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Title: Use of a genetically engineered Escherichia coli strain to produce 1,2-dihydroxy-4 prime -chlorobiphenyl

Journal Article · · Applied and Environmental Microbiology; (United States)
OSTI ID:7114693
;  [1]
  1. Oakland Univ., Rochester, MI (United States)

Genetically engineered kanamycin-resistant Escherichia coli HB101 containing the mutant chimeric plasmid pAW6194-T17 specifying biphenyl dioxygenase and dihydrodiol dehydrogenase and lacking the ability to produce active 3-phenylcatechol dioxygenase was used to produce 1,2-dihydroxy-4{prime}-chlorobiphenyl (DHCB) from 4-chlorobiphenyl produced 110 {mu}M DHCB. The K{sub m} for 4-chlorobiphenyl was 3.3 mM. Biotransformation of DHCB from 4-chlorobiphenyl was maximum when cells (2.5 mg of protein per ml) were incubated with shaking (150 rpm) at pH 7.0 and 30C for 6 h. The enzymatically produced DHCB was a suitable substrate for assaying 3-phenylcatechol dioxygenase activity. Biologically produced DHCB showed UV and mass spectra similar to those of chemically synthesized DHCB. The bioconversion rate of ortho-substituted chlorobiphenyl was slower than that of the para- or meta-substituted chlorobiphenyl.

OSTI ID:
7114693
Journal Information:
Applied and Environmental Microbiology; (United States), Vol. 58:4; ISSN 0099-2240
Country of Publication:
United States
Language:
English