Bacteria Detecting Instrument, Bacteria Detecting Method, and Bacteria Detecting Kit

Abstract

A micro array instrument is used in which an oligonucleotide based on a species- or genus-specific nucleotide sequence of subject bacteria is immobilized on a surface of a substrate. By confirming whether the oligonucleotide immobilized on the substrate has hybridized with a probe prepared from a test sample, bacteria contained in the test sample can be detected and identified easily, quickly, and accurately.

Description

[0001]This Nonprovisional application claims priority under U.S.C. § 119(a) on Patent Application No. 50523 / 2004 filed in Japan on Feb. 25, 2004, the entire contents of which are hereby incorporated by reference.TECHNICAL FIELD[0002]The present invention relates to bacteria detecting instruments, bacteria detecting methods, and bacteria detecting kits. Specifically, the invention relates to a bacteria detecting instrument in which bacteria-specific oligonucleotides are immobilized on a substrate surface, and to a highly accurate and user-friendly bacteria detecting method and bacteria detecting kit using such a bacteria detecting instrument.BACKGROUND ART[0003]Contamination of for example malt alcoholic beverages by harmful microorganisms is undesirable as it causes turbidity, off-flavor, or other adverse effects, which deteriorates product quality. Specifically, Lactobacillus, Pediococcus, and Pectinatus are some of the representative examples of harmful bacteria in beer. Among the...

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Benefits of technology

[0009]The present invention was made in view of the foregoing problems, and an object of the invention is to provide a bacteria detecting instrument in which an oligonucleotide for accurately detecting specific bacteria is immobilized on a substrate surface. The invention also provides a bacteria detecting method and bacteria detecting kit that, with use of the bacteria detecting instrument, allow for quick and accurate detection with simple procedures.

[0010]The inventors of the present invention diligently worked to solve the foregoing problems. In achieving the object, the inventors found a genus- or species-specific nucleotide sequence in the nucleotide sequences corresponding to the 16S ribosomal RNA genes of some of the representative spoilage bacteria in malt alcoholic beverages. With an instrument in which an oligonucleotide based on such a nucleotide sequence is immobilized on a substrate surface, quick and accurate detection and identification of bacteria was possible through hybridization with the nucleic acid derived from the test sample.

Problems solved by technology

Contamination of for example malt alcoholic beverages by harmful microorganisms is undesirable as it causes turbidity, off-flavor, or other adverse effects, which deteriorates product quality.

However, the method requires multiple rounds of PCR reactions, requiring a large number of primers for each different species of bacteria.

The method therefore requires complicated procedures, and is time consuming.

However, since there is a limit in the number of primers that can be used, it is difficult to obtain accurate results based on a trace amount of specimen.

However, it is not necessarily the case that such restriction enzymes are available for all species of bacteria to be tested.

Further, since the methods require the highly complicated procedure of excising the amplified product with several different kinds of restriction enzymes for electrophoresis, the methods are also problematic in terms of speed and convenience.

However, the methods employing hybridization also pose a problem in that crosshybridization with other species often occurs between closely related species having a high level of DNA homology.

As this is often the case, it is difficult to accurately identify bacterial species.

The methods having the problem of crosshybridization are particularly problematic when used for Lactobacillus bacteria, one of representative examples of beer spoilage bacteria, because many species of these bacteria are very closely related to one another.

As such is the case, the methods cannot be used for the detection and identification of harmful bacteria.

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