首页> 外文期刊>Journal of bacteriology >Characterization of the Cephalosporium acremonium pcbAB gene encoding alpha-aminoadipyl-cysteinyl-valine synthetase, a large multidomain peptide synthetase: linkage to the pcbC gene as a cluster of early cephalosporin biosynthetic genes and evidence of multiple functional domains.
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Characterization of the Cephalosporium acremonium pcbAB gene encoding alpha-aminoadipyl-cysteinyl-valine synthetase, a large multidomain peptide synthetase: linkage to the pcbC gene as a cluster of early cephalosporin biosynthetic genes and evidence of multiple functional domains.

机译:头孢菌属顶头孢霉pcbAB基因的编码,该基因编码α-氨基己二酰基-半胱氨酸-缬氨酸合成酶,一种大型的多域肽合成酶:作为早期头孢菌素生物合成基因的簇和多个功能域的证据与pcbC基因连锁。

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A 24-kb region of Cephalosporium acremonium C10 DNA was cloned by hybridization with the pcbAB and pcbC genes of Penicillium chrysogenum. A 3.2-kb BamHI fragment of this region complemented the mutation in the structural pcbC gene of the C. acremonium N2 mutant, resulting in cephalosporin production. A functional alpha-aminoadipyl-cysteinyl-valine (ACV) synthetase was encoded by a 15.6-kb EcoRI-BamHI DNA fragment, as shown by complementation of an ACV synthetase-deficient mutant of P. chrysogenum. Two transcripts of 1.15 and 11.4 kb were found by Northern (RNA blot) hybridization with probes internal to the pcbC and pcbAB genes, respectively. An open reading frame of 11,136 bp was located upstream of the pcbC gene that matched the 11.4-kb transcript initiation and termination regions. It encoded a protein of 3,712 amino acids with a deduced Mr of 414,791. The nucleotide sequence of the gene showed 62.9% similarity to the pcbAB gene encoding the ACV synthetase of P. chrysogenum; 54.9% of the amino acids were identical in both ACV synthetases. Three highly repetitive regions occur in the deduced amino acid sequence of C. acremonium ACV synthetase. Each is similar to the three repetitive domains in the deduced sequence of P. chrysogenum ACV synthetase and also to the amino acid sequence of gramicidin synthetase I and tyrocidine synthetase I of Bacillus brevis. These regions probably correspond to amino acid activating domains in the ACV synthetase protein. In addition, a thioesterase domain was present in the ACV synthetases of both fungi. A similarity has been found between the domains existing in multienzyme nonribosomal peptide synthetases and polyketide and fatty acid synthetases. The pcbAB gene is linked to the pcbC gene, forming a cluster of early cephalosporin-biosynthetic genes.
机译:通过与产黄青霉的pcbAB和pcbC基因杂交,克隆了一个顶头孢霉C10 DNA的24 kb区域。该区域的3.2kb BamHI片段补充了顶头孢霉N2突变体的结构pcbC基因中的突变,从而导致头孢菌素的产生。功能性的α-氨基己二酰基-半胱氨酸-缬氨酸(ACV)合成酶由15.6 kb EcoRI-BamHI DNA片段编码,如互补于产黄青霉的ACV合成酶缺陷突变体所示。通过分别与pcbC和pcbAB基因内部探针进行Northern(RNA印迹)杂交,发现了1.15和11.4 kb的两个转录本。 11136 bp的开放阅读框位于pcbC基因的上游,该基因与11.4kb的转录起始和终止区域相匹配。它编码了3,712个氨基酸的蛋白质,推导的414,791先生。该基因的核苷酸序列与编码产黄青霉的ACV合成酶的pcbAB基因有62.9%的相似性。两种ACV合成酶中54.9%的氨基酸相同。在推定顶头孢霉ACV合成酶的氨基酸序列中出现三个高度重复的区域。每个与推导的产黄青霉ACV合成酶序列中的三个重复结构域相似,也与短芽孢杆菌的短杆菌肽合成酶I和酪氨酸合成酶I的氨基酸序列相似。这些区域可能对应于ACV合成酶蛋白中的氨基酸激活域。另外,两种真菌的ACV合成酶中都存在硫酯酶结构域。在多酶非核糖体肽合成酶与聚酮化合物和脂肪酸合成酶中存在的结构域之间发现了相似性。 pcbAB基因与pcbC基因相连,形成了早期的头孢菌素生物合成基因簇。

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