Abstract

Animal hides are one of man’s earliest and mostly used materials; many rawhide products, primarily leather, have for centuries been used for several purposes. The peculiar mechanical properties of leather depend on the hide composition, a dense collagen feltwork. Unfortunately, due to their proteic composition, rawhides may undergo microbial attack and biodeterioration. Over centuries, different processes and treatments (brining, vegetal or chrome tanning, tawing, etc.) were set up to face the biological attack and modify/stabilise the hide’s mechanical properties. Nevertheless, even present-day rawhides are subjected to biological colonisation, and traces of this colonisation are clearly shown in Chrome(III) tanned leathers (in the wet blue stage), with obvious economic damages. The colonisation traces on tanned leathers consist of isolated or coalescent red patches, known as red heat deterioration. Parchments are rawhide products, too; they derive from another manufacturing procedure. Even parchments undergo microbial attack; the parchment biodeterioration seems comparable to leather red heat deterioration and is known as purple spots. Recently, an ecological succession model explained the process of historical parchment purple spot deterioration; the haloarchaea Halobacterium salinarum is the pioneer organism triggering this attack. The marine salt used to prevent rawhide rotting is the carrier of haloarchaea colonisers (Migliore et al., 2019). The aim of this study was to investigate the dynamics of biodeterioration on Chrome(III) tanned leathers and its effects on the stability/integrity of collagen structure. To this end, standard cultivation methods were integrated with three updated technologies, Next-Generation Sequencing (NGS), Raman spectroscopy, and Light Transmitted Analysis (LTA). A bioinformatic comparison between chrome tanned leather vs. historical parchment colonisers was performed to evaluate if leather and parchment share common culprits; furthermore, the effect of the biodeterioration on the physical properties of the hide product was evaluated.

Highlights

  • Almost all human cultures have exploited the unique properties of rawhide for millennia, developing specialised techniques to take profit from this readily available material

  • The reference strain (H. salinarum DSM 3754), NaClPOTECO salt-cured rawhides (BRH + NaClPOTECO; sheep rawhide (SRH) + NaClPOTECO) and NaClPOTECO alone gave positive cultures; no growth was observed for NaClLAB salt-cured rawhides (SRH + NaClLAB) and for chrome tanned leather (DTL; undamaged tanned leather (UTL)) samples (Supplementary Figure S2)

  • bovine rawhide (BRH) yielded 549,285 microbial sequences assigned to 1,661 operational taxonomic units (OTUs), TABLE 1 | Bovine rawhides (BRHs), red damaged tanned leathers (DTLs), and undamaged tanned leathers (UTLs) sample yields from each replicate (#1, 2, 3)

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Summary

Introduction

Almost all human cultures have exploited the unique properties of rawhide for millennia, developing specialised techniques to take profit from this readily available material. These properties depend on its complex structure, consisting predominantly of a dense collagen fibre network. Chrome(III) tanning is the present-day dominant method in leather manufacturing (Saxena et al, 2017); chrome tanned leather has extraordinary stability after washing, an excellent softness, fullness and elasticity for making leather products (Ward, 1974; Zhang et al, 2017). These special features have substantially contributed to the success of the leather industry

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