Search

A deacidifying/antifungal mixture composed of calcium propionate, methylparaben and propylparaben was tested against Aspergillus niger , Cladosporium cladosporioides , Chaetomium globosum , Penicillium chrysogenum and Penicillium corylophilum . The preventive treatment of paper samples resulted in a complete fungal growth inhibition on 4 of the 5 tested species. The antifungal properties of the formulation remained unaffected for a minimum period of one year. The disinfecting treatment with the mixture led to a total elimination of all tested fungal species. The effects of the tested formulation on paper were evaluated in terms of pH, colourimetry, folding endurance, FTIR and XRD, using moist heat artificial ageing. Aside from plain paper, paper previously colonized by A. niger was tested to evaluate the potential of the formulation in preventing deterioration caused by fungal metabolites. In plain paper, an effective deacidification and long-term prevention of mechanical resistance loss were achieved, although a slight paper discoloration occurred. On previously colonized by fungi, the treatment effectively prevented the deterioration caused by fungal metabolites. [ABSTRACT FROM AUTHOR]

Volumes from an archive of the University of Milan showed whitish-grey discolouration putatively caused by microorganisms. Microscopic and viability assays proved that discolouration from two volumes were characterized by a marked presence of viable fungi, demonstrating that they were mainly biological in nature. Fungal sequences were phylogenetically most closely related to Eurotium , Aspergillus , Candida , Penicillium , Alternaria , Phaeosphaeria , Capnodiales and Pleosporales taxa. SEM analysis showed that Eurotium halophilicum is dominant on the two infected volumes. Viable airborne fungal loads near the two volumes were higher than recommended maximum values, demonstrating that airborne fungi could represent a source of risk. The airborne microbial community sampled in two different seasons was composed by fungi belonging in the genera Aspergillus , Candida and Eurotium . The detection of E. halophilicum also in the archival air indicated a possible source of contamination. Fluctuations of thermo-hygrometric values were also observed in the archive in the different seasons. The occurrence of white efflorescence on the stored volumes most likely depended on the lack of both a dusting programme and air-conditioning, and insufficient ventilation in the repository, and, on the hygroscopic behaviour of the binding materials used in the manufacture of the volumes. [ABSTRACT FROM AUTHOR]

In the past, the animal glues were used in paper manufacturing and in restoration of artworks preserved in museums, libraries and archives. By ageing they went through deterioration creating distortions, tensions, cockling and discolouration in paper materials. Consequently, the removal of glue residues becomes an essential step in the restoration of ancient and artwork paper material. Current mechanical and chemical methods display serious drawbacks mainly related to aggressiveness towards material or toxicity for restorers. Bio-based methods for paper cleaning rely on the use of enzymes that require skilled operators, optimal application conditions and high costs, creating difficulties in mastering enzyme use so far. This paper describes a first attempt of biocleaning ancient paper from organic deposits using living bacteria. The non-pathogenic, non-spore-forming and non-cellulolytic original strain Ochrobactrum sp. TNS15 E was successfully applied -immobilised in an agar gel-on original paper specimens dating back to the 17th. After 4 h of contact with the bacterial pack, the cellulose fibres underlying glue were disclosed, highlighting the bacterial capacity of removing the glue layer without damaging the paper or leaving undesirable residues. Both colorimetry and SEM analyses proved the results. The procedure is simple, low-cost and safe for the artefact, the restorers and the environment. [ABSTRACT FROM AUTHOR]

In order to examine the potential efficacy of simultaneous dual-species fungal treatment of wood for lignocellulosic ethanol production, whole organism fungal biopulping methods utilizing white rot ( Ceriporiopsis subvermispora ) and brown rot ( Postia placenta ) fungi alone or in co-culture were compared for effect on wood microstructure, chemical composition, and enzymatic sugar solubilization. Liriodendron tulipifera wood chips exposed for 30 days to C . subvermispora and/or P . placenta fungi alone or in co-culture exhibited qualitative differences in wood microstructure, but did not significantly differ in final percent composition of holocellulose, α -cellulose, or lignin content compared to controls. All fungal treatments increased the soluble reducing sugar yield of enzymatic hydrolysis by ca. 28–30% over sterile controls. The co-culture fungal treatment did not significantly differ in reducing sugar yield compared to monoculture treatments, suggesting an unexpected lack of additive or other synergistic species effects on wood degradation using these fungi in co-culture. Paired interaction agar plate assays demonstrated that C . subvermispora and P . placenta exhibited mutual distance-mediated growth inhibition that was independent of substrate type or availability, suggesting an explanation for the observed lack of degradative synergy between these taxa. This study is the first to report the effects of simultaneous co-treatment with white and brown rot fungi, highlights the need for further optimization of methods to account for specialized fungal degradative mechanisms, and examines the potential influence of competitive interactions in whole-organism biopulping treatments utilizing different taxa. [ABSTRACT FROM AUTHOR]

