Baur H, Luethi E, Stalon V, Mercenier A, Haas D
Mikrobiologisches Institut, Eidgenössische Technische Hochschule, Zürich, Switzerland.
Eur J Biochem. 1989 Jan 15;179(1):53-60. doi: 10.1111/j.1432-1033.1989.tb14520.x.
The arcABC operon of Pseudomonas aeruginosa encodes arginine deiminase, catabolic ornithine carbamoyltransferase and carbamate kinase, respectively. We have determined the nucleotide sequences of the arcA and arcC genes. The arcA open reading frame specifies a polypeptide of 46.3 kDa. The same molecular mass was obtained for the subunit of purified arginine deiminase after electrophoresis under denaturing conditions. The N-terminal amino acid sequence of arginine deiminase was in agreement with the corresponding nucleotide sequence. The native arginine deiminase had an estimated molecular mass of 175-180 kDa, suggesting a tetrametric structure. The enzyme was activated by Mg2+ or Mn2+ and strongly inhibited by Zn2+. The apparent Km for L-arginine was 0.04 mM in the presence of Mg2+ and 0.47 mM without Mg2+. The arcC open reading frame codes for a 33-kDa protein, confirming the molecular mass previously reported for the subunit of carbamate kinase. The translation-initiation site of arcC was determined by deletion mapping. Two regions of dyad symmetry found between arcA and arcC might stabilize the putative arcABC transcript in the upstream (arcA) region; this might contribute to the high level of arcA expression as compared to the moderate level of arcC expression. Carbamate kinase had 37% sequence similarity (and 13.5% identity) with the C-terminal part of carbamoyl-phosphate synthetase (large subunit) from Escherichia coli. Arginine deiminase had no apparent similarity with argininosuccinate lyase. Thus, the arcA and arcC genes do not appear to be closely related to arginine biosynthetic genes, whereas it had previously been shown that the arcB gene has a high degree of identity with the arginine biosynthetic argF genes of P. aeruginosa and E. coli.
铜绿假单胞菌的arcABC操纵子分别编码精氨酸脱亚氨酶、分解代谢型鸟氨酸氨甲酰基转移酶和氨基甲酸激酶。我们已经测定了arcA和arcC基因的核苷酸序列。arcA开放阅读框编码一个46.3 kDa的多肽。在变性条件下进行电泳后,纯化的精氨酸脱亚氨酶亚基获得了相同的分子量。精氨酸脱亚氨酶的N端氨基酸序列与相应的核苷酸序列一致。天然精氨酸脱亚氨酶的估计分子量为175 - 180 kDa,表明其为四聚体结构。该酶被Mg2+或Mn2+激活,并被Zn2+强烈抑制。在有Mg2+存在时,L - 精氨酸的表观Km为0.04 mM,无Mg2+时为0.47 mM。arcC开放阅读框编码一个33 kDa的蛋白质,证实了先前报道的氨基甲酸激酶亚基的分子量。arcC的翻译起始位点通过缺失图谱确定。在arcA和arcC之间发现的两个二元对称区域可能稳定上游(arcA)区域的假定arcABC转录本;与arcC表达的中等水平相比,这可能有助于arcA的高水平表达。氨基甲酸激酶与来自大肠杆菌的氨甲酰磷酸合成酶(大亚基)的C端部分具有37%的序列相似性(和13.5%的同一性)。精氨酸脱亚氨酶与精氨琥珀酸裂解酶没有明显相似性。因此,arcA和arcC基因似乎与精氨酸生物合成基因没有密切关系,而先前已经表明arcB基因与铜绿假单胞菌和大肠杆菌精氨酸生物合成的argF基因具有高度同一性。