Author:
Sheladiya Priyanka,Kapadia Chintan,Prajapati Vimal,Ali El Enshasy Hesham,Abd Malek Roslinda,Marraiki Najat,Zaghloul Nouf S. S.,Sayyed R. Z.
Abstract
AbstractPectate lyase is a hydrolytic enzyme used by diverse industries to clarify food. The enzyme occupies a 25% share of the total enzyme used in food industries, and their demand is increasing gradually. Most of the enzymes in the market belong to the fungal origin and take more time to produce with high viscosity in the fermentation medium, limiting its use. The bacteria belonging to the genus Bacillus have vast potential to produce diverse metabolites of industrial importance. The present experiment aimed to isolate pectate lyase-producing bacteria that can tolerate an alkaline environment at moderate temperatures. Bacillus subtilis PKC2, Bacillus licheniformis PKC4, Paenibacillus lactis PKC5, and Bacillus sonorensis ADCN produced pectate lyase. The Paenibacillus lactis PKC5 gave the highest protein at 48 h of incubation that was partially purified using 80% acetone and ammonium sulphate. Purification with 80% acetone resulted in a good enzyme yield with higher activity. SDS-PAGE revealed the presence of 44 kDa molecular weight of purified enzyme. The purified enzyme exhibits stability at diverse temperature and pH ranges, the maximum at 50 °C and 8.0 pH. The metal ions such as Mg2+, Zn2+, Fe2+, and Co2+ significantly positively affect enzyme activity, while increasing the metal ion concentration to 5 mM showed detrimental effects on the enzyme activity. The organic solvents such as methanol and chloroform at 25% final concentration improved the enzyme activity. On the other hand, detergent showed inhibitory effects at 0.05% and 1% concentration. Pectate lyase from Paenibacillus lactis PKC5 had Km and Vmax values as 8.90 mg/ml and 4.578 μmol/ml/min. The Plackett–Burman and CCD designs were used to identify the significant process parameters, and optimum concentrations were found to be pectin (5 gm%) and ammonium sulphate (0.3 gm%). During incubation with pectate lyase, the clarity percentage of the grape juice, apple juice, and orange juice was 60.37%, 59.36%, and 49.91%, respectively.
Publisher
Springer Science and Business Media LLC
Reference56 articles.
1. Gummadi, S. N. & Panda, T. Purification and biochemical properties of microbial pectinases—a review. Process Biochem. 38, 987–996. https://doi.org/10.1016/S0032-9592(02)00203-0 (2003).
2. Ramakanth, N.V., Anuradha, K., & Naga Padma, P. Alkaline polygalacturonases from thermotolerant pectinolytic bacteria from diverse sources. Int. J. Sci. Res. Publ. 4, 2250–3153 (2014). www.ijsrp.org.
3. Taper, A. R. & Jain, R. K. Pectinases: enzymes for fruit processing industry. Int. Food Res. J. 21, 447–453 (2014).
4. Sun, L. & van Nocker, S. Analysis of promoter activity of members of the PECTATE LYASE-LIKE (PLL) gene family in cell separation in Arabidopsis. BMC Plant Biol. 10, 152. https://doi.org/10.1186/1471-2229-10-152 (2010).
5. Tariq, A. & Latif, Z. Isolation and biochemical characterization of bacterial isolates producing different levels of polygalacturonases from various sources. Afr. J. Microbiol. Res. 6, 7259–7264. https://doi.org/10.5897/AJMR12.923 (2012).
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献