Issue 48, 2017, Issue in Progress

Quantification analysis of protein and mycelium contents upon inhibition of melanin for Aspergillus niger: a study of matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS)

Abstract

Mass spectrometry (MS) provides a simple discrimination method for microorganisms. However, the presence of species such as melanin in fungal spores of Aspergillus niger (melanotic fungal) suppress ionization for matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Inhibition of melanin synthesis pathways by tricyclazole enhances mycelium growth and protein contents of Aspergillus niger for four different media; namely sabouraud dextrose agar medium (SDA), potato dextrose agar (PDA), czapek dox agar (CDA) and yeast extract agar (YEA) media. The cell contents of protein and mycelium growth of Aspergillus niger are increased with the addition of a low concentration of tricyclazole (25–50 mg L−1). Furthermore, it improves the ionization signals of A. niger for MALDI-MS. This study reveals that inhibition of melanin using tricyclazole leads to the increase of protein content, mycelium growth and enhanced peak signals of MALDI-MS.

Graphical abstract: Quantification analysis of protein and mycelium contents upon inhibition of melanin for Aspergillus niger: a study of matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS)

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2017
Accepted
19 May 2017
First published
12 Jun 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 30289-30294

Quantification analysis of protein and mycelium contents upon inhibition of melanin for Aspergillus niger: a study of matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS)

S. Kumaran, H. N. Abdelhamid and H. Wu, RSC Adv., 2017, 7, 30289 DOI: 10.1039/C7RA03741D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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