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Large-Scale Production of Cronobacter sakazakii Bacteriophage Φ CS01 in Bioreactors via a Two-Stage Self-Cycling Process.
Lee, Jin-Sun; Kim, Gyeong-Hwuii; Kim, Jaegon; Lim, Tae-Hyun; Yoon, Yongwon; Yoon, Sung-Sik.
Affiliation
  • Lee JS; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
  • Kim GH; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
  • Kim J; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
  • Lim TH; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
  • Yoon Y; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
  • Yoon SS; Department of Biological Science and Technology, Yonsei University, Wonju 26493, Republic of Korea.
J Microbiol Biotechnol ; 31(10): 1430-1437, 2021 Oct 28.
Article in En | MEDLINE | ID: mdl-34489375
ABSTRACT
Cronobacter sakazakii is an opportunistic pathogenic bacterium found in powdered infant formula and is fatal to neonates. Antibiotic resistance has emerged owing to overuse of antibiotics. Therefore, demand for high-yield bacteriophages as an alternative to antibiotics has increased. Accordingly, we developed a modified mass-production method for bacteriophages by introducing a two-stage self-cycling (TSSC) process, which yielded high-concentration bacteriophage solutions by replenishing the nutritional medium at the beginning of each process, without additional challenge. pH of the culture medium was monitored in real-time during C. sakazakii growth and bacteriophage CS01 propagation, and the changes in various parameters were assessed. The pH of the culture medium dropped to 5.8 when the host bacteria reached the early log phase (OD540 = 0.3). After challenge, it decreased to 4.65 and then recovered to 4.94; therefore, we set the optimum pH to challenge the phage at 5.8 and that to harvest the phage at 4.94. We then compared phage production during the TSSC process in jar-type bioreactors and the batch culture process in shaker flasks. In the same volume of LB medium, the concentration of the phage titer solution obtained with the TSSC process was 24 times higher than that obtained with the batch culture process. Moreover, we stably obtained high concentrations of bacteriophage solutions for three cycles with the TSSC process. Overall, this modified TSSC process could simplify large-scale production of bacteriophage CS01 and reduce the unit cost of phage titer solution. These results could contribute to curing infants infected with antibiotic-resistant C. sakazakii.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteriophages / Virus Cultivation / Bioreactors / Cronobacter sakazakii Language: En Journal: J Microbiol Biotechnol Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteriophages / Virus Cultivation / Bioreactors / Cronobacter sakazakii Language: En Journal: J Microbiol Biotechnol Year: 2021 Document type: Article