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Reduction of hexavalent chromium by Ochrobactrum intermedium BCR400 isolated from a chromium-contaminated soil

机译:分离自铬污染土壤的中间O鱼BCR400还原六价铬

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摘要

Hexavalent chromium-resistant BCR400 was isolated from chromium contaminated soil collected from Vadodara, Gujarat. It reduced 100 mg Cr(VI)/L completely in 52 h with initial Cr(VI) reduction rate of 1.98 mg/L/h. The Cr(VI) reduction rate decreased with increase in Cr(VI) concentration from 100 to 500 mg/L. The addition of anthraquinone-2-sulphonic acid (AQS) to culture BCR400 significantly enhanced its chromium reduction rate. The activation energy of AQS-mediated Cr(VI) reduction (120.69 KJ/mol) was 1.1-fold lower than non-mediated Cr(VI) reduction. An increase in the activities of quinone reductase and chromate reductase in cells grown in presence of AQS/AQS + Cr(VI) suggests their role in reduction of Cr(VI) by . Both chromate reductase and quinone reductase activities were FAD independent, required NADH as reductant, displayed maximum activity at pH (7.0) and temperature (30 °C). Thus Cr(VI) bioremediation potential of can be enhanced by augmentation of system with AQS as redox mediator.
机译:从古吉拉特邦的瓦多达拉(Vadodara)收集的铬污染土壤中分离出六价抗铬BCR400。它在52小时内完全还原了100 mg Cr(VI)/ L,初始Cr(VI)还原速率为1.98 mg / L / h。 Cr(VI)的还原速率随Cr(VI)浓度从100毫克/升增加到500毫克/升而降低。向BCR400培养物中添加蒽醌-2-磺酸(AQS)可以显着提高其铬还原率。 AQS介导的Cr(VI)还原的活化能(120.69 KJ / mol)比非介导的Cr(VI)还原低1.1倍。在AQS / AQS + Cr(VI)存在下生长的细胞中醌还原酶和铬酸还原酶活性的增加表明它们在Cr还原Cr(VI)中的作用。铬酸还原酶和醌还原酶的活性都不依赖于FAD,需要NADH作为还原剂,在pH(7.0)和温度(30°C)时显示最大活性。因此,可以通过以AQS作为氧化还原介体的系统的增强来增强Cr(VI)的生物修复潜力。

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