Clinical-type dextran: A review on process and enzyme engineering strategies to control molecular weight distribution [Klinisches Dextran: Dextran vom klinischen Typ: Ein Überblick über verfahrens- und enzymtechnische Strategien zur Kontrolle der Molekulargewichtsverteilung]

Pia Lanvers, Jannis Bröker, Jochen Schmid

Review article (journal) | Peer reviewed

Abstract

Dextrans are α-(1 → 6)-linked, mostly branched α-d-glucopyranosyl polysaccharides synthesized from sucrose by lactic acid bacteria. The unique properties of dextrans, their biocompatibility, biodegradability, and non-immunogenicity support a wide range of medical and industrial applications. Key characteristics of dextran, including solubility, viscosity, and molecular weight, highly depend on the bacterial strain and the conditions under which it is synthesized. The structural diversity within the family of dextran-synthesizing enzymes contributes to dextran diversity. Conventionally, dextran with low molecular weight is obtained by fermentative production of high molecular weight dextran, followed by partial hydrolysis and a precise fractionation procedure, which is a costly and hazardous process. However, recent advances in enzyme- and bioprocess engineering in combination with analytical techniques have significantly enhanced the ability to control the molecular weight and branching patterns of dextran. Thereby improving its effectiveness and broadening its applications in both industrial and clinical settings. This review focuses on the production of dextrans with defined molecular weight and the enzymatic mechanisms underlying their synthesis, which have been increasingly studied in recent years. In particular, clinical-type dextran with a molecular weight of 70 kDa is of high commercial value and scientific interest.

Details about the publication

JournalCarbohydrate Polymers
Volume364
Article number123783
StatusPublished
Release year2025 (22/05/2025)
Language in which the publication is writtenEnglish
DOI10.1016/j.carbpol.2025.123783
Link to the full texthttps://www.sciencedirect.com/science/article/pii/S0144861725005661?via%3Dihub
KeywordsClinical-type dextran; Molecular weight; Bioprocess engineering; Enzymatic catalysis; Downstream processing; Regulatory specifications

Authors from the University of Münster

Lanvers, Pia
Professorship of Microbiology (Prof. Schmid)
Schmid, Jochen
Professorship of Microbiology (Prof. Schmid)