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Yun Deng

Researcher at Center for Food Safety

Publications -  5
Citations -  248

Yun Deng is an academic researcher from Center for Food Safety. The author has contributed to research in topics: Acetic acid & Tryptic soy broth. The author has an hindex of 4, co-authored 4 publications receiving 247 citations.

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Journal ArticleDOI

Behavior of acid-adapted and unadapted Escherichia coli O157:H7 when exposed to reduced pH achieved with various organic acids.

TL;DR: It is shown that organic acids differ in their inhibitory or lethal activity against acid- Adapted and unadapted E. coli O157:H7 cells, and acid-adapted cells are more tolerant than un Adapted cells when subsequently exposed to reduced pH caused by these acids.
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Tolerance of acid-adapted and non-adapted Escherichia coli O157:H7 cells to reduced pH as affected by type of acidulant

TL;DR: There was essentially no difference in growth characteristics of the two types of cells in TSB acidified at the same pH with a given acid, and on plates not showing visible colonies, acid‐ Adapted cells retained higher viability than unadapted cells when plated on acidified TSA.
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Influence of temperature and pH on survival of Escherichia coli O157:H7 in dry foods and growth in reconstituted infant rice cereal

TL;DR: Survival appeared to be enhanced in foods with highest pH, and acid- Adapted cells retained higher viability than unadapted cells in only two of the nine test foods, particularly at refrigeration temperature.
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Survival of Escherichia coli O157:H7 in dried beef powder as affected by water activity, sodium chloride content and temperature.

TL;DR: In this paper, a study was carried out to determine the rate of inactivation of Escherichia coli O157:H7 in beef powder as affected by aw(0·34±0·06± 0·01), sodium chloride content (0·5, 3·0 and 20%) and temperature (5 and 25° C) over an 8-week storage time.
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Association analysis of rice resistance genes and blast fungal avirulence genes for effective breeding resistance cultivars

TL;DR: In this paper , the changes of rice blast-resistance (R) genes over time and their ultimate impact on pathogen AVR genes were analyzed by PCR using gene-specific markers of the nine R genes and six primer pairs targeting the coding sequence or promoter of AVR, respectively.