Adsorption of Remazol Brilliant Violet-5R from Aqueous Solution Using Sugarcane Bagasse as Biosorbent: Kinetic and Thermodynamic Studies

Sugarcane bagasse is an inexpensive and eco-friendly natural biosorbent for the removal of various organic pollutants. The adsorption of Remazol Brilliant Violet-5R (RBV-5R) dye on sugarcane bagasse (SCB) was studied. Biosorbent was characterized using EDX and FTIR. The effect of various experimental parameters, such as pH, biosorbent dosage, initial dye concentration, contact time, adsorption with shaking and without shaking, and the temperature, was optimized. At pH 6, maximum biosorption of 92.22% was achieved using 0.15 g of SCB. The equilibrium was attained within 30–40 min for the removal of RBV-5R. The initial dye concentration of 10 µg/mL was determined as an optimum concentration for maximum removal of RBV-5R at 30 °C. Langmuir and Freundlich adsorption isotherms were applied, and it was found that the biosorption of RBV-5R follows Freundlich adsorption isotherms. Kinetic studies were also carried out and it was found that the proposed method followed the pseudo-second-order kinetic model (R2 = 0.98). From desorption study, it was found that maximum desorption in the increasing order was obtained using ethanol, methanol, and 0.2 M sodium hydroxide (NaOH). The biosorption study was applied to actual textile waste effluent to pave way for the practical usage of this technology on a larger scale and the results were found effective

Adsorption of Remazol Brilliant Violet-5R from Aqueous Solution Using Sugarcane Bagasse as Biosorbent: Kinetic and Thermodynamic Studies

Sugarcane bagasse is an inexpensive and eco-friendly natural biosorbent for the removal of various organic pollutants. The adsorption of Remazol Brilliant Violet-5R (RBV-5R) dye on sugarcane bagasse (SCB) was studied. Biosorbent was characterized using EDX and FTIR. The effect of various experimental parameters, such as pH, biosorbent dosage, initial dye concentration, contact time, adsorption with shaking and without shaking, and the temperature, was optimized. At pH 6, maximum biosorption of 92.22% was achieved using 0.15 g of SCB. The equilibrium was attained within 30–40 min for the removal of RBV-5R. The initial dye concentration of 10 µg/mL was determined as an optimum concentration for maximum removal of RBV-5R at 30 °C. Langmuir and Freundlich adsorption isotherms were applied, and it was found that the biosorption of RBV-5R follows Freundlich adsorption isotherms. Kinetic studies were also carried out and it was found that the proposed method followed the pseudo-second-order kinetic model (R2 = 0.98). From desorption study, it was found that maximum desorption in the increasing order was obtained using ethanol, methanol, and 0.2 M sodium hydroxide (NaOH). The biosorption study was applied to actual textile waste effluent to pave way for the practical usage of this technology on a larger scale and the results were found effective

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees

This study aimed to find the molecular basis of Bardet-Biedl syndrome (BBS) in Pakistani consanguineous families. A total of 12 affected families were enrolled. Clinical investigations were performed to access the BBS-associated phenotypes. Whole exome sequencing was conducted on one affected individual from each family. The computational functional analysis predicted the variants’ pathogenic effects and modeled the mutated proteins. Whole-exome sequencing revealed 9 pathogenic variants in six genes associated with BBS in 12 families. The BBS6/MKS was the most common BBS causative gene identified in five families (5/12, 41.6%), with one novel (c.1226G>A, p.Gly409Glu) and two reported variants. c.774G>A, Thr259LeuTer21 was the most frequent BBS6/MMKS allele in three families 3/5 (60%). Two variants, c.223C>T, p.Arg75Ter and a novel, c. 252delA, p.Lys85STer39 were detected in the BBS9 gene. A novel 8bp deletion c.387_394delAAATAAAA, p. Asn130GlyfsTer3 was found in BBS3 gene. Three known variants were detected in the BBS1, BBS2, and BBS7 genes. Identification of novel likely pathogenic variants in three genes reaffirms the allelic and genetic heterogeneity of BBS in Pakistani patients. The clinical differences among patients carrying the same pathogenic variant may be due to other factors influencing the phenotype, including variants in other modifier genes

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees

This study aimed to find the molecular basis of Bardet-Biedl syndrome (BBS) in Pakistani consanguineous families. A total of 12 affected families were enrolled. Clinical investigations were performed to access the BBS-associated phenotypes. Whole exome sequencing was conducted on one affected individual from each family. The computational functional analysis predicted the variants’ pathogenic effects and modeled the mutated proteins. Whole-exome sequencing revealed 9 pathogenic variants in six genes associated with BBS in 12 families. The BBS6/MKS was the most common BBS causative gene identified in five families (5/12, 41.6%), with one novel (c.1226G>A, p.Gly409Glu) and two reported variants. c.774G>A, Thr259LeuTer21 was the most frequent BBS6/MMKS allele in three families 3/5 (60%). Two variants, c.223C>T, p.Arg75Ter and a novel, c. 252delA, p.Lys85STer39 were detected in the BBS9 gene. A novel 8bp deletion c.387_394delAAATAAAA, p. Asn130GlyfsTer3 was found in BBS3 gene. Three known variants were detected in the BBS1, BBS2, and BBS7 genes. Identification of novel likely pathogenic variants in three genes reaffirms the allelic and genetic heterogeneity of BBS in Pakistani patients. The clinical differences among patients carrying the same pathogenic variant may be due to other factors influencing the phenotype, including variants in other modifier genes