{"title":"5-Aminolevulinic Acid: Production by Fermentation, and Agricultural and Biomedical Applications","authors":"S. Nishikawa, Y. Murooka","doi":"10.1080/02648725.2001.10648012","DOIUrl":null,"url":null,"abstract":"5-Alninolevulinic acid (ALA) is kno\\vn as a C0l11ffiOIl precursor of tetrapyrrole C0111pounds (e.g. chlorophyll, henle and vitamin Bl~) in all living organisJns (Figure 7. I). ALA has the potential to be widely used as a biodegradable herbicide (Rebeiz et al., 1984), insecticide (Rebeiz et ai., 1988), and in photodynanlic cancer therapy (Kennedy el al., 1990). Recently, Hotta et al. (1997) have reported that a low level of ALA stitnulates plant growth and increases the yields of several crops. ALA also has potential for LIse as an active substrate for the chemical synthesis of nlaterials. For these reasons, a nunlber of ALA production nlethods have been developed. ALA has been synthesized chenlically via selective reduction of acyl cyanides (Pfaltz and An\\var~ 1984) or via dye-sensitized oxygenation ofN-furfurylphthalilnide (Takeya et al., 1989) (Figure 7.2). However, the chenlical synthesis of ALA requires at least four reaction steps and the yield is less than 60%. The high cost ofproductlon of ALA has thus far limited its cOlunlcrcia) utilization. Microorganisills such as Clostridhl111 thernlO{lCeticul1l (Koesnandar et al., 1989), methanogens (Lin et al., 1989), Chlorella spp. (Sasaki et al., 1995: Ano et al., 1999, 20(0). and photosynthetic bacteria (van der Mariet and Zeikus., ]996; Sasaki et al., 1989, 1990, 1993., 1995; Tanaka el al., 1991, 1994a,b) produce ALA in considerable anlounts. The ALA production by photosynthetic bacteria, ho\\vever, requires light illll1nination and has been found to be sensitive to aeration. A crude extract froln","PeriodicalId":8931,"journal":{"name":"Biotechnology and Genetic Engineering Reviews","volume":"7 1","pages":"149 - 170"},"PeriodicalIF":0.0000,"publicationDate":"2001-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and Genetic Engineering Reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/02648725.2001.10648012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20
Abstract
5-Alninolevulinic acid (ALA) is kno\vn as a C0l11ffiOIl precursor of tetrapyrrole C0111pounds (e.g. chlorophyll, henle and vitamin Bl~) in all living organisJns (Figure 7. I). ALA has the potential to be widely used as a biodegradable herbicide (Rebeiz et al., 1984), insecticide (Rebeiz et ai., 1988), and in photodynanlic cancer therapy (Kennedy el al., 1990). Recently, Hotta et al. (1997) have reported that a low level of ALA stitnulates plant growth and increases the yields of several crops. ALA also has potential for LIse as an active substrate for the chemical synthesis of nlaterials. For these reasons, a nunlber of ALA production nlethods have been developed. ALA has been synthesized chenlically via selective reduction of acyl cyanides (Pfaltz and An\var~ 1984) or via dye-sensitized oxygenation ofN-furfurylphthalilnide (Takeya et al., 1989) (Figure 7.2). However, the chenlical synthesis of ALA requires at least four reaction steps and the yield is less than 60%. The high cost ofproductlon of ALA has thus far limited its cOlunlcrcia) utilization. Microorganisills such as Clostridhl111 thernlO{lCeticul1l (Koesnandar et al., 1989), methanogens (Lin et al., 1989), Chlorella spp. (Sasaki et al., 1995: Ano et al., 1999, 20(0). and photosynthetic bacteria (van der Mariet and Zeikus., ]996; Sasaki et al., 1989, 1990, 1993., 1995; Tanaka el al., 1991, 1994a,b) produce ALA in considerable anlounts. The ALA production by photosynthetic bacteria, ho\vever, requires light illll1nination and has been found to be sensitive to aeration. A crude extract froln
5-丙烯乙酰丙酸(ALA)在所有生物体中都是四吡啶(如叶绿素、汞和维生素Bl~)的前体(图7)。I). ALA作为可生物降解除草剂(Rebeiz et al., 1984)、杀虫剂(Rebeiz et ai., 1984)具有广泛应用的潜力。, 1988),以及光动力癌症治疗(Kennedy等,1990)。最近,Hotta等人(1997)报道了低水平的ALA能促进植物生长并提高几种作物的产量。ALA也有潜力作为LIse的活性底物用于非材料的化学合成。由于这些原因,已经开发了许多ALA生产方法。ALA的化学合成是通过酰基氰化物的选择性还原(Pfaltz和An\var~ 1984)或n -呋喃基酞胺的染料敏化氧化(Takeya et al., 1989)(图7.2)。然而,ALA的化学合成至少需要四个反应步骤,收率低于60%。目前,ALA的高生产成本限制了其在国内的应用。微生物如梭状芽孢杆菌(Koesnandar et al., 1989)、产甲烷菌(Lin et al., 1989)、小球藻(Sasaki et al., 1995; Ano et al., 1999, 20)。以及光合细菌(van der Mariet和Zeikus)。, 996;Sasaki et al., 1989,1990,1993。, 1995;Tanaka等人,1991,1994a,b)在相当大的范围内产生ALA。然而,光合细菌生产ALA需要光照,并且对曝气很敏感。一种粗提取物