Structural and functional analysis of a novel galactose-binding lectin derived from Chlorella sorokiniana MW769776
Document Type
Article
Publication Title
Journal of Biomolecular Structure and Dynamics
Abstract
A freshwater green microalgal strain was isolated and the lectin was identified in it by a strong hemagglutination activity (HA) assay. Characterization of the algal strain was found to be Chlorella sorokiniana (MW769776). A single step affinity chromatographic technique was developed to purify Chlorella sorokiniana lectin (CSL) using guar gum as the affinity matrix. The precipitate showed a single active peak with a titer value of 1024 HU, with a concentration of 1111 U, and a purification fold of 9. The purified protein exhibited a single band in SDS-PAGE with a molecular weight of 16 kDa. Analysis by liquid chromatography-electrospray ionization-quadrupole-time of flight mass spectrometry (LC-ESI-Q-TOF-MS) of tryptic-digested purified lectin showed that it was a monomeric protein. A multiple sequence alignment analysis revealed that the peptide sequences of CSL exhibited similarity with the H-type lectin domain of Micractinium conductrix. The structure of CSL was studied by FTIR and homology modeling methods, indicating the presence of α-helix as well as β-sheet in its secondary structure. Whereas the 3D structure exhibited the similarity with the core protein of light-harvesting reaction center complex of photosystem I. The significance of this study suggests that the characteristics of CSL are consistent with its identification as a hemagglutinin, a type of novel lectin, which suggests its candidature for various biological purposes. Communicated by Ramaswamy H. Sarma.
DOI
10.1080/07391102.2023.2274519
Publication Date
1-1-2023
Recommended Citation
Arekal, Roopashri N.; Savitha, J.; Kumar, Ashwini; and B. S, Gunashree, "Structural and functional analysis of a novel galactose-binding lectin derived from Chlorella sorokiniana MW769776" (2023). Open Access archive. 8869.
https://impressions.manipal.edu/open-access-archive/8869