Suppr超能文献

荧光假单胞菌分离株中与食品腐败相关的酶。

Enzymes from isolates of Pseudomonas fluorescens involved in food spoilage.

作者信息

Rajmohan S, Dodd C E R, Waites W M

机构信息

Division of Food Sciences, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire, UK.

出版信息

J Appl Microbiol. 2002;93(2):205-13. doi: 10.1046/j.1365-2672.2002.01674.x.

Abstract

AIMS

Psychrotrophic Gram-negative bacteria, such as Pseudomonas species, pose a significant spoilage problem in refrigerated meat and dairy products due to secretion of hydrolytic enzymes, especially lipases and proteases. This study characterized the enzymes produced by strains of Pseudomonas fluorescens isolated from pasteurized milk.

METHODS AND RESULTS

Thirty-seven isolates of Ps. fluorescens from skimmed, semiskimmed and whole milk were all shown to be proteolytic and lipolytic on casein and tributyrin agar, respectively. The highest level of protease production by one isolate, SMD 31, from skimmed milk was in minimal salts medium containing 1 mmol x l(-1) calcium chloride at 20 degrees C. The proteases belonged to the class of metallo-proteases, as there was no residual activity with 10 mmol x l(-1) EDTA. They were heat stable and retained activity even after treatment at 121 degrees C for 20 min. One protease of 45-48 kDa was detected in unconcentrated supernatant fluid samples but, in three isolates from different milk sources, five proteases with molecular masses between 28 and 48 kDa were detected on a 12% zymogram casein gel following ultrafiltration. Attempts to purify the lipases proved unsuccessful.

CONCLUSIONS

The characteristics of the major protease of 45-48 kDa correspond to those of proteases described for other Pseudomonas species isolated from a range of environments. However, the smaller proteases have not been described previously.

SIGNIFICANCE AND IMPACT OF THE STUDY

In the absence of ultrafiltration the presence of the minor protease species may be missed and they may act as contaminants of the major protease in unpurified or semipurified samples.

摘要

目的

嗜冷革兰氏阴性菌,如假单胞菌属,由于其水解酶特别是脂肪酶和蛋白酶的分泌,在冷藏肉类和乳制品中造成严重的腐败问题。本研究对从巴氏杀菌乳中分离出的荧光假单胞菌菌株所产生的酶进行了特性鉴定。

方法与结果

从脱脂乳、半脱脂乳和全脂乳中分离出的37株荧光假单胞菌在酪蛋白和三丁酸甘油酯琼脂平板上分别表现出蛋白水解和脂肪水解活性。从脱脂乳中分离出的一株菌株SMD 31在含有1 mmol/L氯化钙的基本盐培养基中于20℃时蛋白酶产量最高。这些蛋白酶属于金属蛋白酶类,因为在加入10 mmol/L乙二胺四乙酸(EDTA)后没有残留活性。它们具有热稳定性,即使在121℃处理20分钟后仍保留活性。在未浓缩的上清液样品中检测到一种45 - 48 kDa的蛋白酶,但在来自不同奶源的三株菌株中,超滤后在12%的酪蛋白酶谱凝胶上检测到5种分子量在28至48 kDa之间的蛋白酶。纯化脂肪酶的尝试未成功。

结论

45 - 48 kDa主要蛋白酶的特性与从一系列环境中分离出的其他假单胞菌属所描述的蛋白酶特性相符。然而,较小的蛋白酶此前尚未见报道。

研究的意义与影响

在没有超滤的情况下,可能会遗漏次要蛋白酶种类的存在,并且它们可能在未纯化或半纯化样品中作为主要蛋白酶的污染物起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验