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利用噬菌体λ cIts857诱导试验进行致癌物筛查。

Screening of carcinogens with the prophage lambda cIts857 induction test.

作者信息

Ho Y L, Ho S K

出版信息

Cancer Res. 1981 Feb;41(2):532-6.

PMID:6449995
Abstract

The prophage lambda cIts857 induction test with Escherichia coli K12 envA uvrB as the lysogen has been successfully applied to the screening of sparingly water-soluble carcinogens that have been dissolved in dimethyl sulfoxide and metabolically activated with liver enzymes induced either with Aroclor 1254 or phenobarbital. Growth of noninduced lysogenic cells during the test was suppressed with ampicillin, with resultant increase of sensitivity of the test. The maximum inducing activity observed was about 50% of the complete induction level attained with water-soluble carcinogens that did not require metabolic activation. High sensitivity was achieved with the use of the lambda cIts857 prophage strain. In several instances where the Ames Salmonella-microsome test has failed to confirm the carcinogenicity of the respective carcinogens, this induction test has provided a better correlation. Of the carcinogens tested, only one false negative, namely, cyclophosphamide, was encountered. In contrast, the use of the wild-type prophage lambda strain resulted in low sensitivity. The adoption of the endolysin assay technique for the assessment of induction has greatly simplified the procedures and has permitted the screening test to be performed quickly and economically.

摘要

以大肠杆菌K12 envA uvrB作为溶原菌的λ噬菌体cIts857诱导试验已成功应用于筛选溶解于二甲基亚砜并经用Aroclor 1254或苯巴比妥诱导的肝酶进行代谢活化的微溶于水的致癌物。试验期间,用氨苄青霉素抑制未诱导的溶原细胞生长,从而提高了试验的灵敏度。观察到的最大诱导活性约为不需要代谢活化的水溶性致癌物所达到的完全诱导水平的50%。使用λcIts857噬菌体菌株实现了高灵敏度。在几例艾姆斯沙门氏菌-微粒体试验未能证实相应致癌物致癌性的情况下,这种诱导试验显示出更好的相关性。在所测试的致癌物中,仅遇到一例假阴性,即环磷酰胺。相比之下,使用野生型λ噬菌体菌株灵敏度较低。采用内溶素测定技术评估诱导作用极大地简化了程序,并使筛选试验能够快速且经济地进行。

相似文献

1
Screening of carcinogens with the prophage lambda cIts857 induction test.利用噬菌体λ cIts857诱导试验进行致癌物筛查。
Cancer Res. 1981 Feb;41(2):532-6.
2
Prophage lambda induction of Escherichia coli K12 envA uvrB: a highly sensitive test for potential carcinogens.大肠杆菌K12 envA uvrB的噬菌体λ诱导:一种对潜在致癌物的高灵敏度检测方法。
Proc Natl Acad Sci U S A. 1976 Oct;73(10):3700-4. doi: 10.1073/pnas.73.10.3700.
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Evaluation of the Escherichia coli K12 inductest for detection of potential chemical carcinogens.用于检测潜在化学致癌物的大肠杆菌K12诱导试验的评估
Mutat Res. 1984 Jun;130(3):141-51. doi: 10.1016/0165-1161(84)90116-x.
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[Mutagenic effect of o-methylhydroxylamine on the prophage and extracellular phage lambda].邻甲基羟胺对原噬菌体和细胞外λ噬菌体的诱变作用
Mol Gen Mikrobiol Virusol. 1985 May(5):23-8.
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Effect of glutathione on UV induction of prophage lambda.谷胱甘肽对λ原噬菌体紫外线诱导的影响。
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Induction of a stable, heritable epigenetic change by mutagenic carcinogens: a new test system.诱变致癌物诱导稳定、可遗传的表观遗传变化:一种新的测试系统。
IARC Sci Publ. 1980(27):243-55.
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[Mutagenic action of nitrous acid on prophage lambda].[亚硝酸对λ原噬菌体的诱变作用]
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Induction of prophage lambda by chlorinated organics: detection of some single-species/single-site carcinogens.氯化有机物诱导原噬菌体λ:一些单物种/单位点致癌物的检测
Environ Mol Mutagen. 1992;19(2):98-111. doi: 10.1002/em.2850190204.
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[Mechanism of non-tandem integration of prophage phi 80 into the chromosome of the wild-type Escherichia coli].[噬菌体φ80非串联整合到野生型大肠杆菌染色体中的机制]
Genetika. 1985 May;21(5):707-15.
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Mutagenesis assays with bacteria.细菌诱变试验
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引用本文的文献

1
Phage Therapy: Beyond Antibacterial Action.噬菌体疗法:超越抗菌作用
Front Med (Lausanne). 2018 May 23;5:146. doi: 10.3389/fmed.2018.00146. eCollection 2018.
2
SOS chromotest, a direct assay of induction of an SOS function in Escherichia coli K-12 to measure genotoxicity.SOS 显色试验,一种直接检测大肠杆菌 K-12 中 SOS 功能诱导以测量遗传毒性的方法。
Proc Natl Acad Sci U S A. 1982 Oct;79(19):5971-5. doi: 10.1073/pnas.79.19.5971.
3
Antitumor activity of platinum complexes.铂配合物的抗肿瘤活性。
Cancer Chemother Pharmacol. 1983;10(3):145-9. doi: 10.1007/BF00255749.
4
Action of citrinin on bacterial chromosomal and plasmid DNA in vivo and in vitro.桔霉素在体内和体外对细菌染色体及质粒DNA的作用。
Appl Environ Microbiol. 1986 Dec;52(6):1273-9. doi: 10.1128/aem.52.6.1273-1279.1986.
5
DNA-damaging activity of patulin in Escherichia coli.展青霉素在大肠杆菌中的DNA损伤活性。
Appl Environ Microbiol. 1986 Nov;52(5):1046-54. doi: 10.1128/aem.52.5.1046-1054.1986.