The main goal of the current study is to biosynthesize titanium dioxide nanoparticles (TiO₂-NPs) using green approach to biocontrol of different fungal strains isolated from historical Description of Egypt book. Nineteen fungal strains were isolated from deteriorated parts and identified by the traditional and molecular methods as Aspergillus flavus (8-isolates), Aspergillus versicolor (2-isolates), Aspergillus ustus (4-isolates), Aspergillus chinensis (2-isolates), Penicillium citrinum (2-isolates), and Penicillium chrysogenum (1-isolate). These fungal strains showed high cellulase, amylase, pectinase, and gelatinase activities which have a significant role in biodeterioration. The biomass filtrate of probiotic strain, Lactobacillus rhamnosus, was used to fabricate TiO₂-NPs which characterized by UV-Vis, FT-IR, XRD, TEM, SEM, EDX, DLS, and zeta potential. The obtained data showed the successful formation of spherical and anatase phase NPs with sizes of 3–7 nm and zeta potential values of – 19.9 and – 36.8 mV. The main components of as-formed nanomaterial were Ti and O with weight percentages of 55.91 and 46.25, respectively. The biocompatibility of synthesized TiO₂-NPs was investigated toward two normal cell lines, WI38 and HFB4, which reveal the low toxicity at high concentrations (IC₅₀ > 300 μg mL^–1). Therefore, concentrations ≤ 300 μg mL^–1 were used to biocontrol of isolated fungi. Data showed the promising activity of various concentrations (300, 200, and 100 μg mL^–1) of TiO₂-NPs to inhibit the growth of fungal strains with varied inhibition zones and dose-dependent manner. This study exhibited the efficacy of probiotic bacterial strains in the synthesis of TiO₂-NPs that can be used to preserve historical books from fungal deterioration. Graphical

This study aims to assess the deterioration aspects of a historical manuscript dating back to the 14th century that was deposited in the Library of the Arabic Language Academy, Cairo, Egypt. The study aims at the exploration of the role of various fungal strains that had colonized this deteriorated manuscript in its biodeterioration through their efficacy in the secretion of various hydrolytic enzymes. To evaluate the deterioration, various techniques, including visual inspection, attenuated total reflectance Fourier transform infrared (ATR-FTIR), scanning electron microscopy (SEM), X-Ray diffraction analysis (XRD), color change, and pH value, were utilized. The fungal strains linked to the historical document were isolated, identified, and evaluated for their deterioration activities. The findings demonstrate that the manuscript exhibits a variety of deterioration signs including color change, brittleness and weakness, erosion, and removal of the grain surface pattern in leather binding. According to the ATR-FTIR, the chemical composition of the historical paper and leather underwent some alterations. The historical paper has a lower level of cellulose crystallinity than the control sample. Penicillium chrysogenum (two isolates), P. citrinum (four isolates), Aspergillus ustus (three isolates), A. terreus (two isolates), A. chinensis (one isolate), Paecilomyces sp. (one isolate), and Induratia sp. (one isolate) were among the fourteen fungal strains identified as being associated with the historical manuscript. These fungal strains produced several hydrolytic enzymes with high activity, such as cellulase, amylase, gelatinase, and pectinase, which play a key role in biodegradation.

This study focuses on the efficacy of silver nitrate (AgNO₃) as a coating agent used to preserve papers against microbial deterioration. To this end, the in vitro cytotoxicity of AgNO₃ was assessed against two normal cell lines, WI-38 and HFB-4, to detect a safe dose that can be used as a coating agent, which was 80 µg mL⁻¹. Bacillus subtilis B3 and Penicillium chrysogenum F9 were selected as high deteriorating microbes, previously isolated from a historical manuscript dating back to 1677 A.-D. The microbial growth inhibition, color change, mechanical properties, and cellulosic fibers of untreated/treated papers were evaluated. The data showed the efficacy of AgNO₃ to inhibit the growth of B. subtilis with a percentage of 100% after 7 days, while it inhibits the growth of P. chrysogenum with a percentage of 85.9 ± 1.1% after 21 days. The color and mechanical properties of treated paper in the presence/absence of microbial inoculation were slightly changed, although they changed greatly due to microbial growth in the absence of AgNO₃. The EDX analysis confirmed the successful adsorption of Ag-ion on papers, with a weight percentage of 1.9%. The cellulosic fibers of untreated paper in the presence of microbial growth were highly deteriorated as compared with treated and standard filter paper (shown by FT-IR and SEM).

Herein, the deteriorating aspects of a historical manuscript (papers and leather bookbinding) dated back to the 17^th century were evaluated with reference to the role of the associated fungal communities. The deterioration signs were investigated using visual assessment, SEM, ATR-FTIR, XRD, color changes, and pH values compared with control. Data showed that the most deterioration aspects were represented by the dust, dirt, erosion, stains, bores, weakness, missed parts, decreasing in paper crystallinity, shifting of wavenumbers of cellulosic band, and changing of color and pH. The dependent-culturable technique showed that thirteen fungal strains were associated with historical manuscript and identified using traditional and molecular methods as Aspergillus niger (three isolates), A. fumigatus (two isolates), A. quadrilineatus (three isolates), Penicillium citrinum (two isolates), and P. chrysogenium (three isolates). These fungal strains showed high efficacy to secretion various hydrolytic enzymes including cellulase, amylase, gelatinase, and pectinase which play a critical role in biodeterioration.