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[季也蒙毕赤酵母中核黄素生物合成的遗传控制。新调控基因RIB81的检测]

[Genetic control of riboflavin biosynthesis in Pichia guilliermondii yeasts. The detection of a new regulator gene RIB81].

作者信息

Shavlovskiĭ G M, Babiak L Ia, Sibirnyĭ A A, Logvinenko E M

出版信息

Genetika. 1985 Mar;21(3):368-74.

PMID:3838729
Abstract

The properties of mutants resistant to 7-methyl-8-trifluoromethyl-10-(1'-D-ribityl)-isoalloxazine (MTRY) were studied. The mutants were isolated from a genetic line of Pichia guilliermondii. Several of them were riboflavin overproducers and had derepressed flavinogenesis enzymes (GTP cyclohydrolase, 6.7-dimethyl-8-ribityllumazine synthase) in iron-rich medium. An additional derepression of these enzymes as well as derepression of riboflavin synthase occurred in iron-deficient medium. The characters "riboflavin oversynthesis" and "derepression of enzymes" were recessive in mutants of the 1st class, or dominant in those of the 2nd class. The hybrids of analogue-resistant strains of the 1st class with previously isolated regulatory mutants ribR (novel designation rib80) possessed the wild-type phenotype and were only capable of riboflavin overproduction under iron deficiency. Complementation analysis of the MTRY-resistant mutants showed that vitamin B2 oversynthesis and enzymes' derepression in these mutants are caused by impairment of a novel regulatory gene, RIB81. Thus, riboflavin biosynthesis in P. guilliermondii yeast is regulated at least by two genes of the negative action: RIB80 and RIB81. The meiotic segregants which contained rib80 and rib81 mutations did not show additivity in the action of the above regulatory genes. The hybrids of rib81 mutants with natural nonflavinogenic strain P. guilliermondii NF1453-1 were not capable of riboflavin oversythesis in the iron-rich medium. Apparently, the strain NF1453-1 contains an unaltered gene RIB81.

摘要

对耐7-甲基-8-三氟甲基-10-(1'-D-核醇基)-异咯嗪(MTRY)的突变体特性进行了研究。这些突变体是从季也蒙毕赤酵母的一个遗传品系中分离得到的。其中一些是核黄素过量生产者,并且在富铁培养基中具有去阻遏的黄素生成酶(GTP环化水解酶、6,7-二甲基-8-核醇基芦竹碱合酶)。在缺铁培养基中,这些酶以及核黄素合酶会进一步去阻遏。“核黄素过度合成”和“酶的去阻遏”性状在第一类突变体中是隐性的,而在第二类突变体中是显性的。第一类抗类似物菌株与先前分离的调节突变体ribR(新命名为rib80)的杂交体具有野生型表型,并且仅在缺铁条件下能够过量生产核黄素。对耐MTRY突变体的互补分析表明,这些突变体中维生素B2的过度合成和酶的去阻遏是由一个新的调节基因RIB81的损伤引起的。因此,季也蒙毕赤酵母中的核黄素生物合成至少受两个负作用基因调控:RIB80和RIB81。含有rib80和rib81突变的减数分裂分离子在上述调节基因的作用中未表现出加性效应。rib81突变体与天然非黄素生成菌株季也蒙毕赤酵母NF145–1的杂交体在富铁培养基中不能过量合成核黄素。显然,菌株NF145–1含有未改变的基因RIB81。

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