Humphries A C, Nott K P, Hall L D, Macaskie L E
School of Biosciences, The University of Birmingham, Edgbaston, B15 2TT, UK.
Biotechnol Lett. 2004 Oct;26(19):1529-32. doi: 10.1023/B:BILE.0000044457.80314.4d.
Growth-decoupled cells of Desulfovibrio vulgaris NCIMB 8303 can be used to reduce Pd(II) to cell-bound Pd(0) (Bio-Pd(0)), a bioinorganic catalyst capable of reducing hexavalent chromium to less toxic Cr(III), using formate as the electron donor. Magnetic resonance imaging showed that Bio-Pd(0), immobilized in chitosan and agar beads, is distinguishable from the surrounding gel and is evenly dispersed within the immobilization matrix. Agar-immobilized Bio-Pd(0) and 'chemical Pd(0)' were packed into continuous-flow reactors, and challenged with a solution containing 100 microM Cr(VI) (pH 7) at a flow rate of 2.4 ml h(-1). Agar-immobilized chemical Pd(0) columns lost Cr(VI) reducing ability by 160 h, whereas columns containing immobilized Bio-Pd(0) maintained 90% reduction until 680 h, after which reduction efficiency was gradually lost.
普通脱硫弧菌NCIMB 8303的生长解耦细胞可用于将Pd(II)还原为细胞结合的Pd(0)(生物Pd(0)),这是一种生物无机催化剂,能够以甲酸盐作为电子供体将六价铬还原为毒性较小的Cr(III)。磁共振成像显示,固定在壳聚糖和琼脂珠中的生物Pd(0)与周围凝胶可区分开,并均匀分散在固定化基质中。将琼脂固定的生物Pd(0)和“化学Pd(0)”填充到连续流动反应器中,并以2.4 ml h(-1)的流速用含有100 microM Cr(VI)(pH 7)的溶液进行挑战。琼脂固定的化学Pd(0)柱在160小时后失去了Cr(VI)还原能力,而含有固定化生物Pd(0)的柱在680小时之前保持90%的还原率,此后还原效率逐渐丧失。