Early detection of fungal biomass on library materials |
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| Authors: | Nick R Konkol Christopher J McNamara Ethel Hellman Ralph Mitchell |
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| Institution: | 1. Laboratory of Applied Microbiology, School of Engineering and Applied Sciences, Harvard University, 40 Oxford St, Cambridge MA 02138, USA;2. Preservation and Imaging Department, Harvard College Libraries, Harvard University, Widener Library, Harvard Yard, Cambridge MA 02138, USA |
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| Abstract: | Library materials are susceptible to fungal deterioration. The paper constituents of archival materials are subjected to harmful physical and chemical processes as they are slowly consumed by fungi. Remediation of fungal contamination can be costly and risk further damage to fragile or previously degraded materials. Early detection of fungal growth would permit the use of relatively noninvasive treatments to remediate fungal contamination of artifacts before visible or lasting damage has occurred. Current methods used for the detection of microbial biomass, such as colony counts, microscopic biovolume estimation, and ergosterol analysis are expensive, time consuming, or are inappropriate for use with fungi. Beta-N-acetylhexosaminidase (EC 3.2.1.52) activity provides a rapid and reliable means of fungal detection on a variety of cultural heritage materials. Adapted for use on archival materials, fluorogenic 4-Methylumbelliferyl (MUF) labeled substrate N-acetyl-Beta-D-glucosamine (NAG) was used to detect fungal beta-N-acetylhexosaminidase activity. The fluorescence generated by minute quantities of fungi was quickly detected at an early stage of growth. The sensitivity of the assay was comparable to other biochemical techniques. The fluorometric assay was well-suited for early detection of fungal biomass on paper and assessment of the effectiveness of common remediation practices. |
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