Hori K, Yamamoto Y, Tokita K, Saito F, Kurotsu T, Kanda M, Okamura K, Furuyama J, Saito Y
Department of Biochemistry, Hyogo College of Medicine.
J Biochem. 1991 Jul;110(1):111-9. doi: 10.1093/oxfordjournals.jbchem.a123528.
A fragment encoding proline-activating domain (grs 2-pro) of gramicidin S synthetase 2 (GS 2) was found in an 8.1-kilobase pairs (kb) DNA fragment of Bacillus brevis Nagano, which contained the full length of GS 1 gene (grs 1). The clones designated GS719 and GS708, which expressed gramicidin S synthetase 1, were elucidated to express immunoreactive proteins to GS 2 antibodies with approximate molecular weights of 115,000, 105,000 (GS719), and 110,000 (GS708). The partial purification of the gene products of these clones was carried out using DEAE-Sepharose CL-6B column chromatography. The immunoreactive proteins to GS 2 antibodies were separated from gramicidin S synthetase 1 protein and had specific proline-dependent ATP-32PPi exchange activity. The nucleotide sequence for the proline-activating domain in the 8.1-kb insert was determined. This fragment was 2,879 base pairs long, and encoded 959 amino acids. The calculated molecular weight of 111,671 was consistent with the apparent molecular weight of 115,000 found in SDS-PAGE of the immunoreactive products to GS 2 antibodies. The open reading frame for this protein followed grs 1 gene, though two were separated by a 73-base pair noncoding sequence, and remained open to the end.(ABSTRACT TRUNCATED AT 250 WORDS)
在短短芽孢杆菌长野株的一个8.1千碱基对(kb)的DNA片段中发现了编码短杆菌肽S合成酶2(GS 2)脯氨酸激活结构域(grs 2-pro)的一个片段,该片段包含GS 1基因(grs 1)的全长。已阐明命名为GS719和GS708的克隆表达短杆菌肽S合成酶1,它们还表达与GS 2抗体发生免疫反应的蛋白质,其近似分子量分别为115,000、105,000(GS719)和110,000(GS708)。使用DEAE-琼脂糖CL-6B柱色谱法对这些克隆的基因产物进行了部分纯化。与GS 2抗体发生免疫反应的蛋白质与短杆菌肽S合成酶1蛋白分离,并具有特定的脯氨酸依赖性ATP-32PPi交换活性。测定了8.1 kb插入片段中脯氨酸激活结构域的核苷酸序列。该片段长2879个碱基对,编码959个氨基酸。计算得到的分子量111,671与在GS 2抗体免疫反应产物的SDS-PAGE中发现的115,000的表观分子量一致。该蛋白的开放阅读框紧跟在grs 1基因之后,尽管两者被一个73个碱基对的非编码序列隔开,并且一直开放到末端。(摘要截短至250字)