Yang Kyung Seok, Sohn Jung-Hoon, Kim Hyung Kwoun
Department of Biotechnology, Catholic University of Korea, Bucheon 420-743, Republic of Korea.
J Biosci Bioeng. 2009 Jun;107(6):599-604. doi: 10.1016/j.jbiosc.2009.01.009.
Biodiesel, an alternative fuel, is generated via the transesterification reaction of vegetable oil or animal oil with alcohol. Currently, many reports have noted that microbial lipases might be utilized for the production of biodiesel. Among them, immobilized Candida antarctica lipase B (Novozym435) is frequently utilized for its biocatalytic efficiency and availability. However, as the enzyme is unstable in a medium containing high concentrations of methanol, a multi-stepwise methanol supply is required for the efficient production of biodiesel. Photobacterium lipolyticum lipase (M37) was determined to be quite stable in a medium containing a high concentration of methanol. The enzyme activity was maintained for longer than 48 h without any loss at a methanol concentration of 10%. In an effort to evaluate enzyme performance in the production of biodiesel, we have compared M37 lipase and Novozym435 in the biodiesel production reaction using fresh or waste oil and methanol. In the 3-stepwise methanol feeding method generally conducted for Novozym435 in biodiesel production, the M37 lipase showed a similar or superior conversion yield to Novozym435. However, the M37 lipase evidenced significantly higher conversion yields in the 2 and 1 step methanol feeding reactions. Particularly in the 1 step process using 10% of methanol where almost no conversion was detected by Novozym435, the biodiesel yield achieved with M37 lipase reached a level of up to 70% of the possible maximum yield. Consequently, this methanol-tolerant lipase, M37, has been shown to be a suitable enzyme for use in the biodiesel production process.
生物柴油作为一种替代燃料,是通过植物油或动物油与醇的酯交换反应生成的。目前,许多报道指出微生物脂肪酶可用于生物柴油的生产。其中,固定化南极假丝酵母脂肪酶B(诺维信435)因其生物催化效率和可得性而被频繁使用。然而,由于该酶在高浓度甲醇的介质中不稳定,因此高效生产生物柴油需要多步供应甲醇。已确定解脂发光杆菌脂肪酶(M37)在含有高浓度甲醇的介质中相当稳定。在甲醇浓度为10%时,酶活性可维持超过48小时且无任何损失。为了评估该酶在生物柴油生产中的性能,我们在使用新鲜油或废油与甲醇的生物柴油生产反应中比较了M37脂肪酶和诺维信435。在生物柴油生产中通常用于诺维信435的三步甲醇进料方法中,M37脂肪酶的转化率与诺维信435相似或更高。然而,M37脂肪酶在两步和一步甲醇进料反应中的转化率明显更高。特别是在使用10%甲醇的一步法中,诺维信435几乎检测不到转化,而M37脂肪酶实现的生物柴油产量达到了可能最大产量的70%。因此,这种耐甲醇脂肪酶M37已被证明是生物柴油生产过程中适用的酶。