Black S M, Ortiz de Montellano P R
Department of Pharmaceutical Chemistry, School of Pharmacy, University of California, San Francisco 94143-0446, USA.
DNA Cell Biol. 1995 Sep;14(9):789-94. doi: 10.1089/dna.1995.14.789.
A cDNA encoding rat neuronal nitric oxide synthase (nNOS) was cloned into the yeast expression vector pMA56 to generate pA379. Transformation of Saccharomyces cerevisiae strain BJ2168 with this plasmid resulted in the synthesis of nNOS at levels of 0.5-1.0 mg/liter. The protein is localized in the cytosol and is catalytically active as determined by the conversion of [3H]-L-arginine to [3H]-L-citrulline and NO. The enzyme was purified by calmodulin-Sepharose affinity chromatography and its catalytic activity was found to be both calcium and calmodulin dependent. Overexpression of nNOS in S. cerevisiae and purification of the recombinant protein will facilitate detailed characterization of this important enzyme.
将编码大鼠神经元型一氧化氮合酶(nNOS)的cDNA克隆到酵母表达载体pMA56中,构建成pA379。用该质粒转化酿酒酵母菌株BJ2168,可合成水平为0.5 - 1.0毫克/升的nNOS。该蛋白定位于细胞质中,通过将[3H]-L-精氨酸转化为[3H]-L-瓜氨酸和一氧化氮来确定其具有催化活性。通过钙调蛋白-琼脂糖亲和层析法纯化该酶,发现其催化活性依赖于钙和钙调蛋白。在酿酒酵母中过表达nNOS并纯化重组蛋白将有助于对这种重要酶进行详细表征。