TY - JOUR
T1 - Fungal surface protein mediated one-pot synthesis of stable and hemocompatible gold nanoparticles
AU - Kitching, Michael
AU - Choudhary, Priyadarshani
AU - Inguva, Saikumar
AU - Guo, Yina
AU - Ramani, Meghana
AU - Das, Sujoy K.
AU - Marsili, Enrico
N1 - Funding Information:
M. Kitching was funded by IRCSET (Ireland) , Project ID RS/2012/276. SK Das acknowledges Council of Scientific and Industrial Research (CSIR), Govt. of India for financial support under STRAIT programme. P. Choudhary gratefully acknowledges Department of Science and Technology (DST), Govt. of India for INSPIRE fellowship. We also thank Rajani Vijayaraghavan for XRD analysis of the AuNPs.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Despite their large secretome and wide applications in bioprocesses, fungi remain underexplored in metal nanoparticles (MNP) biosynthesis. Previous studies have shown that cell surface proteins of Rhizopus oryzae play a crucial role in biomineralization of Au(III) to produce gold nanoparticles (AuNPs). Therefore, it is hypothesized that purified cell surface protein may produce in vitro AuNPs with narrow size distribution for biomedical and biocatalytic applications. However, different protein extraction methods might affect protein stability and the AuNP biosynthesis process. Herein, we have explored the extraction of cell surface proteins from R. oryzae using common detergents and reducing agent (sodium dodecyl sulfate (SDS) Triton X-100, and 1,4-dithiothreitol (DTT)) and their effect on the size and shape of the biosynthetic AuNPs. The surface proteins extracted with reducing agent (DTT) and non-ionic detergent (Triton X-100) produce spherical AuNPs with a mean particle size of 16 ± 7 nm, and 19 ± 4 nm, respectively, while the AuNPs produced by the surface protein extracted by ionic detergent (SDS) are flower-like AuNPs with broader size distribution of 43 ± 19 nm. This synthetic approach does not require use of any harsh chemicals, multistep preparation and separation process, favouring environmental sustainability. The biosynthetic AuNPs thus formed, are stable in different physiological buffers and hemocompatible, making them suitable for biomedical applications.
AB - Despite their large secretome and wide applications in bioprocesses, fungi remain underexplored in metal nanoparticles (MNP) biosynthesis. Previous studies have shown that cell surface proteins of Rhizopus oryzae play a crucial role in biomineralization of Au(III) to produce gold nanoparticles (AuNPs). Therefore, it is hypothesized that purified cell surface protein may produce in vitro AuNPs with narrow size distribution for biomedical and biocatalytic applications. However, different protein extraction methods might affect protein stability and the AuNP biosynthesis process. Herein, we have explored the extraction of cell surface proteins from R. oryzae using common detergents and reducing agent (sodium dodecyl sulfate (SDS) Triton X-100, and 1,4-dithiothreitol (DTT)) and their effect on the size and shape of the biosynthetic AuNPs. The surface proteins extracted with reducing agent (DTT) and non-ionic detergent (Triton X-100) produce spherical AuNPs with a mean particle size of 16 ± 7 nm, and 19 ± 4 nm, respectively, while the AuNPs produced by the surface protein extracted by ionic detergent (SDS) are flower-like AuNPs with broader size distribution of 43 ± 19 nm. This synthetic approach does not require use of any harsh chemicals, multistep preparation and separation process, favouring environmental sustainability. The biosynthetic AuNPs thus formed, are stable in different physiological buffers and hemocompatible, making them suitable for biomedical applications.
KW - Gold nanoparticles
KW - Nanobiosynthesis
KW - Protein extraction
UR - http://www.scopus.com/inward/record.url?scp=84996538263&partnerID=8YFLogxK
U2 - 10.1016/j.enzmictec.2016.08.007
DO - 10.1016/j.enzmictec.2016.08.007
M3 - Article
C2 - 27866629
AN - SCOPUS:84996538263
SN - 0141-0229
VL - 95
SP - 76
EP - 84
JO - Enzyme and Microbial Technology
JF - Enzyme and Microbial Technology
ER -