Ömer Eren
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Ömer Eren has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Aydın Erge
Bolu Abant İzzet Baysal Üniversitesi
2 shared publications - Büşra Zeynep Güler
Bolu Abant İzzet Baysal University, Faculty of Agriculture, Poultry Science Department, Gölköy Campus, Bolu, Turkey
1 shared publication - Kubra Eryasar-Orer
Department of Food Engineering, Faculty of Engineering, Bolu Abant Izzet Baysal University, Bolu, Turkey
1 shared publication - Nursel Söylemez Milli
Scientific, Industrial and Technological Application and Research Centre, Bolu Abant İzzet Baysal University, 14030 Bolu, Türkiye
1 shared publication - Seda Karasu-Yalcin
Faculty of Engineering, Department of Food Engineering, Bolu Abant Izzet Baysal University, Bolu, Türkiye
1 shared publication
Latest Publications
- 3 November 2023
- Published by Elsevier in Food Chemistry
- Vol. 438, 137923
Optimization and characterization of biodegradable films from chicken gelatin crosslinked with oxidized phenolic compounds
- 3 November 2023
- Published by Elsevier in Food Chemistry
- Vol. 438, 137923
Optimization and characterization of biodegradable films from chicken gelatin crosslinked with oxidized phenolic compounds
- 1 July 2021
- Published by Elsevier in Food Chemistry
- Vol. 351, 129269
Chicken gelatin modification by caffeic acid: A response surface methodology investigation
- 1 July 2021
- Published by Elsevier in Food Chemistry
- Vol. 351, 129269
Chicken gelatin modification by caffeic acid: A response surface methodology investigation
- 23 October 2020
- Published by Springer Nature in Journal of Food Science and Technology
- Vol. 58 (11) , 4102-4109
Reducing time in detection of Listeria monocytogenes from food by MALDI-TOF mass spectrometry
In this study, direct detection of L. monocytogenes from liquid culture and enrichment broths containing foods was investigated by using MALDI-TOF MS. For determining the sole effect of food constituents on detection and accuracy of identification in enrichment broths, sterile foods were used before the experiments with food. L. monocytogenes could be detected in BHI broth after 24 h of incubation. Detection period was determined as 18 h for 3 × 101 cfu/mL initial bacterial count in BHI broth containing sterile food. The period extended in ONE broth containing sterile garnish, which was 24 and 30 h for 3 × 101 and 1 cfu/mL inoculum, respectively. It was found that identification times in UHT milk were longer than that of canned garnish. In the experiments performed with foods having a specific microbiota; White cheese, iceberg lettuce, parsley and watermelon were used. Although no reliable identification was obtained by using White cheese, iceberg lettuce and parsley, L. monocytogenes could be detected in 24 h in the enrichment broth containing watermelon. Detection was achieved during a single step enrichment in a reduced time of 24 h for even 1 cfu/mL initial inoculum.
- 23 October 2020
- Published by Springer Nature in Journal of Food Science and Technology
- Vol. 58 (11) , 4102-4109
Reducing time in detection of Listeria monocytogenes from food by MALDI-TOF mass spectrometry
In this study, direct detection of L. monocytogenes from liquid culture and enrichment broths containing foods was investigated by using MALDI-TOF MS. For determining the sole effect of food constituents on detection and accuracy of identification in enrichment broths, sterile foods were used before the experiments with food. L. monocytogenes could be detected in BHI broth after 24 h of incubation. Detection period was determined as 18 h for 3 × 101 cfu/mL initial bacterial count in BHI broth containing sterile food. The period extended in ONE broth containing sterile garnish, which was 24 and 30 h for 3 × 101 and 1 cfu/mL inoculum, respectively. It was found that identification times in UHT milk were longer than that of canned garnish. In the experiments performed with foods having a specific microbiota; White cheese, iceberg lettuce, parsley and watermelon were used. Although no reliable identification was obtained by using White cheese, iceberg lettuce and parsley, L. monocytogenes could be detected in 24 h in the enrichment broth containing watermelon. Detection was achieved during a single step enrichment in a reduced time of 24 h for even 1 cfu/mL initial inoculum.