Yen K M, Karl M R
Amgen Inc., Amgen Center, Thousand Oaks, California 91320-1789.
J Bacteriol. 1992 Nov;174(22):7253-61. doi: 10.1128/jb.174.22.7253-7261.1992.
Five genes, tmoABCDE, encoding toluene-4-monooxygenase (T4MO) were previously mapped to a 3.6-kb region of a 10.2-kb SacI DNA fragment isolated from Pseudomonas mendocina KR1 (K.-M. Yen, M. R. Karl, L. M. Blatt, M. J. Simon, R. B. Winter, P. R. Fausset, H. S. Lu, A. A. Harcourt, and K. K. Chen, J. Bacteriol. 173:5315-5327, 1991). In this report, we describe the identification and characterization of a DNA region in the SacI fragment whose expression enhances the T4MO activity determined by the tmoABCDE gene cluster. This region was mapped immediately downstream of the putative transcription termination sequence previously located at the end of the tmoABCDE gene cluster (Yen et al., J. Bacteriol., 1991) and was found to stimulate T4MO activity two- to threefold when expressed in Escherichia coli or Pseudomonas putida. Determination of the nucleotide sequence of this region revealed an open reading frame (ORF) of 978 bp. Expression of the ORF resulted in the synthesis of an approximately 37-kDa polypeptide whose N-terminal amino acid sequence completely matched that of the product predicted from the ORF. The ORF thus defines a gene, which has now been designated tmoF. The TmoF protein shares amino acid sequence homology with the reductases of several mono- and dioxygenase systems. In addition, the reductase component of the naphthalene dioxygenase system, encoded by the nahAa gene of plasmid NAH7 from P. putida G7, could largely replace the TmoF protein in stimulating T4MO activity, and TmoF could partially replace the NahAa protein in forming active naphthalene dioxygenase. The overall properties of tmoF suggest that it is a member of the T4mo gene cluster and encodes the NADH:ferredoxin oxidoreductase of the T4MO system.
之前已将编码甲苯-4-单加氧酶(T4MO)的五个基因tmoABCDE定位到从门多萨假单胞菌KR1分离出的10.2 kb SacI DNA片段的3.6 kb区域(K.-M. Yen、M. R. Karl、L. M. Blatt、M. J. Simon、R. B. Winter、P. R. Fausset、H. S. Lu、A. A. Harcourt和K. K. Chen,《细菌学杂志》173:5315 - 5327,1991年)。在本报告中,我们描述了SacI片段中一个DNA区域的鉴定和特性,该区域的表达增强了由tmoABCDE基因簇决定的T4MO活性。该区域位于先前位于tmoABCDE基因簇末端的假定转录终止序列的紧邻下游(Yen等人,《细菌学杂志》,1991年),并且当在大肠杆菌或恶臭假单胞菌中表达时,发现其能将T4MO活性提高两到三倍。对该区域核苷酸序列进行测定,揭示了一个978 bp的开放阅读框(ORF)。该ORF的表达导致合成了一种约37 kDa的多肽,其N端氨基酸序列与从该ORF预测的产物完全匹配。因此,该ORF定义了一个基因,现已命名为tmoF。TmoF蛋白与几种单加氧酶和双加氧酶系统的还原酶具有氨基酸序列同源性。此外,恶臭假单胞菌G7的质粒NAH7的nahAa基因编码的萘双加氧酶系统的还原酶成分,在刺激T4MO活性方面可在很大程度上替代TmoF蛋白,并且TmoF可在形成活性萘双加氧酶方面部分替代NahAa蛋白。tmoF的总体特性表明它是T4mo基因簇的一个成员,并编码T4MO系统的NADH:铁氧化还原蛋白氧化还原酶。