McCormick S P, Hohn T M, Desjardins A E
Mycotoxin Research Unit, National Center for Agricultural Utilization Research, Peoria, Illinois 61604, USA.
Appl Environ Microbiol. 1996 Feb;62(2):353-9. doi: 10.1128/aem.62.2.353-359.1996.
An acetyltransferase gene (Tri3) was isolated from Fusarium sporotrichioides by complementation of a previously identified Tri3- mutant and shown to be closely linked to three other trichothecene biosynthetic pathway genes. Comparison of the Tri3 sequence with its cDNA revealed the presence of four introns. The Tri3 cDNA contains a 1,539-bp open reading frame that encodes a protein with a molecular mass of 57,418 Da. Regulation of Tri3 transcription in liquid cultures appeared identical to that of other trichothecene pathway genes. Disruption of the Tri3 gene resulted in the accumulation of deacetylated calonectrins rather than T-2 toxin. The results of whole-cell feeding experiments with Tri3- strains suggested that 15-O-acetylation is blocked. Cell-free feeding experiments confirmed that Tri3- strains are able to acetylate a trichothecene C-3 hydroxyl group but are unable to acetylate a trichothecene C-15 hydroxyl group. Our results show that Tri3 encodes an acetyltransferase that converts 15-decalonectrin to calonectrin.
通过对先前鉴定的Tri3突变体进行互补,从拟分枝孢镰刀菌中分离出一个乙酰转移酶基因(Tri3),并证明它与其他三个单端孢霉烯生物合成途径基因紧密相连。Tri3序列与其cDNA的比较显示存在四个内含子。Tri3 cDNA包含一个1539 bp的开放阅读框,编码一个分子量为57418 Da的蛋白质。液体培养中Tri3转录的调控似乎与其他单端孢霉烯途径基因相同。Tri3基因的破坏导致脱乙酰基卡洛内酯的积累,而不是T-2毒素。用Tri3菌株进行的全细胞喂养实验结果表明,15-O-乙酰化被阻断。无细胞喂养实验证实,Tri3菌株能够乙酰化单端孢霉烯的C-3羟基,但不能乙酰化单端孢霉烯的C-15羟基。我们的结果表明,Tri3编码一种将15-脱卡洛内酯转化为卡洛内酯的乙酰转移酶。