Kobayashi M, Izui H, Nagasawa T, Yamada H
Department of Agricultural Chemistry, Faculty of Agriculture, Kyoto University, Japan.
Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):247-51. doi: 10.1073/pnas.90.1.247.
Indole-3-acetic acid is the major auxin in most plants. In Cruciferae, including Brassicaceae, indole-3-acetic acid is synthesized from indole-3-acetonitrile by nitrilase, after indole-3-acetonitrile is formed from tryptophan via indole-3-acetaldoxime or indole glycosinolates as the intermediate. We cloned and sequenced the gene for nitrilase (EC 3.5.5.1), which catalyzes the hydrolysis of indole-3-acetonitrile to indole-3-acetic acid, from Alcaligenes faecalis JM3. The amino acid sequence deduced from the nucleotide sequence of the nitrilase gene shows 34.7% identity with that of Klebsiella ozaenae nitrilase. A DNA clone containing the nitrilase gene expressed the active enzyme in Escherichia coli with excellent yield. Among five cysteine residues (Cys-40, Cys-115, Cys-162, Cys-163, and Cys-218) in the Alcaligenes nitrilase, only Cys-163 was conserved at the corresponding position in the Klebsiella nitrilase. Two mutant enzymes, in which Cys-162 and Cys-163 were replaced with Asn and Ala, respectively, were constructed by site-directed mutagenesis. A 35% increase of the specific activity and a large reduction of the Km for thiophene-2-acetonitrile (which was used as a standard substrate for the nitrilase) were observed in the Cys-162-->Asn mutant enzyme. The Cys-163-->Ala mutation resulted in complete loss of nitrilase activity, clearly indicating that Cys-163 is crucial for the activity and Cys-162 could not provide the catalytic function of Cys-163.
吲哚 - 3 - 乙酸是大多数植物中的主要生长素。在十字花科植物(包括芸苔科)中,吲哚 - 3 - 乙酸是由腈水解酶将吲哚 - 3 - 乙腈水解而成,吲哚 - 3 - 乙腈是由色氨酸经吲哚 - 3 - 乙醛肟或吲哚硫苷作为中间体形成的。我们从粪产碱菌JM3中克隆并测序了腈水解酶(EC 3.5.5.1)的基因,该酶催化吲哚 - 3 - 乙腈水解为吲哚 - 3 - 乙酸。从腈水解酶基因的核苷酸序列推导的氨基酸序列与肺炎克雷伯菌腈水解酶的氨基酸序列具有34.7%的同一性。一个含有腈水解酶基因的DNA克隆在大肠杆菌中表达了活性酶,产量很高。在产碱菌腈水解酶的五个半胱氨酸残基(Cys - 40、Cys - 115、Cys - 162、Cys - 163和Cys - 218)中,只有Cys - 163在肺炎克雷伯菌腈水解酶的相应位置保守。通过定点诱变构建了两个突变酶,其中Cys - 162和Cys - 163分别被Asn和Ala取代。在Cys - 162→Asn突变酶中,观察到比活性增加了35%,并且用作腈水解酶标准底物的噻吩 - 2 - 乙腈的Km大幅降低。Cys - 163→Ala突变导致腈水解酶活性完全丧失,清楚地表明Cys - 163对活性至关重要,而Cys - 162不能提供Cys - 163的催化功能。