Impact of the number of rhamnose moieties of rhamnolipids on the structure, lateral organization and morphology of model biomembranes.

Soft Matter

Physical Chemistry I - Biophysical Chemistry, Faculty of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn Street 4a, 44227 Dortmund, Germany.

Published: March 2021


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Various studies have described remarkable biological activities and surface-active properties of rhamnolipids, leading to their proposed use in a wide range of industrial applications. Here, we report on a study of the effects of monorhamnolipid RhaCC and dirhamnolipid RhaRhaCC incorporation into model membranes of varying complexity, including bacterial and heterogeneous model biomembranes. For comparison, we studied the effect of HAA (CC, lacking a sugar headgroup) partitioning into these membrane systems. AFM, confocal fluorescence microscopy, DSC, and Laurdan fluorescence spectroscopy were employed to yield insights into the rhamnolipid-induced morphological changes of lipid vesicles as well as modifications of the lipid order and lateral membrane organization of the model biomembranes upon partitioning of the different rhamnolipids. The partitioning of the three rhamnolipids into phospholipid bilayers changes the phase behavior, fluidity, lateral lipid organization and morphology of the phospholipid membranes dramatically, to what extent, depends on the headgroup structure of the rhamnolipid, which affects its packing and hydrogen bonding capacity. The incorporation into giant unilamellar vesicles (GUVs) of a heterogeneous anionic raft membrane system revealed budding of domains and fission of daughter vesicles and small aggregates for all three rhamnolipids, with major destabilization of the lipid vesicles upon insertion of RhaCC, and also formation of huge GUVs upon the incorporation of RhaRhaCC. Finally, we discuss the results with regard to the role these biosurfactants play in biology and their possible impact on applications, ranging from agricultural to pharmaceutical industries.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d0sm01934hDOI Listing

Publication Analysis

Top Keywords

model biomembranes
12
organization morphology
8
lipid vesicles
8
three rhamnolipids
8
rhamnolipids
5
impact number
4
number rhamnose
4
rhamnose moieties
4
moieties rhamnolipids
4
rhamnolipids structure
4

Similar Publications

Order parameters in membranes: Following Joachim Seelig's path.

Biochim Biophys Acta Biomembr

August 2025

Institut Européen de Chimie et Biologie, Univ. Bordeaux, CNRS, INSERM, IECB, US1, UAR 3033, F-33600 Pessac, France; Institute of Chemistry & Biology of Membranes & Nanoobjects, Univ. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, F-33600 Pessac, France. Electronic address:

Following the publication of biological membrane models in the 1970s, Joachim Seelig was the first to experimentally demonstrate the dynamic nature of these membranes. He conducted the first ssNMR experiments to measure the order parameters of the CD (H) bond of lipids deuterium-labelled, showing a fairly fluid membrane interior. Since then, the order parameters of the CD, CH and CC bonds have been measured.

View Article and Find Full Text PDF

Efficient Sampling of Free Energy Landscapes for the Calculation of Protein-Protein Binding Affinities in Membranes.

J Phys Chem B

September 2025

Department of Chemistry, Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215, United States.

The accurate simulation of realistic biomembranes is a long-term goal in the field of membrane biophysics. Efforts to simulate increasingly complex lipid bilayers, consisting of multiple lipid types and proteins, have been hindered by the shortcomings of current force fields, both coarse-grained and all-atom, in the modeling of protein-protein and protein-lipid interactions. Due to the fundamental importance of protein dimerization to cellular signaling and protein trafficking, the study of protein-protein association and the related dimerization free energies has received significant attention in both simulations and experiments.

View Article and Find Full Text PDF

Modulation of TNAP activity and apatite formation in biomimetic matrix vesicles studied by P solid-state NMR.

Biochim Biophys Acta Biomembr

August 2025

Department of Chemistry, Faculty of Philosophy, Sciences and Letters at Ribeirão Preto, University of São Paulo, Brazil. Electronic address:

Skeletal and dental mineralization relies on a precisely regulated sequence of events culminating in apatite deposition onto collagen fibrils. Matrix vesicles (MVs), extracellular vesicles released by mineralization-competent cells, play a pivotal role in this process through the catalytic activity of alkaline phosphatase (TNAP). The lipid composition of MVs, particularly phosphatidylserine (PS)-calcium complexes, facilitates the nucleation of amorphous calcium phosphate and apatite formation.

View Article and Find Full Text PDF

Determination of the Mechanisms of Terbium(III) Biosorption by Strains with Adsorption Selectivity for Heavy Rare Earth Elements.

Microorganisms

July 2025

Jiangxi Provincial Key Laboratory of Environmental Pollution Prevention and Control in Mining and Metallurgy, Ganzhou 341000, China.

species have shown the potential to recover rare earth elements (REEs), but strains with adsorption selectivity for terbium(III) remain understudied. In this study, six strains with the capability for efficient adsorption of Tb(III) were screened from an ionic rare earth mine and were identified based on 16S rRNA gene sequencing. Adsorption experiments showed that sp.

View Article and Find Full Text PDF

Intrinsic disorder (ID) in proteins is a complex phenomenon, encompassing a continuum from entirely disordered regions to structured domains with flexible segments. The absence of a ground truth for all forms of disorder, combined with the possibility of structural transitions between ordered and disordered states under specific conditions, makes accurate prediction of ID especially challenging. The Critical Assessment of Protein Intrinsic Disorder (CAID) evaluates ID prediction methods using diverse benchmarks derived from DisProt, a manually curated database of experimentally validated annotations.

View Article and Find Full Text PDF