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Optimization of cultural conditions of Arthrobacter sp. Sphe3 for growth-associated chromate(Ⅵ) reduction in free and immobilized cell systems

机译:关节杆菌菌种培养条件的优化。 Sphe3用于减少游离和固定细胞系统中生长相关的铬酸盐(Ⅵ)

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摘要

The current study aimed to characterize Arthrobacter sp. Sphe3 ability to reduce Cr(Ⅵ) in suspended cell cultures as well as in immobilized form using Ca-alginate beads. Adaptation studies in the presence of 5 mg L~(-1) Cr(Ⅵ) showed a significant increase in specific growth rate from 0.25 to 0.3 h~(-1) and bioremoval percentage from 64% to 94% (p<0.05), whereas Arthrobacter sp. Sphe3 could tolerate up to 50 mg L~(-1) Cr(VI). Optimization of culture conditions resulted in complete reduction of 45 mg L~(-1) Cr(VI) at 30 ℃, pH 8 and 10g L~(-1) of glucose. High glucose concentrations helped at reducing (80 ±2.4)% of initial 100 mg L~(-1) Cr(Ⅵ), whereas the bacterial strain could tolerate 850 mg L~(-1) Cr(Ⅵ). Cr(Ⅲ) formation was first evidenced by the appearance of a green insoluble precipitate in the medium. Cell biomass was successfully immobilized in Ca-alginate beads that were evaluated for their stability. Cell release was sharply decreased when 4% Na-alginate was used under non-shaking conditions. Biotransformation efficiency was enhanced when 25-50 mg cells mL~(-1) Na-alginate from the exponential growth phase were collected and co-encapsulated with either 1% glucose and 0.5% (NH_4)_2SO_4, or 1% LB medium. Immobilized biocat-alyst could be reused up to 6 continuous cycles in the presence of 10 mg L~(-1) Cr(Ⅵ), but its performance was lowered at higher metal concentrations comparing with free cells that significantly maintained their reducing ability up to 300 mg L~(-1) Cr(Ⅵ).
机译:当前的研究旨在表征节杆菌。 Sphe3能够在悬浮细胞培养物中以及使用钙藻酸盐微珠固定化形式还原Cr(Ⅵ)的能力。在5 mg L〜(-1)Cr(Ⅵ)存在下的适应性研究表明,比生长速率从0.25 h〜(-1)显着提高,生物去除率从64%升高至94%(p <0.05) ,而节杆菌属Sphe3最多可耐受50 mg L〜(-1)Cr(VI)。优化培养条件可在30℃,pH 8和10g L〜(-1)葡萄糖条件下完全还原45 mg L〜(-1)Cr(VI)。高浓度葡萄糖有助于降低初始100 mg L〜(-1)Cr(Ⅵ)的(80±2.4)%,而细菌菌株可以耐受850 mg L〜(-1)Cr(Ⅵ)。 Cr(Ⅲ)的形成首先通过在介质中出现绿色不溶性沉淀来证明。细胞生物量已成功固定在钙藻酸盐珠中,对其稳定性进行了评估。在非振动条件下使用4%海藻酸钠时,细胞释放急剧减少。当收集来自指数生长期的25-50 mg细胞mL〜(-1)海藻酸钠并与1%葡萄糖和0.5%(NH_4)_2SO_4或1%LB培养基共包封时,生物转化效率得到提高。固定化的生物催化剂在10 mg L〜(-1)Cr(Ⅵ)的存在下可以重复使用多达6个连续循环,但与游离细胞相比,在高金属浓度下其性能降低了,后者显着地保持了还原能力。 300 mg L〜(-1)Cr(Ⅵ)。

著录项

  • 来源
    《Chemosphere》 |2014年第1期|535-540|共6页
  • 作者单位

    Department of Chemical Engineering. Section of Chemistry, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece;

    Department of Chemistry, University ofloannina, loannina 45110, Greece;

    Department of Chemical Engineering. Section of Chemistry, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Bioreduction; Chromium; Arthrobacter; Immobilization; Alginate;

    机译:生物还原铬;关节杆菌固定;海藻酸盐;

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