Salting‐out extraction of recombinant κ‐carrageenase and phage T7 released from Escherichia coli cells

Abstract: Traditional technology of cell disruption has become one of the bottlenecks restricting the industrialization of genetic engineering products due to its high cost and low efficiency. In this study, a novel bioprocess of phage lysis coupled with salting‐out extraction (SOE) was evaluated. The lysis effect of T7 phage on genetically engineered Escherichia coli expressing κ‐carrageenase was investigated at different multiplicity of infection (MOI), meanwhile the phage and enzyme released into the lysate were separated by SOE. It was found that T7 phage could lyse 99.9% of host cells at MOI = 1 and release more than 90.0% of enzyme within 90 min. After phage lysis, 87.1% of T7 phage and 71.2% of κ‐carrageenase could be distributed at the middle phase and the bottom phase, respectively, in the SOE system composed of 16% ammonium sulfate and 20% ethyl acetate (w/w). Furthermore, κ‐carrageenase in the bottom phase could be salted out by ammonium sulfate with a yield of 40.1%. Phage lysis exhibits some advantages, such as mild operation conditions and low cost. While SOE can efficiently separate phage and intracellular products. Therefore, phage lysis coupled with SOE is expected to become a viable alternative to the classical cell disruption and intracellular product recovery.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Salting‐out extraction of recombinant κ‐carrageenase and phage T7 released from Escherichia coli cells ; day:17 ; month:05 ; year:2023 ; extent:10
Engineering in life sciences ; (17.05.2023) (gesamt 10)

Creator
Chen, Da
Dong, Yue‐Sheng
Bao, Yong‐Ming
Xiu, Zhi‐Long

DOI
10.1002/elsc.202200125
URN
urn:nbn:de:101:1-2023051815065958034986
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:58 AM CEST

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Associated

  • Chen, Da
  • Dong, Yue‐Sheng
  • Bao, Yong‐Ming
  • Xiu, Zhi‐Long

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