 20140911 Latest Revision: 20110526
Update Code:
20240104
PMID:
21612708
Czasopismo naukowe
Objective: To investigate the function of luxS in sulfurmetabolism of Streptococcus mutans (Sm).
Methods: The growth with absorbency (A) of the standards and mutant strains was measured and analyzed in the sulfur-limited defined medium at different periods. The laser scanning confocal microscopy (LSCM) was used to observe and compare the biofilm thickness of the two kinds of strains at different culture conditions.
Results: The significant increases in the thickness of mutant strain biofilm and its growth were observed after the addition of cysteine, but did not reach the standards strain levels (P < 0.05). The growth and the biofilm thickness of the mutant strains were (1.301 ± 0.009) and (45.009 ± 0.429) µm. When methionine and S-adenosylhomocysteine of certain concentrations were respectively added, the biofilm thickness and the growth of mutant strain were raised but did not reach the level of the standards strain at 24 h (P < 0.05), but at 48 h they did. When the methionine was added in the mutant strains for 24 h, the biofilm thickness and the growth of mutant strain were (0.448 ± 0.028) and (37.068 ± 2.392) µm, as for the adding of S-adenosylhomocysteine were (0.460 ± 0.005) and (27.343 ± 1.107) µm. When adding the supernatant fluid of standard strains, the biofilm thickness and the growth levels of mutant strain were much higher than those of the standards strain. The biofilm thickness and growth of both kinds of strains decreased after the addition of S-adenosylmethionine.
Conclusions: luxS gene plays not only a role in quorum sensing but also a role in sulfurmetabolism.

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies