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嗜鱼肉杆菌LV17中肉杆菌素产生的转录分析与调控

Transcriptional analysis and regulation of carnobacteriocin production in Carnobacterium piscicola LV17.

作者信息

Saucier L, Paradkar A S, Frost L S, Jensen S E, Stiles M E

机构信息

Department of Biological Sciences, University of Alberta, Edmonton, Canada.

出版信息

Gene. 1997 Apr 1;188(2):271-7. doi: 10.1016/s0378-1119(96)00822-0.

Abstract

Bacteriocin production by Carnobacterium piscicola LV17 (carnobacteriocin, Cbn) depends on the level of inoculation when grown in liquid medium. With an inoculum of > or = 10(6) colony-forming units per ml (cfu/ml), bacteriocin production is observed during exponential growth, whereas with < or = 10(4) cfu/ml no bacteriocin is detected even when the culture has reached stationary phase. Using pure bacteriocins, it was demonstrated that bacteriocin production is autoregulated. To understand how bacteriocin production is regulated at the molecular level, cell-free supernatant from a bacteriocin-producing culture was added to fresh medium at 1% (v/v) together with a non-producing inoculum (10(4) cfu/ml), to induce bacteriocin production (induced culture). Northern analysis revealed major transcripts of 0.35, 1.5 and 1 kb for carnobacteriocins A, B2 and BM1, respectively, indicating that regulation of bacteriocin production by inoculum size occurs at the transcriptional level. Primer extension demonstrated that transcription initiated from the same promoters with the induced culture as with the positive control (culture inoculated at 10(7) cfu/ml). Quantitative phosphorimager analysis of the primer extension products indicated that cbnA transcript was more abundant than cbnB2 or cbnBM1.

摘要

嗜鱼肉杆菌LV17(肉杆菌素,Cbn)产生细菌素的情况取决于其在液体培养基中生长时的接种量。接种量≥10⁶ 菌落形成单位每毫升(cfu/ml)时,在指数生长期可观察到细菌素的产生,而接种量≤10⁴ cfu/ml时,即使培养物达到稳定期也检测不到细菌素。使用纯细菌素证明细菌素的产生是自动调节的。为了了解细菌素产生在分子水平上是如何调节的,将来自产生细菌素培养物的无细胞上清液以1%(v/v)的比例加入新鲜培养基中,并加入非产生菌接种物(10⁴ cfu/ml),以诱导细菌素的产生(诱导培养物)。Northern分析分别揭示了肉杆菌素A、B2和BM1的主要转录本大小为0.35、1.5和1 kb,这表明接种量对细菌素产生的调节发生在转录水平。引物延伸表明,诱导培养物与阳性对照(接种量为10⁷ cfu/ml的培养物)从相同的启动子开始转录。对引物延伸产物的定量磷光成像分析表明,cbnA转录本比cbnB2或cbnBM1更丰富。

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