Pasti-Grigsby M B, Paszczynski A, Goszczynski S, Crawford D L, Crawford R L
Department of Bacteriology and Biochemistry, College of Agriculture, University of Idaho, Moscow 83843.
Appl Environ Microbiol. 1992 Nov;58(11):3605-13. doi: 10.1128/aem.58.11.3605-3613.1992.
Twenty-two azo dyes were used to study the influence of substituents on azo dye biodegradability and to explore the possibility of enhancing the biodegradabilities of azo dyes without affecting their properties as dyes by changing their chemical structures. Streptomyces spp. and Phanerochaete chrysosporium were used in the study. None of the actinomycetes (Streptomyces rochei A10, Streptomyces chromofuscus A11, Streptomyces diastaticus A12, S. diastaticus A13, and S. rochei A14) degraded the commercially available Acid Yellow 9. Decolorization of monosulfonated mono azo dye derivatives of azobenzene by the Streptomyces spp. was observed with five azo dyes having the common structural pattern of a hydroxy group in the para position relative to the azo linkage and at least one methoxy and/or one alkyl group in an ortho position relative to the hydroxy group. The fungus P. chrysosporium attacked Acid Yellow 9 to some extent and extensively decolorized several azo dyes. A different pattern was seen for three mono azo dye derivatives of naphthol. Streptomyces spp. decolorized Orange I but not Acid Orange 12 or Orange II. P. chrysosporium, though able to transform these three azo dyes, decolorized Acid Orange 12 and Orange II more effectively than Orange I. A correlation was observed between the rate of decolorization of dyes by Streptomyces spp. and the rate of oxidative decolorization of dyes by a commercial preparation of horseradish peroxidase type II, extracellular peroxidase preparations of S. chromofuscus A11, or Mn(II) peroxidase from P. chrysosporium. Ligninase of P. chrysosporium showed a dye specificity different from that of the other oxidative enzymes.(ABSTRACT TRUNCATED AT 250 WORDS)
使用22种偶氮染料来研究取代基对偶氮染料生物降解性的影响,并探索通过改变化学结构来提高偶氮染料生物降解性而又不影响其染料性能的可能性。研究中使用了链霉菌属和黄孢原毛平革菌。没有一种放线菌(罗氏链霉菌A10、暗产色链霉菌A11、淀粉酶链霉菌A12、淀粉酶链霉菌A13和罗氏链霉菌A14)能降解市售的酸性黄9。链霉菌属对单磺酸化单偶氮苯染料衍生物进行脱色,观察到5种偶氮染料具有相对于偶氮键在对位有羟基且相对于羟基在邻位至少有一个甲氧基和/或一个烷基的共同结构模式。真菌黄孢原毛平革菌在一定程度上能降解酸性黄9,并能使几种偶氮染料大量脱色。萘酚的三种单偶氮染料衍生物呈现出不同的脱色模式。链霉菌属能使橙黄Ⅰ脱色,但不能使酸性橙12或橙黄Ⅱ脱色。黄孢原毛平革菌虽然能够转化这三种偶氮染料,但对酸性橙12和橙黄Ⅱ的脱色效果比对橙黄Ⅰ更有效。观察到链霉菌属对染料的脱色速率与市售Ⅱ型辣根过氧化物酶、暗产色链霉菌A11的细胞外过氧化物酶制剂或黄孢原毛平革菌的锰(Ⅱ)过氧化物酶对染料的氧化脱色速率之间存在相关性。黄孢原毛平革菌的木质素酶显示出与其他氧化酶不同的染料特异性。(摘要截短于250字)