Kim Jung-Mi, Song Ha-Yeon, Choi Hyo-Jin, So Kum-Kang, Kim Dae-Hyuk, Chae Keon-Sang, Han Dong-Min, Jahng Kwang-Yeop
Department of Bio-Environmental Chemistry, Wonkwang University, Iksan, 570-749, Republic of Korea.
J Microbiol. 2015 Jan;53(1):21-31. doi: 10.1007/s12275-015-4657-8. Epub 2015 Jan 4.
The null pigmentation mutant (npgA1) in Aspergillus nidulans results in a phenotype with colorless organs, decreased branching growth, delayed of asexual spore development, and aberrant cell wall structure. The npgA gene was isolated from A. nidulans to investigate these pleiomorphic phenomena of npgA1 mutant. Sequencing analysis of the complementing gene indicated that it contained a 4'-phosphopantetheinyl transferase (PPTase) superfamily domain. Enzymatic assay of the PPTase, encoded by the npgA gene, was implemented in vivo and in vitro. Loss-of-function of LYS5, which encoded a PPTase in Saccharomyces cerevisiae, was functionally complemented by NpgA, and Escherichia coli-derived NpgA revealed phosphopantetheinylation activity with the elaboration of 3'5'-ADP. Deletion of the npgA gene caused perfectly a lethal phenotype and the absence of asexual/sexual sporulation and secondary metabolites such as pigments in A. nidulans. However, a cross feeding effect with A. nidulans wild type allowed recovery from deletion defects, and phased-culture filtrate from the wild type were used to verify that the npgA gene was essential for formation of metabolites needed for development as well as growth. In addition, forced expression of npgA promoted the formation of conidia and cleistothecia as well as growth. These results indicate that the npgA gene is involved in the phosphopantetheinylation required for primary biological processes such as growth, asexual/sexual development, and the synthesis of secondary metabolites in A. nidulans.
构巢曲霉中的无色素突变体(npgA1)导致一种表型,其器官无色、分支生长减少、无性孢子发育延迟且细胞壁结构异常。从构巢曲霉中分离出npgA基因,以研究npgA1突变体的这些多形现象。互补基因的测序分析表明,它含有一个4'-磷酸泛酰巯基乙胺基转移酶(PPTase)超家族结构域。对由npgA基因编码的PPTase进行了体内和体外酶活性测定。酿酒酵母中编码PPTase的LYS5功能缺失由NpgA在功能上互补,并且大肠杆菌来源的NpgA显示出对3'5'-ADP的磷酸泛酰巯基乙胺化活性。npgA基因的缺失在构巢曲霉中完全导致致死表型以及无性/有性孢子形成和色素等次生代谢产物的缺失。然而,与构巢曲霉野生型的交叉饲养效应允许从缺失缺陷中恢复,并且来自野生型的分阶段培养滤液用于验证npgA基因对于发育以及生长所需的代谢产物的形成是必不可少的。此外,npgA的强制表达促进了分生孢子和闭囊壳的形成以及生长。这些结果表明,npgA基因参与了构巢曲霉生长、无性/有性发育以及次生代谢产物合成等主要生物学过程所需的磷酸泛酰巯基乙胺化。