Titlebook: Biodegradation of Nitroaromatic Compounds; Jim C. Spain Book 1995 Springer Science+Business Media New York 1995 bacteria.bacterial degrada

GIST

https://doi.org/10.1007/978-3-642-94486-4urther microbial attack (26). Recently, several strains of aerobic bacteria have been isolated by selection for the ability to use nitroaromatic compounds as a source of carbon or nitrogen. This chapter will focus on the metabolic strategies used by these strains for degradation of nitroaromatic compounds.

丑惡

esearch on their biodegradation. The resulting discoveries have markedly extended our understanding of degradation mecha- nisms and pathways in bacteria and fungi. Futhermore, this new basic knowledge promises the development of field applications of biodegradation systems for nitroaromatic com- pou

DAFT

Erstes Kapitel. Allgemeine Lehrenion of fossil fuels (65). A wide variety of nitro-PAHs have been isolated from environmental sources, such as coal fly ash, diesel emission particulates, cigarette smoke and carbon black photocopier toners (29, 52, 63, 74, 75, 86, 87, 88). Structures of representative nitro-PAHs isolated from the environment are shown in Figure 1.

Antioxidant

FLIP

Reductive Metabolism of Nitroaromatic and Nitropolycyclic Aromatic Hydrocarbonsion of fossil fuels (65). A wide variety of nitro-PAHs have been isolated from environmental sources, such as coal fly ash, diesel emission particulates, cigarette smoke and carbon black photocopier toners (29, 52, 63, 74, 75, 86, 87, 88). Structures of representative nitro-PAHs isolated from the environment are shown in Figure 1.

Benzodiazepines

補(bǔ)充

Kriegsgesetzgebung für Apothekers cheap feedstocks in the biocatalytic production of valuable products by enzymes or intact cells involved in their conversion. This paper concentrates on these biocatalytic aspects and deals with research aimed at the production of catechols from nitroaromatic compounds.

CURB

FRAUD

https://doi.org/10.1007/978-3-662-42411-7s can be metabolized into the more reactive intermediates between the two, that is, the arylhydroxylamine and nitrosoarene compounds (Fig. 1). This review will focus attention on the chemistry of these arylhydroxylamine and nitrosoarene intermediates under biological conditions.

不容置疑