Unravelling the dominant role of phosphorylation degree in governing the functionality of reassembled casein micelles: Implications for future dairy production through precision fermentation
Artikel i vetenskaplig tidskrift, 2025

This study investigated the effect of bovine casein (CN) phosphorylation degree on micelle reassembly, stability, calcium-binding, and acid-induced gelation or precipitation, with the aim of assessing the feasibility of utilising microbial CNs in future dairy production. The four CNs (αS1-, αS2-, β-, and κ-CN) were purified from bovine milk and subjected to enzymatic dephosphorylation, resulting in three pools – fully and partially phosphorylated and fully dephosphorylated. Nine reassembled CN micelle solutions (RCMS) were investigated, consisting of three systems (two of four-CN, and one of β/κ-CN) and three phosphorylation degrees of the corresponding CNs. The distribution of different components (protein, calcium, and phosphorus) into micellar, serum, and insoluble fractions after two centrifugation steps was studied. The pH stability relative to acid-gelation or precipitation of the formed RCMS was further investigated. Results showed that the micelle reassembly ability of RCMS containing all four CNs was proportional to the phosphorylation degree; CNs with higher phosphorylation degrees contained a higher proportion of micelles and exhibited greater calcium-binding ability, whereas fully dephosphorylated CNs hardly formed CN micelle structures. The gelation pH of RCMS increased with decreasing phosphorylation degree, whereas the fully dephosphorylated CNs completely failed in gelation but precipitated when reaching their isoelectric point at pH 5.5. Moreover, RCMS containing only β/κ-CN at their native full phosphorylation were unstable at the salt concentrations applied, with more than half of the CNs self-associating to flocculate. Our study confirms the essential role of phosphorylation degree in micelle reassembly and stability, providing important information for potential future applications of microbial CNs that are expected to exhibit non-native phosphorylation levels.

Acid-induced gelation

TEM

Calcium-binding ability

Reassembled casein micelles

Dephosphorylation

Författare

Jing Che

Aarhus Universitet

Zekun Fan

Wageningen University and Research

Etske Bijl

Wageningen University and Research

Julia Prangchat Stub Thomsen

Aarhus Universitet

Ivan Mijakovic

Chalmers, Life sciences, Systembiologi

Novo Nordisk Fonden

Kasper Hettinga

Wageningen University and Research

Nina Aagaard Poulsen

Aarhus Universitet

Lotte Bach Larsen

Aarhus Universitet

Food Hydrocolloids

0268-005X (ISSN)

Vol. 159 110615

Är Bacillus subtilis PtkA reglerad som ett "cyclin-dependant" kinas?

Vetenskapsrådet (VR) (2020-03176), 2021-01-01 -- 2024-12-31.

Ämneskategorier

Fysikalisk kemi

DOI

10.1016/j.foodhyd.2024.110615

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Senast uppdaterat

2024-09-20