Manohar S, Kim C K, Karegoudar T B
Department of Biochemistry, Gulbarga University, India.
Appl Microbiol Biotechnol. 2001 Apr;55(3):311-6. doi: 10.1007/s002530000488.
A Pseudomonas sp. strain NGKI (NCIM 5120) capable of degrading naphthalene was immobilized in polyurethane foam. The naphthalene-degrading activity of the freely suspended cells was compared with that of immobilized cells in batches in shaken culture and in a continuous culture system in a packed-bed reactor. Increasing concentrations of naphthalene were better tolerated and more quickly degraded by immobilized cell cultures than by free cells. An initial naphthalene concentration of 25 mM was completely degraded by freely suspended cells (4 x 10(10) cfu ml(-1)) and polyurethane-foam-immobilized cells (0.8-1 x 10(12) cfu g(-1) foam cubes) after 4 days and 2 days of incubation, respectively. Free cells degraded a maximum of 30 mM naphthalene after 4 days of incubation with 50 mM naphthalene, and no further degradation was observed even after 15 days of incubation, whereas foam-immobilized cells brought about the complete degradation of 50 mM initial naphthalene after 6 days of incubation. Furthermore, with 25 mM naphthalene, the polyurethane-foam-immobilized cells were re-used 45 times over a period of 90 days without losing naphthalene-degrading activity. By contrast, with the same amount of naphthalene, alginate-, agar-, and polyacrylamide-entrapped cells could be reused for 18, 12, and 23 times over a period of 44, 28, and 50 days, respectively. During continuous degradation in a packed-bed reactor, foam-immobilized cells degraded 80 mM naphthalene at a rate of 150 ml(-1) h(-1). With the same flow rate and 40 mM naphthalene, this system operated efficiently and continuously for about 120 days, whereas the packed-bed reactor with alginate-, agar-, and polyacrylamide-entrapped cells could be operated only for 45, 40, and 60 days respectively. Thus, more efficient degradation of naphthalene could be achieved by immobilizing cells of Pseudomonas sp. strain NGK1 in polyurethane foam, rather than in the other matrices tested.
一株能够降解萘的假单胞菌属菌株NGKI(NCIM 5120)被固定在聚氨酯泡沫中。将游离悬浮细胞和固定化细胞在摇瓶培养的分批培养以及填充床反应器的连续培养系统中对萘的降解活性进行了比较。与游离细胞相比,固定化细胞培养物能够更好地耐受并更快地降解浓度不断增加的萘。初始萘浓度为25 mM时,游离悬浮细胞(4×10¹⁰ cfu ml⁻¹)和聚氨酯泡沫固定化细胞(0.8 - 1×10¹² cfu g⁻¹泡沫方块)分别在培养4天和2天后将其完全降解。游离细胞在与50 mM萘一起培养4天后最多降解30 mM萘,即使培养15天后也未观察到进一步降解,而泡沫固定化细胞在培养6天后实现了50 mM初始萘的完全降解。此外,对于25 mM萘,聚氨酯泡沫固定化细胞在90天内可重复使用45次而不丧失萘降解活性。相比之下,对于相同量的萘,藻酸盐、琼脂和聚丙烯酰胺包埋的细胞分别在44天、28天和50天内可重复使用18次、12次和23次。在填充床反应器的连续降解过程中,泡沫固定化细胞以150 ml⁻¹ h⁻¹的速率降解80 mM萘。在相同流速和40 mM萘的条件下,该系统高效连续运行约120天,而含有藻酸盐、琼脂和聚丙烯酰胺包埋细胞的填充床反应器分别只能运行45天、40天和60天。因此,将假单胞菌属菌株NGK1的细胞固定在聚氨酯泡沫中比固定在其他测试基质中能实现更高效的萘降解。