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用于控制基因工程微生物的模型自杀载体。

Model suicide vector for containment of genetically engineered microorganisms.

作者信息

Bej A K, Perlin M H, Atlas R M

机构信息

Department of Biology, University of Louisville, Kentucky 40292.

出版信息

Appl Environ Microbiol. 1988 Oct;54(10):2472-7. doi: 10.1128/aem.54.10.2472-2477.1988.

Abstract

A model suicide vector (pBAP19h), designed for the potential containment of genetically engineered microorganisms, was made by constructing a plasmid with the hok gene, which codes for a lethal polypeptide, under the control of the lac promoter. The vector plasmid also codes for carbenicillin resistance. In the absence of carbenicillin, induction of the hok gene in vitro caused elimination of all detectable cells containing the suicide vector; pBAP19h-free cells of the culture survived and grew exponentially. In the presence of carbenicillin, however, the number of cells containing pBAP19h initially declined after induction of hok but then multiplied exponentially. The surviving cells still had a fully functional hok gene and had apparently developed resistance to the action of the Hok polypeptide. Thus, high selective pressure against the loss of the suicide vector led to a failure of the system. Soil microcosm experiments confirmed the ability of a suicide vector to restrict the growth of a genetically engineered microorganism in the absence of selective pressure against the loss of the plasmid, with 90 to 99% elimination of hok-bearing cells within 24 h of hok induction. However, some pBAP19h-bearing cells survived in the soil microcosms after hok induction. The surviving cells contained an active hok gene but were not capable of normal growth even after elimination of the hok gene; it appears that a mutation that made them Hok resistant also reduced their capacity for membrane functions needed for energy generation and exponential cell growth. Thus, the model suicide vector was shown to be functional in soil as well as in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一种用于潜在控制基因工程微生物的模型自杀载体(pBAP19h),是通过构建一个质粒制成的,该质粒带有在乳糖启动子控制下编码致死多肽的hok基因。载体质粒还编码羧苄青霉素抗性。在没有羧苄青霉素的情况下,体外诱导hok基因会导致所有含有自杀载体的可检测细胞被清除;培养物中不含pBAP19h的细胞存活并呈指数生长。然而,在有羧苄青霉素的情况下,诱导hok后,含有pBAP19h的细胞数量最初下降,但随后呈指数增殖。存活的细胞仍然具有完全功能的hok基因,并且显然对Hok多肽的作用产生了抗性。因此,对自杀载体丢失的高选择压力导致该系统失效。土壤微宇宙实验证实了自杀载体在没有针对质粒丢失的选择压力时限制基因工程微生物生长的能力,在诱导hok后24小时内,90%至99%携带hok的细胞被清除。然而,诱导hok后,一些携带pBAP19h的细胞在土壤微宇宙中存活下来。存活的细胞含有活性hok基因,但即使在消除hok基因后也无法正常生长;似乎使它们对Hok产生抗性的突变也降低了它们产生能量和细胞指数生长所需的膜功能能力。因此,该模型自杀载体在土壤和体外均显示出功能。(摘要截短至250字)

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