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The detrimental effects of inorganic and organic synthetic flocculants on humans and their recalcitrance in the environment have necessitated the search for safe, eco-friendly alternatives, including microbial flocculants. A bioflocculant-producing bacteria was isolated from sediment samples of Algoa Bay in the Eastern Cape Province of South Africa. The bacteria was identified through partial 16S ribosomal ribonucleic acids (rRNA), nucleotide sequencing, and BLAST analysis of the gene sequence that showed the bacteria to have 98% similarity to Bacillus algicola strain QD43 and deposited in GenBank as Bacillus sp. AEMREG7 with accession number KF933697.1. The effect of culture conditions on MBF-UFH production revealed optimally at inoculum size of 3% (v/v), glucose, a mixed nitrogen source [NH4 (SO4)2 + urea + yeast extract], and pH 6 for inoculums size, carbon and nitrogen sources, and initial medium pH for the fermentation process, respectively. The spent culture broth-rich bioflocculant attained the highest flocculating activity of 88.5% after 72 h of fermentation during the exponential phase of bacterial growth. It showed a high flocculating activity for kaolin clay suspension over a wide pH range of 4-10 with maximum flocculating activity observed at pH 6; and also retained 70.5% flocculating activity after heating at 100ºC for 60 min. These findings suggest that MBF-UFH has a great potential to substitute hazardous chemical flocculants commonly used in water treatment, hence reducing deformities among individuals in society.
Lignocellulosic materials are potential sources of isolating bacteria that can be used to produce important value-added products such as cellulase (endoglucanase) and xylanase in industry. Based on the above-mentioned premise, this study aimed to assess endoglucanase and xylanase-degrading potentials of a bacterial isolate from decaying sawdust samples collected from a wood factory at Melani village, Nkonkobe Municipality of Eastern Cape Province, South Africa. The bacteria showed high activity for endoglucanase and xylanase when grown on carboxymethyl cellulose (CMC) and birch wood xylan as sole carbon sources, respectively. The bacterial isolate was identified through 16S rDNA sequencing and the gene sequence was found to have 98% similarity with that of Chryseobacterium taichungense. The sequence was deposited in the GenBank as Chrysobacterium taichungense SAMRC-UFH2 with accession number KU171370. Optimum culture conditions for endoglucanase and xylanase production included: pH 6, incubation temperature (25ºC), and agitation rates of 50 rpm and 150 rpm for endoglucanase and xylanase, respectively. The high enzyme activities exhibited by this bacterial strain portend it as a potentially relevant candidate as a producer for value-added products of biotechnological importance.
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