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Involvement of Bacterial Quorum-Sensing Signals in Spoilage of Bean Sprouts

机译:细菌群体感应信号参与豆芽腐败变质

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摘要

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, 108 to 109 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.
机译:从经历软腐变质的商品豆芽样品中提取细菌通讯信号,酰化高丝氨酸内酯(AHL)。实验室生产的豆芽未发生软腐变质,并且不含AHL或产生AHL的细菌,尽管细菌数量达到了与商业豆芽相似的水平,即10 8 至10 < sup> 9 CFU / g。从商业芽苗中分离出产生AHL的细菌(肠杆菌科和假单胞菌),蛋白水解和果胶分解的菌株都能够在豆芽中引起软腐腐败。薄层色谱和液相色谱-高分辨率质谱分析显示,在变质的豆芽和纯细菌培养物中,存在N-3-氧代己酰基-1-高丝氨酸内酯。在正常变质过程中,由于蛋白水解活性,新芽的pH值升高,而较高的pH值可能促进了果胶酸裂合酶的活性。从腐败菌中分离出AHL合成酶基因(I基因),测序并在亲本菌株中失活。预测的氨基酸序列与胡萝卜欧文氏菌中的HslI和CarI具有97%的同源性。与野生型接种的豆芽相比,接种AHL阴性的豆芽实验室的变质被延迟了,并且AHL阴性的突变株没有引起pH的升高。与野生型菌株相比,AHL阴性突变体具有明显降低的蛋白酶和果胶酶活性,在铁螯合(铁载体)测定中呈阴性。这是第一个证明AHL调节肠杆菌科中铁螯合的研究。本研究清楚地表明,某些食品的细菌变质受到群体感应调节的表型的影响,并且了解这些过程可能有助于开发专门阻止群体感应系统的新型食品防腐添加剂。

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