2010Xiandai yufang yixueRequires access

Development of method for Enterobacter sakazakii based by PCR in powdered milk.

Xiujuan Li, Baohong Xu, Huifang Tian

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Abstract

[Objective] To develop a PCR assay for detection of Enterobacter sakazakii in powdered milk.[Methods] Based on the zpx gene sequence of Enterobacter sakazakii to establish PCR assay,and to verify the specificity and sensitivity.Simulated samples and actual milk samples were tested.[Results] The sensitivity of PCR assay was 102cfu / ml in pure culture.Expected fragment(180bp) were produced from 6 strains of Enterobacter sakazakii after PCR amplification,but not from 31 strains of other bacteria.Enterobacter sakazakii were detected in simulated samples after pre-enrichment.The detection result of actual milk samples showed that there was a good consistency between the PCR assay and conventional method.[Conclusion] This PCR assay is accurate,sensitive,reliable,fast and easy.It should be used widely to detect Enterobacter sakazakii in powdered milk.

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What this paper is about

[Objective] To develop a PCR assay for detection of Enterobacter sakazakii in powdered milk.[Methods] Based on the zpx gene sequence of Enterobacter sakazakii to establish PCR assay,and to verify the specificity and sensitivity.Simulated samples and actual milk samples were tested.[Results] The sensitivity of PCR assay was 102cfu / ml in pure culture.Expected fragment(180bp) were produced from 6 strains of Enterobacter sakazakii after PCR amplification,but not from 31 strains of other bacteria.Enterobacter sakazakii were detected in simulated samples after pre-enrichment.The detection result of actual milk samples showed that there was a good consistency between the PCR assay and conventional method.[Conclusion] This PCR assay is accurate,sensitive,reliable,fast and easy.It should be used widely to detect Enterobacter sakazakii in powdered milk.

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Available abstract

[Objective] To develop a PCR assay for detection of Enterobacter sakazakii in powdered milk.[Methods] Based on the zpx gene sequence of Enterobacter sakazakii to establish PCR assay,and to verify the specificity and sensitivity.Simulated samples and actual milk samples were tested.[Results] The sensitivity of PCR assay was 102cfu / ml in pure culture.Expected fragment(180bp) were produced from 6 strains of Enterobacter sakazakii after PCR amplification,but not from 31 strains of other bacteria.Enterobacter sakazakii were detected in simulated samples after pre-enrichment.The detection result of actual milk samples showed that there was a good consistency between the PCR assay and conventional method.[Conclusion] This PCR assay is accurate,sensitive,reliable,fast and easy.It should be used widely to detect Enterobacter sakazakii in powdered milk.

Key concepts: Enterobacter, Microbiology, Gene sequence, Biology, Polymerase chain reaction, Food science, Bacteria, Gene

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Development of method for Enterobacter sakazakii based by PCR in powdered milk. — Research Paper | ScholarLens