Abstract: Fungi are among the most degradative organisms inducing biodeterioration of paper-based items of cultural heritage. Appropriate conservation measures and restoration treatments to deal with fungal infections include mechanical, chemical, and biological methods, which entail effects on the paper itself and health hazards for humans. Three different conservation treatments, namely freeze-drying, gamma rays, and ethylene oxide fumigation, were compared and monitored to assess their short- (one month, T1) and long-term (one year, T2) effectiveness to inhibit fungal growth. After the inoculation with fungi possessing cellulose hydrolysis ability — Chaetomium globosum, Trichoderma viride, and Cladosporium cladosporioides — as single strains or as a mixture, different quality paper samples were treated and screened for fungal viability by culture-dependent and -independent techniques. Results derived from both strategies were contradictory. Both gamma irradiation and EtO fumigation showed full efficacy as disinfecting agents when evaluated with cultivation techniques. However, when using molecular analyses, the application of gamma rays showed a short-term reduction in DNA recovery and DNA fragmentation; the latter phenomenon was also observed in a minor degree in samples treated with freeze-drying. When RNA was used as an indicator of long-term fungal viability, differences in the RNA recovery from samples treated with freeze-drying or gamma rays could be observed in samples inoculated with the mixed culture. Only the treatment with ethylene oxide proved negative for both DNA and RNA recovery. Therefore, DNA fragmentation after an ethylene oxide treatment can hamper future paleogenetic and archaeological molecular studies on the objects. [Copyright &y& Elsevier]

Abstract: Fungal melanin staining is a problem on many cultural objects, ranging from the French Palaeolithic cave at Lascaux to books and papers in museum collections. Melanin, because it is insoluble and resistant to bleaching, may leave behind undesirable stains long after the fungal infestation has been controlled. Research into removal of melanin stains from paper and other sensitive substrates using industrial biomimetic oxidizing systems has shown considerable success. We studied relative concentration of the bleaching reagents and the reaction kinetics both in liquid suspensions of melanin and on melanized paper samples. Liquid suspension samples were tested for changes in their chemical composition (appearance and relative representation of functional groups and chemical bonds) with FTIR spectrometry. Changes in color of melanized paper samples were investigated with a CIE L*a*b system, where the effectiveness of the treatment (bleaching) was determined as a change in lightness (ΔL). Melanin was oxidized in the liquid suspensions, and the intensity of modification depended on the procedure employed. Bleaching of melanin with the biomimetic copper–pyridine complex proved to be far superior to the effect of white-rot fungal oxidizing enzymes, previously reported on by this group. [Copyright &y& Elsevier]

Abstract: Since its invention, paper has become one of the main carriers of our cultural, scientific, political, economic and historical information. Given the importance of this material, its preservation is a matter of great interest. Paper can be deteriorated due to physical, chemical and biological agents. Within microorganisms, fungi are the major paper biodeteriogens. Throughout history, several methods have been used to prevent and stop fungal deterioration on paper based materials. In this work we present a review of the main chemical and physical methods used to avoid fungal paper biodeterioration until nowadays and also of some new approaches tested recently. The advantages and disadvantages of these methods are discussed as well as their health effects. Studies regarding antifungal compositions, methods of application, performance and effects on the treated materials are also presented with the aim of providing a clear set of conclusions on the topic. [Copyright &y& Elsevier]

Abstract: The small rusty stains (foxing) frequently found on historic paper documents, books, and prints have generally been analysed in the past by optical microscope through their morphochromatic appearance under visible light and UV radiation. Despite increased research efforts with more sophisticated techniques (mainly SEM and XRF), the biotic or even chemical origin of these stains remains unclear. The purpose of this paper is to verify to what extent a simple technique such as FTIR-ATR spectroscopy can be utilised for a clearer understanding of the controversial nature of foxing. Since this technique is sensitive to several organic chemical groups that are in common with both fungi and gelatine-sized ancient paper, some modern cardboards stained by biotic foxing have been selected for the analyses. The results clearly show the importance of FTIR and mycological analyses for the identification of residual microfungal agents, together with the by-products of their activity on paper substrates. [Copyright &y& Elsevier]

