Rasch Maria, Andersen Jens Bo, Nielsen Kristian Fog, Flodgaard Lars Ravn, Christensen Henrik, Givskov Michael, Gram Lone
Danish Institute for Fisheries Research, Department of Seafood Research, Søltofts Plads, c/o Technical University of Denmark Bldg. 221, DK-2800 Kgs. Lyngby, Denmark.
Appl Environ Microbiol. 2005 Jun;71(6):3321-30. doi: 10.1128/AEM.71.6.3321-3330.2005.
Bacterial communication signals, acylated homoserine lactones (AHLs), were extracted from samples of commercial bean sprouts undergoing soft-rot spoilage. Bean sprouts produced in the laboratory did not undergo soft-rot spoilage and did not contain AHLs or AHL-producing bacteria, although the bacterial population reached levels similar to those in the commercial sprouts, 10(8) to 10(9) CFU/g. AHL-producing bacteria (Enterobacteriaceae and pseudomonads) were isolated from commercial sprouts, and strains that were both proteolytic and pectinolytic were capable of causing soft-rot spoilage in bean sprouts. Thin-layer chromatography and liquid chromatography-high-resolution mass spectrometry revealed the presence of N-3-oxo-hexanoyl-l-homoserine lactone in spoiled bean sprouts and in extracts from pure cultures of bacteria. During normal spoilage, the pH of the sprouts increased due to proteolytic activity, and the higher pH probably facilitated the activity of pectate lyase. The AHL synthetase gene (I gene) from a spoilage Pectobacterium was cloned, sequenced, and inactivated in the parent strain. The predicted amino acid sequence showed 97% homology to HslI and CarI in Erwinia carotovora. Spoilage of laboratory bean sprouts inoculated with the AHL-negative mutant was delayed compared to sprouts inoculated with the wild type, and the AHL-negative mutant did not cause the pH to rise. Compared to the wild-type strain, the AHL-negative mutant had significantly reduced protease and pectinase activities and was negative in an iron chelation (siderophore) assay. This is the first study demonstrating AHL regulation of iron chelation in Enterobacteriaceae. The present study clearly demonstrates that the bacterial spoilage of some food products is influenced by quorum-sensing-regulated phenotypes, and understanding these processes may be useful in the development of novel food preservation additives that specifically block the quorum-sensing systems.
从发生软腐变质的市售豆芽样品中提取了细菌通讯信号——酰化高丝氨酸内酯(AHLs)。实验室培育的豆芽未发生软腐变质,也不含AHLs或产AHLs的细菌,尽管其细菌数量达到了与市售豆芽相似的水平,即10⁸至10⁹CFU/g。从市售豆芽中分离出产AHLs的细菌(肠杆菌科细菌和假单胞菌),同时具有蛋白水解和果胶水解能力的菌株能够在豆芽中引起软腐变质。薄层色谱法和液相色谱 - 高分辨率质谱分析表明,在变质豆芽和细菌纯培养物提取物中存在N - 3 - 氧代 - 己酰基 - L - 高丝氨酸内酯。在正常变质过程中,由于蛋白水解活性,豆芽的pH值升高,而较高的pH值可能促进了果胶酸裂解酶的活性。从一株引起变质的果胶杆菌中克隆、测序了AHL合成酶基因(I基因),并使其在亲本菌株中失活。预测的氨基酸序列与胡萝卜软腐欧文氏菌中的HslI和CarI具有97%的同源性。与接种野生型的豆芽相比,接种AHL阴性突变体的实验室豆芽的变质延迟,且AHL阴性突变体不会导致pH值升高。与野生型菌株相比,AHL阴性突变体的蛋白酶和果胶酶活性显著降低,并且在铁螯合(铁载体)试验中呈阴性。这是首次证明肠杆菌科中铁螯合受AHL调控的研究。本研究清楚地表明,某些食品的细菌变质受群体感应调控的表型影响,了解这些过程可能有助于开发特异性阻断群体感应系统的新型食品保鲜添加剂。