東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Transcription analysis of the nisin ...

Li, Haiping.

FindBook

Google Book

Amazon

博客來

Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454./
作者:	Li, Haiping.
面頁冊數:	153 p.
附註:	Source: Dissertation Abstracts International, Volume: 66-04, Section: B, page: 1881.
Contained By:	Dissertation Abstracts International66-04B.
標題:	Biology, Microbiology. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3172819
ISBN:	0542099357

Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454.
Li, Haiping.

Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454. - 153 p.

Source: Dissertation Abstracts International, Volume: 66-04, Section: B, page: 1881.

Thesis (Ph.D.)--University of Minnesota, 2005.

The biosynthesis of the antimicrobial peptide nisin by Lactococcus lactis ATCC 11454 is subject to autoregulation. Transcriptions of nisABTCIP, where nisI encodes an immunity protein, and nisFEG, which encode an ABC transporter, are tightly induced by external nisin via the two-component system NisRK. One objective of this thesis is to study how sufficient immunity (NisI) can be expressed when the cell first encounters external nisin. In this study, Northern-blot and RT-PCR showed that nisI mRNA was present independent of nisA mRNA. Further mRNA stability study demonstrated that nisI mRNA had a much shorter half-life compared to nisA mRNA, suggesting that an internal promoter within nisABTCIP operon caused the independent nisI transcription that further provided cell immunity prior to the initiation of nisin auto-induction. The promoter was confirmed when the adjacent upstream region of nisI was fused to a probe vector, exhibiting constitutive promoter activity. The transcription start site (TSS) of the promoter was further mapped at 123 bp upstream of the ATG codon. Ordered 5' deletions revealed that transcription activation depended on sequences located up to -234 bp from the TSS.

ISBN: 0542099357Subjects--Topical Terms:

1017734
Biology, Microbiology.

Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454.
LDR:03258nmm 2200289 4500 001 1815484
005 20060710102004.5
008 130610s2005 eng d
020 $a 0542099357
035 $a (UnM)AAI3172819
035 $a AAI3172819
040 $a UnM $c UnM
100 1 $a Li, Haiping. $3 1904905
245 1 0 $a Transcription analysis of the nisin gene cluster in Lactococcus lactis ATCC 11454.
300 $a 153 p.
500 $a Source: Dissertation Abstracts International, Volume: 66-04, Section: B, page: 1881.
500 $a Adviser: Daniel Joseph O'Sullivan.
502 $a Thesis (Ph.D.)--University of Minnesota, 2005.
520 $a The biosynthesis of the antimicrobial peptide nisin by Lactococcus lactis ATCC 11454 is subject to autoregulation. Transcriptions of nisABTCIP, where nisI encodes an immunity protein, and nisFEG, which encode an ABC transporter, are tightly induced by external nisin via the two-component system NisRK. One objective of this thesis is to study how sufficient immunity (NisI) can be expressed when the cell first encounters external nisin. In this study, Northern-blot and RT-PCR showed that nisI mRNA was present independent of nisA mRNA. Further mRNA stability study demonstrated that nisI mRNA had a much shorter half-life compared to nisA mRNA, suggesting that an internal promoter within nisABTCIP operon caused the independent nisI transcription that further provided cell immunity prior to the initiation of nisin auto-induction. The promoter was confirmed when the adjacent upstream region of nisI was fused to a probe vector, exhibiting constitutive promoter activity. The transcription start site (TSS) of the promoter was further mapped at 123 bp upstream of the ATG codon. Ordered 5' deletions revealed that transcription activation depended on sequences located up to -234 bp from the TSS.
520 $a Another objective of this thesis is to study the repressive mechanism of high growth temperature on nisin production. RT-PCR and Western-hybridization showed that nisR was transcribed and translated while nisA was repressed, eliminating the possibility that lack of NisRK caused the loss of nisA transcription. Gel shift experiments demonstrated no nisA-binding proteins present in cell extracts following a growth at 40°C, indicating lack of activated NisR at high growth temperature. Heparin column purification of nisA binding proteins and isolation of total phosphorylated proteins substantiated this finding as neither other repressor(s) nor phosphorylated NisR could be detected at 40°C. Therefore, it could be concluded that the absence of nisA transcription at 40°C was due to a lack of phosphorylated NisR which is needed to activate transcription of nisA. Further analysis of the NisK kinase activity at 40°C showed a significant repression, elucidating the reason of lacking phosphorylated NisR at 40°C. The relationship between reduced NisK kinase and cell morphology change was also discussed.
590 $a School code: 0130.
650 4 $a Biology, Microbiology. $3 1017734
650 4 $a Agriculture, Food Science and Technology. $3 1017813
690 $a 0410
690 $a 0359
710 2 0 $a University of Minnesota. $3 676231
773 0 $t Dissertation Abstracts International $g 66-04B.
790 1 0 $a O'Sullivan, Daniel Joseph, $e advisor
790 $a 0130
791 $a Ph.D.
792 $a 2005
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3172819