Shim H, Chauhan S, Ryoo D, Bowers K, Thomas S M, Canada K A, Burken J G, Wood T K
Department of Chemical Engineering, University of Connecticut, Storrs, Connecticut 06269-3222, USA.
Appl Environ Microbiol. 2000 Nov;66(11):4673-8. doi: 10.1128/AEM.66.11.4673-4678.2000.
Indigenous bacteria from poplar tree (Populus canadensis var. eugenei 'Imperial Carolina') and southern California shrub rhizospheres, as well as two tree-colonizing Rhizobium strains (ATCC 10320 and ATCC 35645), were engineered to express constitutively and stably toluene o-monooxygenase (TOM) from Burkholderia cepacia G4 by integrating the tom locus into the chromosome. The poplar and Rhizobium recombinant bacteria degraded trichloroethylene at a rate of 0.8 to 2.1 nmol/min/mg of protein and were competitive against the unengineered hosts in wheat and barley rhizospheres for 1 month (colonization occurred at a level of 1.0 x 10(5) to 23 x 10(5) CFU/cm of root). In addition, six of these recombinants colonized poplar roots stably and competitively with populations as large as 79% +/- 12% of all rhizosphere bacteria after 28 days (0.2 x 10(5) to 31 x 10(5) CFU/cm of root). Furthermore, five of the most competitive poplar recombinants (e.g., Pb3-1 and Pb5-1, which were identified as Pseudomonas sp. strain PsK recombinants) retained the ability to express TOM for 29 days as 100% +/- 0% of the recombinants detected in the poplar rhizosphere expressed TOM constitutively.
通过将来自洋葱伯克霍尔德氏菌G4的甲苯邻单加氧酶(TOM)基因座整合到染色体中,对来自加拿大杨(Populus canadensis var. eugenei 'Imperial Carolina')和南加州灌木根际的本土细菌,以及两种定殖于树木的根瘤菌菌株(ATCC 10320和ATCC 35645)进行基因工程改造,使其组成型且稳定地表达TOM。杨树和根瘤菌重组细菌以0.8至2.1 nmol/分钟/毫克蛋白质的速率降解三氯乙烯,并且在小麦和大麦根际中与未改造的宿主竞争达1个月(定殖水平为1.0×10⁵至23×10⁵ CFU/厘米根)。此外,其中六种重组菌在28天后稳定且竞争性地定殖于杨树根,其数量高达根际所有细菌的79%±12%(0.2×10⁵至31×10⁵ CFU/厘米根)。此外,五个竞争力最强的杨树重组菌(例如,被鉴定为假单胞菌属菌株PsK重组菌的Pb3-1和Pb5-1)能够持续29天表达TOM,因为在杨树根际检测到的重组菌中有100%±0%组成型表达TOM。