Rolland N, Droux M, Lebrun M, Douce R
Unité Mixte CNRS/Rhône-Poulenc, Unité Associée au Centre National de la Recherche Scientifique, UMR 41, Lyon, France.
Arch Biochem Biophys. 1993 Jan;300(1):213-22. doi: 10.1006/abbi.1993.1030.
The last enzymatic step for L-cysteine biosynthesis is catalyzed by O-acetylserine(thiol)lyase (OASTL, EC 4.2.99.8) which synthesizes L-cysteine from O-acetylserine and "sulfide." We have isolated and characterized a full-length cDNA (1432 bp) from a lambda gt11 library of spinach leaf encoding the complete precursor of the chloroplast isoform. The 1149-nucleotide open reading frame coding for O-acetylserine(thiol)lyase was in the direction opposite that of the lambda gt11 beta-galactosidase gene. The derived amino acid sequence indicates that the protein precursor consists of 383 amino acid residues including a N-terminal presequence peptide of 52 residues. The amino acid sequence of mature spinach chloroplast O-acetylserine(thiol)lyase shows 40 and 57% homology with its bacterial counterparts. Sequence comparison with several pyridoxal 5'-phosphate-containing proteins reveals the presence of a lysine residue assumed to be involved in cofactor binding. A synthetic cDNA was constructed, coding for the entire 331-amino-acid mature O-acetylserine(thiol)lyase and for an initiating methionine. A high level of expression of the active mature chloroplast isoform was achieved in an Escherichia coli strain carrying the T7 RNA polymerase system (F. W. Studier, A. H. Rosenberg, J. J. Dunn, and J. W. Dubendorff, 1990, in Methods in Enzymology, D. V. Goeddel, Ed., Vol. 185, pp. 60-89, Academic Press, San Diego, CA). Addition of pyridoxine to the bacterial growth medium enhanced the enzyme activity due to the recombinant protein. The extent of production is 25-fold higher than in chloroplast from spinach leaves and the recombinant protein presents the relative molecular mass and immunological properties of the natural enzyme from spinach leaf chloroplast. This work, together with our previous biochemical studies, are in accordance with a prokaryotic type enzyme for L-cysteine biosynthesis in higher plant chloroplasts. Southern blot analysis indicated that O-acetylserine(thiol)lyase is encoded by multiple genes in the spinach leaf genomic DNA.
L-半胱氨酸生物合成的最后一个酶促步骤由O-乙酰丝氨酸(硫醇)裂合酶(OASTL,EC 4.2.99.8)催化,该酶从O-乙酰丝氨酸和“硫化物”合成L-半胱氨酸。我们从菠菜叶的λgt11文库中分离并鉴定了一个全长cDNA(1432 bp),其编码叶绿体同工型的完整前体。编码O-乙酰丝氨酸(硫醇)裂合酶的1149个核苷酸的开放阅读框与λgt11β-半乳糖苷酶基因的方向相反。推导的氨基酸序列表明,蛋白质前体由383个氨基酸残基组成,包括一个52个残基的N端前序列肽。成熟菠菜叶绿体O-乙酰丝氨酸(硫醇)裂合酶的氨基酸序列与其细菌对应物显示出40%和57%的同源性。与几种含磷酸吡哆醛的蛋白质的序列比较揭示了一个假定参与辅因子结合的赖氨酸残基的存在。构建了一个合成cDNA,编码整个331个氨基酸的成熟O-乙酰丝氨酸(硫醇)裂合酶和一个起始甲硫氨酸。在携带T7 RNA聚合酶系统的大肠杆菌菌株中实现了活性成熟叶绿体同工型的高水平表达(F.W.Studier、A.H.Rosenberg、J.J.Dunn和J.W.Dubendorff,1990年,《酶学方法》,D.V.Goeddel编,第185卷,第60 - 89页,学术出版社,加利福尼亚州圣地亚哥)。向细菌生长培养基中添加吡哆醇可提高重组蛋白的酶活性。产量比菠菜叶叶绿体中的高25倍,重组蛋白呈现出菠菜叶叶绿体天然酶的相对分子质量和免疫特性。这项工作与我们之前的生化研究一致,表明高等植物叶绿体中L-半胱氨酸生物合成的酶是原核类型的。Southern印迹分析表明,O-乙酰丝氨酸(硫醇)裂合酶由菠菜叶基因组DNA中的多个基因编码。