Abstract: The growth of molds on paper containing cellulose is a frequent occurrence when the level of relative air humidity is high or when books become wet due to water leaks in libraries. The aim of this study is to differentiate the bioreceptivity of different types of book paper for different fungi. Laboratory tests were performed with strains of Aspergillus niger, Cladosporium sp., Chaetomium globosum and Trichoderma harzianum isolated from books. Four paper types were evaluated: couché, Pólen (offset), recycled and a reference paper containing only cellulose. The tests were carried out in chambers with relative air humidity of 95% and 100%. Mold growth was greatest in the tests at 100% relative humidity. Results of stereoscopic microscopy observation showed that Cladosporium sp. grew in 74% of these samples, A. niger in 75%, T. harzianum in 72% and C. globosum in 60%. In the chambers with 95% air humidity Cladosporium sp. grew in only 9% of the samples, A. niger in 1%, T. harzianum in 3% and C. globosum did not grow in any sample. The most bioreceptive paper was couché and the least receptive was recycled paper. The composition of the recycled paper, however, varies depending on the types of waste materials used to make it. [Copyright &y& Elsevier]

Abstract: A sample set of model graded papers containing known organic and inorganic components was used to culture an Aspergillus terreus strain able to produce acidic metabolites and cellulolytic enzymes. This study set out to document the biogenic formation of calcium oxalate crystals, as a consequence of fungal activity and growth, on a range of paper samples. Scanning electron microscopy and FTIR spectroscopy techniques were employed to achieve this end. Bioleaching processes induced by fungi on carbonate used in the manufacture of paper, together with the capacity of fungi to produce – very rapidly – significant biogenesis of monohydrate and dihydrate calcium oxalate crystals on the surface of papers, were investigated. SEM images of calcium containing paper samples disclosed a very clear difference in the pattern of inorganic material distribution when areas spoiled by fungi and those not affected by fungal growth were compared. In addition, the FTIR spectrum of CaCO3 sized paper clearly demonstrated, following fungal growth, the FTIR absorbance of fungus and calcium oxalate, together with the disappearance of carbonate bands. [Copyright &y& Elsevier]

Abstract: Biofilm formation in papermaking processes could inflict financial loss by interrupting paper machine operation and pose a potential health hazard. A mixed microbial culture obtained from paper machine slime and a Pseudomonas strain (identified as Pseudomonas putida HB45) which is tolerant to the alkyl dimethyl benzyl ammonium chloride (quaternary ammonium chloride, QAC) were used to investigate the interplay between disinfectants and glucose on bacterial growth and biofilm formation. QAC and 2,2-dibromo-3-nitrilopropionamide (DBNPA) were found to be effective at concentration lower than isothiazolone in both standardized Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) tests. Crystal violet staining technique demonstrated that biofilm formation of P. putida HB45 and the mixed culture could be controlled by modest dosage of DBNPA and QAC; however, they could be barely eliminated due to high MBC to MIC ratios. In simulated papermaking processing water, glucose was shown to increase the average biofilm formation rates during stationary phase for both P. putida HB45 and the mixed culture under the presence of biocides. Complexity and population diversity of biofilm of the paper machine slime was observed by in-situ cryo-scanning electron microscopy. Confocal laser scanning microscopy (CSLM) was employed to show qualitative and partial quantitative biofilm formation under various circumstances. The results of this study could assist improving strategy for controlling biofilm formation in papermaking processes. [Copyright &y& Elsevier]

Abstract: With many important artistic works and documents made of paper, and thus susceptible to biodeterioration by fungi, research is required in an effort to replace toxic chemical products with other more benign ones. In this work the antifungal effect of methyl and propyl paraben mixtures at different concentrations was evaluated. The fungi used in the experiments were a Cladosporium species and Penicillium corylophilum, both of which are well known as paper-biodeteriorating fungi. The results demonstrate that a mixture of 0.5% methyl paraben and 1% propyl paraben, in 85% ethanolic solution, is the lowest concentration necessary to provide an efficient antifungal action. A deacidification agent, 5% calcium propionate, was added to this mixture to produce a multi-purpose formulation to treat acidification and fungal contamination of paper documents. Tests carried out on paper samples before and after application of this mixture showed only a minor increase in yellowing and a slight decrease in tensile strength, while substantially raising the pH, and thus the alkaline reserve, and also a slight increase in the percentage of deformation. [Copyright &y& Elsevier]

