Production and Partial Characterization of α-Amylase Enzyme from Marine Actinomycetes.

Amylase producing actinobacteria were isolated and characterized from terrestrial environment. There are a limited number of reports investigating the marine environment; hence, in the present study, four marine enzymes were tested for their amylase production ability. On starch agar plates, the Str...

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Publicado en:BioMed Research International pp. 1 - 16
Autores principales: Al-Agamy, Mohamed H., Alhuzani, Mohammad R., Kelany, Mahmoud S., Hamed, Moaz M.
Formato: equations & formulas pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 12/7/2021
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: BioMed Research International
      issn: 23146133
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      dt: 12/7/2021
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        154000346
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        154000346
        10.1155/2021/5289848
        154000346
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        atl: Production and Partial Characterization of α-Amylase Enzyme from Marine Actinomycetes.
      aug:
        au:
          Al-Agamy, Mohamed H.
          Alhuzani, Mohammad R.
          Kelany, Mahmoud S.
          Hamed, Moaz M.
        affil: Department of Pharmaceutics, College of Pharmacy, King Saud University, 11451 Riyadh 2457, Saudi Arabia
      sug:
        subj:
          Amylases Analysis
          Actinobacteria Analysis
          Human
          Cell Culture Techniques
          Electrophoresis Methods
          Culture Media
          Gram-Positive Bacteria
          Enzymes Physiology
          Descriptive Statistics
      ab: Amylase producing actinobacteria were isolated and characterized from terrestrial environment. There are a limited number of reports investigating the marine environment; hence, in the present study, four marine enzymes were tested for their amylase production ability. On starch agar plates, the Streptomyces rochei strain showed a higher hydrolytic zone (24 mm) than the other isolates. Growth under optimized culture conditions using Plackett-Burman's experimental design led to a 1.7, 9.8, 7.7, and 3.12-fold increase for the isolates S. griseorubens, S. rochei, S. parvus, and Streptomyces sp., respectively, in the specific activity measurement. When applying the Box-Behnken design on S. rochei using the most significant parameters (starch, K2HPO4, pH, and temperature), there was a 12.22-fold increase in the specific activity measurement 7.37 U/mg. The α-amylase was partially purified, and its molecular weight was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis. α-Amylase was particularly active at pH 6 and 65°C. The purified enzyme was most active at 65°C and pH 6, thermal stability of 70°C for 40 min, and salt concentration of 1 M with Km and Vmax of 6.58 mg/ml and 21.93 μmol/ml/min, respectively. The α-amylase was improved by adding Cu+2, Zn+2, and Fe+2 (152.21%, 207.24%, and 111.89%). Increased production of α-amylase enzyme by S. rochei KR108310 leads to production of significant industrial products.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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