DAVIS J B, RAYMOND R L
Appl Microbiol. 1961 Sep;9(5):383-8. doi: 10.1128/am.9.5.383-388.1961.
Nocardia 107-332, a soil isolate, oxidizes short-chain alkyl-substituted cyclic hydrocarbons to cyclic acids while growing on n-alkanes. Cyclic acids are produced also from relatively long-chain alkyl-substituted cyclics such as n-nonylbenzene or n-dodecylbenzene which alone support growth in a mineral-salts medium. omega-Oxidation of the alkyl substituents is followed by beta-oxidation. It is of particular interest that cyclic acids such as cyclohexaneacetic and phenylacetic with C(2) residual carboxylic acid substituents are resistant to further oxidation by the nocardia but cyclic acids with C(1) or C(3) substituents are readily oxidized and utilized for growth. The specificity of microbial oxidations is demonstrated by the conversion of p-isopropyltoluene (p-cymene) to p-isopropylbenzoic acid in n-alkane, growth-supported nocardia cultures.
诺卡氏菌107 - 332是一种从土壤中分离出的菌株,它在以正构烷烃为生长底物时,能将短链烷基取代的环烃氧化为环酸。相对长链的烷基取代环烃,如正壬基苯或正十二烷基苯,在仅以其作为生长底物的无机盐培养基中,也能产生环酸。烷基取代基先发生ω-氧化,随后进行β-氧化。特别值得关注的是,具有C(2)残留羧酸取代基的环酸,如环己烷乙酸和苯乙酸,对诺卡氏菌的进一步氧化具有抗性,但具有C(1)或C(3)取代基的环酸则很容易被氧化并用于生长。在以正构烷烃为生长底物的诺卡氏菌培养物中,对异丙基甲苯(对异丙基苯)转化为对异丙基苯甲酸,证明了微生物氧化的特异性。