Abstract: In this paper we deliver a report on the study of microbiological damage found on the pages of a 16th-century book. Our aim is to describe the procedures needed to ensure a conservative approach to the restoration of valuable books and objects of art made from, or supported on, paper. The techniques employed to evaluate and describe the damage observed, as well as the organisms responsible for biodeterioration, are discussed. A range of sampling techniques and instruments were utilised, including swabs and adhesive tape. Conventional methods, such as classic culturing and the direct microscopic observation of sampled material, were coupled with DNA-fingerprinting and phylogenetic analysis. We postulated that the purple stains which migrate through the pages with a felted consistency (Fig. 2), based on all the information obtained using traditional and molecular means, were caused by a cellulolytic fungus producing purple essudates, characterised by echinated conidia and Hülle cells. These elements were consistent with the discovery of both A. versicolor and A. nidulans using molecular techniques. [Copyright &y& Elsevier]

Studies were carried out in vitro on a cellulose based agar at two water activities (aw,0.975,0.995) and on three types of paper at two relative humidities (75, 100% RH) for the potential for differentiation of contamination and colonisation by Aspergillus terreus, A. holandicus and Eurotium chevalieri. In vitro studies showed that conducting polymer sensor array gave different responses to each of these species when grown on cellulose agar at both aw levels. Discriminant function analyses of the data showed differentiation of the controls from the spoilage fungi. Cluster analysis gave a significant (P=0.05) separation of the control and each spoilage fungus. In situ studies on three types of paper showed that using natural substrates the volatile patterns produced by each of these fungi was different from each other and from the control. The results obtained were better at the higher humidity. The three paper types could be successfully differentiated into clusters. For a single paper type, differentiation of controls from spoilage fungal treatments was better at the higher humidity. This study has shown that this technology has potential for the early detection of fungal contamination in library materials and archives for the improved protection of cultural heritage. [Copyright &y& Elsevier]

Commercially available paper, flax, glass wool and rock wool insulation materials were tested for sensitivity to moisture and the ability of fungi to grow on them under different moisture regimes. Three levels of moisture were used, ambient, simulated rain and water holding capacity. After wetting, the materials were inoculated with a mixture of fungi and incubated at 26°C in boxes with high moisture levels for 4 weeks. The greatest degree of fungal growth was observed on paper and flax insulation materials initially conditioned to ambient moisture levels. Paper and flax insulation were strongly affected by moisture, with all treatments showing losses in dry mass of approx. 20%, except for paper subjected to simulated rain treatment in which the loss was 39%. Glass and rock wools were not sensitive to moisture and were resistant to fungal degradation, showing only traces of fungal growth and minimal loss in dry mass over 4 weeks. [Copyright &y& Elsevier]

After initial tests carried out on 20 stained paper samples from different centuries, we have devised a non-destructive method for taking samples from foxed areas of ancient maps. The stains were examined in normal light (NL) and then with fluorescence; we then checked whether fungal colonies were not developing in areas that did not respond to electronic excitation. Samples were taken using gauze–cotton swabs from fluorescent areas only. We found that fungi did develop, in the areas of the paper samples that were not clearly visible (NL) but fluorescent, when they were placed inside humidity chambers. It was confirmed that there is a correlation between the thermo-hygrometric parameters and the place of preservation and a relationship between the environment and the fungal species. We found cellulosolithic fungi and bacteria. We recommend early identification of “discolouring” with fluorescent methods in order to arrange suitable thermo-hygrometric conditions for preventing development of the infection. [Copyright &y& Elsevier]

Modern building materials, once moistened, may provide ecological niches for various microbes that have not been well characterized. The aim of the current study was to determine whether fungal genera and actinobacteria were associated with seven types of moisture-damaged building materials by systematically describing the mycobiota and enumerating fungi and bacteria in these materials. Microbial analyses were obtained from 1140 visibly damaged samples of building material, viz. wood, paper, non-wooden building boards, ceramic products, mineral insulation materials, paints and glues, and plastics. Fungal and bacterial concentrations correlated well (r=0.6). The range of fungi and bacteria numbers was between 100 and 108 cfu g−1 in all materials, but significant differences in counts were observed between materials. Highest median concentrations of fungi were observed in wooden and paper materials, and lowest in samples of mineral insulation, ceramic products, and paints and glues. Concentrations of viable bacteria in mineral insulation materials were significantly lower than in wood, paper, ceramic products and plastics. A rich variety of fungi was found in wooden materials, with Penicillium and yeasts occurring most frequently. In paper materials, a clear difference from wood was the more frequent occurrence of Cladosporium and Stachybotrys. The most distinctive finding in gypsum boards was that Stachybotrys was common. Ceramic products and paints and glues seemed to favour Acremonium and Aspergillus versicolor. Yeasts and members of the Sphaeropsidales occurred often in parallel in most materials. This study confirms that microbial growth occurs in many different building materials and shows associations between fungal genera and the type of material. [Copyright &y& Elsevier]