Enzymatic decolorization of bacterial pigments from culturally significant marble

Marble monuments and facades are susceptible to microbial colonization. Microbial growth on a marble surface can develop into unsightly red stains whose removal has proven problematic. The purpose of this study was to determine if the red-brown stains on Isamu Noguchi's marble sculpture Slide Mantra (1991) could be caused by pigment-producing microorganisms and to assess the potential of enzymatic stain remediation. Traditional cell culture methods were used to isolate a pigmented bacterium from a stained area of the sculpture. Sequencing and analysis of the 16S rRNA gene identified the organism as a strain of Serratia marcescens, and FT-IR spectroscopy demonstrated that the pigment produced by the bacteria was most likely a prodigiosin. Decolorization of the pigment in solution demonstrated that the enzyme laccase from the fungus Trametes versicolor has potential as a decolorizing agent. This study suggests that enzymatic decolorization may be applicable to stains on culturally significant marble caused by microbial colonization.     

Ferrography

A new process is described which we have named “Ferrography.” The process enables graphic information to be recorded on magnetic materials and to be reproduced on paper in visual form. Magnetic inks are available in black or colors, enabling monochrome or color reproductions to be made. The magnetic matrix may be used repeatedly so that multiple printing is possible, and the matrix may be stored indefinitely. The process has advantages: economy and speed of operation, permanence of image, and ability to record any information which is available in signal form, such as instrument data, facsimile transmission, or scanned images.     

Protection from extinction provided by a conditioned inhibitor

Three conditioned suppression experiments with rats as subjects investigated the influence of higher order associations in determining the response potential of a target stimulus. In these experiments, a Pavlovian conditioned inhibitor was compounded with the target cue during extinction treatment. In Experiment 1, strong suppression was observed to the target cue that was given extinction treatment in the presence of a conditioned inhibitor, relative to a target that was extinguished with an associatively neutral cue or was extinguished alone, suggestive of enhanced protection from extinction provided by a conditioned inhibitor. This effect was replicated in a sensory preconditioning preparation in Experiment 2; in Experiment 3, in a sensory preconditioning preparation, this protection effect was retroactively attenuated when the conditioned excitor used to train the conditioned inhibitor was extinguished following extinction of the target. This provides evidence that, at least in a sensory preconditioning preparation, stimuli that are only indirectly associated with the target cue can contribute to the response potential of that target.     

Early detection of fungal biomass on library materials

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.