Pattanapipitpaisal P, Mabbett A N, Finlay J A, Beswick A J, Paterson-Beedle M, Essa A, Wright J, Tolley M R, Badar U, Ahmed N, Hobman J L, Brown N L, Macaskie L E
School of Biosciences, The University of Birmingham, Edgbaston, UK.
Environ Technol. 2002 Jul;23(7):731-45. doi: 10.1080/09593332308618367.
Resistance to Cr(VI) is usually associated with its cellular exclusion, precluding enrichment techniques for the isolation of organisms accumulating Cr(VI) via bioreduction to insoluble Cr(III). A technique was developed to screen for potential Cr(VI) reduction in approx. 2000 isolates from a coastal environment, based on the non-specific reduction of selenite and tellurite to Se0 and Te0, and reduction of tetrazolium blue to insoluble blue formazan. The most promising strains were further screened in liquid culture, giving three, which were identified by 16S rRNA sequence analysis as Bacillus pumilus, Exiguobacterium aurantiacum and Pseudomonas synxantha, all of which reduced 100 microM Cr(VI) anaerobically, without growth. The respective removal of Cr(VI) was 90% and 80% by B. pumilus and E. aurantiacum after 48 h and 80% and by P. synxantha after 192 h. With the gram positive strains Cr(VI) promoted loss of flagella and, in the case of B. pumilus, lysis of some cells, but Cr was deposited as an exocellular precipitate which was identified as containing Cr and P using energy dispersive X-ray microanalysis (EDAX). This prompted the testing of Citrobacter sp. N14 (subsequently re-assigned by 16S rRNA sequence analysis and biochemical studies as a strain of Serratia) which bioprecipitates metal cation phosphates via enzymatically-liberated phosphate. This strain reduced Cr(VI) at a rate comparable to that of P. synxantha but Cr(III) was not bioprecipitated where La(III) was removed as LaPO4, even though a similar amount of phosphate was produced in the presence of Cr(III). Since B. pumilus removed most of the Cr(VI), with the formation of cell-bound CrPO4 implicated, this suggests that this strain could have future bioprocess potential.
对六价铬的抗性通常与其细胞外排有关,这使得通过生物还原将六价铬积累为不溶性三价铬的生物体的富集技术难以实现。基于亚硒酸盐和亚碲酸盐非特异性还原为Se0和Te0以及四唑蓝还原为不溶性蓝色甲臜,开发了一种技术来筛选来自沿海环境的约2000株分离物中潜在的六价铬还原能力。对最有潜力的菌株进行液体培养进一步筛选,得到了三株,通过16S rRNA序列分析鉴定为短小芽孢杆菌、橙色栖热菌和类黄假单胞菌,它们在无氧条件下均能还原100 microM的六价铬,且不生长。短小芽孢杆菌和橙色栖热菌在48小时后对六价铬的去除率分别为90%和80%,类黄假单胞菌在192小时后对六价铬的去除率为80%。对于革兰氏阳性菌株,六价铬会导致鞭毛丧失,在短小芽孢杆菌的情况下,还会导致一些细胞裂解,但铬以细胞外沉淀的形式沉积,使用能量分散X射线微分析(EDAX)鉴定该沉淀含有铬和磷。这促使对柠檬酸杆菌N14进行测试(随后通过16S rRNA序列分析和生化研究重新分类为沙雷氏菌属的一个菌株),该菌通过酶促释放的磷酸盐生物沉淀金属阳离子磷酸盐。该菌株还原六价铬的速率与类黄假单胞菌相当,但在镧以磷酸镧形式被去除的情况下,三价铬未被生物沉淀,尽管在三价铬存在时产生了相似量的磷酸盐。由于短小芽孢杆菌去除了大部分六价铬,并涉及形成细胞结合的磷酸铬,这表明该菌株可能具有未来生物工艺潜力。