The salt preservation method has been used for a long time in the leather industries with salt applied to raw skins and hides in order to control bacterial activity and to remove the moisture found in the skin structure. It is known that the salt used in curing process contains many halophilic bacterial species. During the salting process, skins and hides might be contaminated with these micro-organisms. The goal of this research was to determine factors including the pH of salt samples, total count of haloversatile bacteria, proteolytic haloversatile bacteria, and lipolytic haloversatile bacteria found in these samples and to isolate, and identify haloversatile bacteria from the salt samples, to test their ability to use various amino acid and sugar sources, to characterise their enzymatic properties, to investigate their adverse effects on sheepskinand goatskin samples using a scanning electron microscopy. In addition, 2.5A direct electric current was applied against mixed culture of enzymeproducing haloversatile bacteria in 15% NaCl solution to search for an alternative environmentally friendly preservation method for skin/hide curing. The pH values of salt samples were found to be between 7.60 and 8.04.
The total counts of haloversatile bacteria, proteolytic haloversatile bacteria and lipolytic haloversatile bacteria were found to be 6 × 103CFU/g to 1.3 × 105CFU/g; 1×103-7×103CFU/g and 1.4 × 103-3.1 × 104CFU/g, respectively. 35 haloversatile bacteria belonging to ten different genera (Staphylococcus, Corynebacterium, Peribacillus, Lysinibacillus, Kocuria, Paenibacillus, Bhargavaea, Bacillus, Pseudomonas and Micrococcus) were isolated and identified from the salt samples. The ability of haloversatile bacteria to use sugars and amino acids varied from one genus to another genus. While catalase, esterase, urease, protease, caseinase, lipase, xylanase, cellulase, amylase, DNase and oxidase enzymes were produced among the isolates, pullulanase enzyme was not produced.
The scanning electron microscope micrographs showed that enzyme-producing haloversatile bacteria had significant effects on goatskin and sheepskin. The total number of the mixed culture was reduced from 3.6 × 106CFU/mL to 4×101CFU/mL within 17 minutes, and all cells were completely killed within 21 minutes. The scanning electron micrographs showed that the structure and the organoleptic characterictics of bacteria treated sheepskin and goatskin samples were negatively changed at the end of 40-days storage.
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