Karelov D V, Kreneva R A, Érraĭs Lopes L, Perumov D A, Mironov A S
Genetika. 2011 Jun;47(6):856-61.
The nucleotide sequence of the ribC gene encoding the synthesis ofbifunctional flavokinase/flavine adenine nucleotide (FAD) synthetase in Bacillus subtilis have been determined in a family of riboflavin-constitutive mutants. Two mutations have been found in the proximal region of the gene, which controls the transferase (FAD synthase) activity. Three point mutations and one double mutation have been found (in addition to the two mutations that were detected earlier) in the distal region of the gene, which controls the flavokinase (flavin mononucleotide (FMN) synthase) activity. On the basis of all data known to date, it has been concluded that the identified mutations affect riboflavin and ATP binding sites. No mutations have been found in the PTAN conserved sequence, which forms the magnesium and ATP common binding site and is identical for organisms of all organizational levels, from bacteria too humans.
在一族核黄素组成型突变体中,已确定了枯草芽孢杆菌中编码双功能黄素激酶/黄素腺嘌呤二核苷酸(FAD)合成酶的ribC基因的核苷酸序列。在该基因的近端区域发现了两个突变,该区域控制转移酶(FAD合成酶)活性。在该基因的远端区域发现了三个点突变和一个双突变(除了先前检测到的两个突变),该区域控制黄素激酶(黄素单核苷酸(FMN)合成酶)活性。根据迄今已知的所有数据,得出的结论是,所鉴定的突变影响核黄素和ATP结合位点。在PTAN保守序列中未发现突变,该序列形成镁和ATP共同结合位点,并且对于从细菌到人类的所有组织水平的生物体都是相同的。