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合成培养基和豌豆粉中微生物对植酸盐的降解

Phytate degradation by micro-organisms in synthetic media and pea flour.

作者信息

Fredrikson M, Andlid T, Haikara A, Sandberg A-S

机构信息

Department of Food Science, Chalmers University of Technology, Göteborg, Sweden.

出版信息

J Appl Microbiol. 2002;93(2):197-204. doi: 10.1046/j.1365-2672.2002.01676.x.

Abstract

AIMS

To screen micro-organisms for the ability to produce phytase enzyme(s) and to use promising strains for the fermentation of pea flour.

METHODS AND RESULTS

Two methods using the indirect estimation of phytate degradation were evaluated and both shown to be inadequate. A third method, measuring the inositol phosphate (IP3-IP6) content directly during fermentation, was used instead of the indirect estimations of phytate degradation. In synthetic media, some strains required customized conditions, with no accessible phosphorus sources other than phytate, to express phytase activity. The repression of phytase synthesis by inorganic phosphorus was not detected during fermentation with pea flour as substrate and seemed to be less significant with a higher composition complexity of the substrate. None of the tested lactic acid bacteria strains showed phytase activity.

CONCLUSIONS

The methodology for the phytase screening procedure was shown to be critical. Some of the screening methods and media used in previous publications were found to be inadequate.

SIGNIFICANCE AND IMPACT OF THE STUDY

This paper highlights the pitfalls and difficulties in the evaluation of phytase production by micro-organisms. The study is of great importance for future studies in this area.

摘要

目的

筛选具有产生植酸酶能力的微生物,并使用有前景的菌株进行豌豆粉发酵。

方法与结果

评估了两种使用间接估计植酸盐降解的方法,结果表明这两种方法均不适用。取而代之的是采用第三种方法,即在发酵过程中直接测量肌醇磷酸(IP3 - IP6)含量,而不是间接估计植酸盐降解。在合成培养基中,一些菌株需要定制条件,除了植酸盐外没有其他可利用的磷源,才能表达植酸酶活性。以豌豆粉为底物发酵时,未检测到无机磷对植酸酶合成的抑制作用,而且随着底物组成复杂性的增加,这种抑制作用似乎不太明显。所测试的乳酸菌菌株均未显示出植酸酶活性。

结论

结果表明植酸酶筛选程序的方法至关重要。发现先前出版物中使用的一些筛选方法和培养基并不适用。

研究的意义与影响

本文强调了评估微生物产生植酸酶时存在的陷阱和困难。该研究对该领域未来的研究具有重要意义。

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