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1.
Spectrochim Acta A Mol Biomol Spectrosc ; 317: 124359, 2024 Sep 05.
Article in English | MEDLINE | ID: mdl-38704996

ABSTRACT

SERS (Surface Enhanced Raman Spectroscopy) is a new Raman spectroscopy which relies on Surface Plasmon Resonance (SPR) of metal nanoparticles. We have applied colloidal silver and gold nanoparticles as amplifier agents to enhance nucleotide Raman signals. It is observed that without these enhancing agents, it is impossible to investigate nucleotide spectrum due to weak Raman signals. Interaction mechanism of Melphalan, an anticancer drug with four nucleotides (Adenine, Cytosine, Guanine, Thymine) was investigated using SERS to detect and identify changes due to alkylating process in Raman spectra. After incubating Melphalan drug with nucleotides for 24 h at 37 °C, some changes occurred in SERS spectrum and interpretation of SERS spectra revealed the influence of the alkyl substitution on peaks and Raman shifts. After incubation of Melphalan with each nucleotide, intensity of relevant SERS signals assigned to Amid III group of Cytosine and Amid I of Thymine decreased significantly, confirming alkylating taking place. In this study, we also investigated the effect of nanoparticles type on nucleotide spectrum. We could not obtain useful information in the cases of guanine nucleotide. The SERS spectrum of Cytosine as an example of nucleotides in aqueous solution compared to solid state and results demonstrated that in solid state better signals were obtained than in liquid state.


Subject(s)
Melphalan , Metal Nanoparticles , Nucleotides , Spectrum Analysis, Raman , Spectrum Analysis, Raman/methods , Melphalan/chemistry , Nucleotides/chemistry , Metal Nanoparticles/chemistry , Gold/chemistry , Alkylating Agents/chemistry , Silver/chemistry
2.
J Biotechnol ; 150(3): 366-71, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20869403

ABSTRACT

A complete system for on-line sampling, sample handling and analysis of fermentation processes has been set up. The system is designed such that a sample is taken from the fermentor, the metabolism of microbial cells is instantaneously arrested, the cells are lysed in order to release intracellular compounds and in a subsequent binding assay the content of target molecules is monitored. The system is constructed based on the flow-injection analysis concept. Good agreement between on-line analysis and off-line analysis is reported.


Subject(s)
Bioreactors , Biotechnology/methods , Fermentation , Flow Injection Analysis/methods , Recombinant Fusion Proteins , Escherichia coli/growth & development , Escherichia coli/metabolism , Intracellular Space , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/metabolism , Temperature , beta-Glucosidase/biosynthesis , beta-Glucosidase/metabolism
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