» Articles » PMID: 1480115

Molecular Mechanisms of Genetic Adaptation to Xenobiotic Compounds

Overview
Journal Microbiol Rev
Specialty Microbiology
Date 1992 Dec 1
PMID 1480115
Citations 147
Authors
Affiliations
Soon will be listed here.
Abstract

Microorganisms in the environment can often adapt to use xenobiotic chemicals as novel growth and energy substrates. Specialized enzyme systems and metabolic pathways for the degradation of man-made compounds such as chlorobiphenyls and chlorobenzenes have been found in microorganisms isolated from geographically separated areas of the world. The genetic characterization of an increasing number of aerobic pathways for degradation of (substituted) aromatic compounds in different bacteria has made it possible to compare the similarities in genetic organization and in sequence which exist between genes and proteins of these specialized catabolic routes and more common pathways. These data suggest that discrete modules containing clusters of genes have been combined in different ways in the various catabolic pathways. Sequence information further suggests divergence of catabolic genes coding for specialized enzymes in the degradation of xenobiotic chemicals. An important question will be to find whether these specialized enzymes evolved from more common isozymes only after the introduction of xenobiotic chemicals into the environment. Evidence is presented that a range of genetic mechanisms, such as gene transfer, mutational drift, and genetic recombination and transposition, can accelerate the evolution of catabolic pathways in bacteria. However, there is virtually no information concerning the rates at which these mechanisms are operating in bacteria living in nature and the response of such rates to the presence of potential (xenobiotic) substrates. Quantitative data on the genetic processes in the natural environment and on the effect of environmental parameters on the rate of evolution are needed.

Citing Articles

Comparative genomics based exploration of xenobiotic degradation patterns in , , and isolated from diverse ecological habitats.

Ghimire N, Kim B, Han S, Oh T Heliyon. 2024; 10(22):e40280.

PMID: 39584100 PMC: 11585801. DOI: 10.1016/j.heliyon.2024.e40280.


The Domestication of Wild Boar Could Result in a Relaxed Selection for Maintaining Olfactory Capacity.

Buglione M, Rivieccio E, Aceto S, Paturzo V, Biondi C, Fulgione D Life (Basel). 2024; 14(8).

PMID: 39202786 PMC: 11355481. DOI: 10.3390/life14081045.


Discovery of the 1-naphthylamine biodegradation pathway reveals a broad-substrate-spectrum enzyme catalyzing 1-naphthylamine glutamylation.

Zhang S, Deng S, Li T, Maloney M, Li D, Spain J Elife. 2024; 13.

PMID: 39163210 PMC: 11335346. DOI: 10.7554/eLife.95555.


Insights into the genomic and functional divergence of NAT gene family to serve microbial secondary metabolism.

Boukouvala S, Kontomina E, Olbasalis I, Patriarcheas D, Tzimotoudis D, Arvaniti K Sci Rep. 2024; 14(1):14905.

PMID: 38942826 PMC: 11213898. DOI: 10.1038/s41598-024-65342-4.


Whole genome analyses of toxicants tolerance genes of Apis mellifera gut-derived Enterococcus faecium strains.

Zaghloul H, El Halfawy N BMC Genomics. 2023; 24(1):479.

PMID: 37620768 PMC: 10463970. DOI: 10.1186/s12864-023-09590-0.


References
1.
Chatfield L, Williams P . Naturally occurring TOL plasmids in Pseudomonas strains carry either two homologous or two nonhomologous catechol 2,3-oxygenase genes. J Bacteriol. 1986; 168(2):878-85. PMC: 213566. DOI: 10.1128/jb.168.2.878-885.1986. View

2.
Reynolds A, Felton J, Wright A . Insertion of DNA activates the cryptic bgl operon in E. coli K12. Nature. 1981; 293(5834):625-9. DOI: 10.1038/293625a0. View

3.
Bej A, Steffan R, DiCesare J, Haff L, Atlas R . Detection of coliform bacteria in water by polymerase chain reaction and gene probes. Appl Environ Microbiol. 1990; 56(2):307-14. PMC: 183336. DOI: 10.1128/aem.56.2.307-314.1990. View

4.
Chakrabarty A, Friello D, Bopp L . Transposition of plasmid DNA segments specifying hydrocarbon degradation and their expression in various microorganisms. Proc Natl Acad Sci U S A. 1978; 75(7):3109-12. PMC: 392723. DOI: 10.1073/pnas.75.7.3109. View

5.
NEIDLE E, Hartnett C, ORNSTON L, Bairoch A, Rekik M, Harayama S . cis-diol dehydrogenases encoded by the TOL pWW0 plasmid xylL gene and the Acinetobacter calcoaceticus chromosomal benD gene are members of the short-chain alcohol dehydrogenase superfamily. Eur J Biochem. 1992; 204(1):113-20. DOI: 10.1111/j.1432-1033.1992.tb16612.x. View