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Journal ArticleDOI

Acetone, methyl ethyl ketone, ethyl acetate, acetonitrile and other polar aprotic solvents are strong inducers of aneuploidy in Saccharomyces cerevisiae.

TLDR
It is proposed that the mutagenic agents act directly on tubulin during growth so that labile microtubules are formed which dissociate in the cold, and when cells are brought back to temperatures above the level critical for reassembly of tubulin and allowed to grow, faulty micro Tubulin cells are formed.
Abstract
A diploid yeast strain D61.M was used to study induction of mitotic chromosomal malsegregation, mitotic recombination and point mutation. Several ketones (including acetone and methyl ethyl ketone) and some organic acid esters (including the methyl, ethyl and 2-methoxyethyl esters of acetic acid) and acetonitrile strongly induced aneuploidy but not recombination or point mutation. Only diethyl ketone induced low levels of recombination and point mutation in addition to aneuploidy. Related compounds were weak inducers of aneuploidy: methyl n-propyl ketone, the methyl esters of propionic and butyric acid, acetic acid esters of n- and iso-propanol and ethyl propionate. No mutagenicity was found with n-butyl and isoamyl acetate, ethyl formate, acetyl acetone (2,5-dipentanone) and dioxane. Methyl isopropyl ketone induced only some recombination and point mutation but no aneuploidy. Efficient induction was only observed with a treatment protocol in which growing cells were exposed to the chemicals during a growth period of 4 h at 28 degrees C followed by incubation in ice for more than 90 min, usually overnight for 16-17 h. Aneuploid cells could be detected in such cultures during a subsequent incubation at growth temperature if the chemical was still present. Detailed analysis showed that there was a high incidence of multiple events of chromosomal malsegregation. It is proposed that the mutagenic agents act directly on tubulin during growth so that labile microtubules are formed which dissociate in the cold. When cells are brought back to temperatures above the level critical for reassembly of tubulin and allowed to grow, faulty microtubules are formed.

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Citations
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Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission, Flavouring Group Evaluation 22: Ring-substituted phenolic substances from chemical groups 21 and 25: Question No EFSA-Q-2003-165

TL;DR: The Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (the Panel) is asked to advise the Commission on the implications for human health of chemically defined flavouring substances used in or on foodstuffs in the Member States as mentioned in this paper.
Journal ArticleDOI

High levels of chromosome instability in polyploids of Saccharomyces cerevisiae.

TL;DR: The yeast Saccharomyces cerevisiae was used to study the genetic consequences of polyploidy and it was found that as ploidy increased, the frequency of loss of a single chromosome VII increased: loss of one copy of chromosome VII occurred at a rate nearly 30-fold higher in triploids and approximately 1000-foldHigher in tetraploids than in the diploid.
Journal ArticleDOI

Effect of Milk Allowance on Concentrate Intake, Ruminal Environment, and Ruminal Development in Milk-Fed Holstein Calves

TL;DR: The ruminal environment of young calves fed a barley-based starter concentrate was characterized by a low ruminal pH and high VFA concentration regardless of the milk allowance, concluding that the milk allowances changed the body composition of the calves.
References
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Journal ArticleDOI

Structural rearrangements of tubulin and actin during the cell cycle of the yeast Saccharomyces.

TL;DR: The distribution of actin and tubulin during the cell cycle of the budding yeast Saccharomyces was mapped by immunofluorescence using fixed cells from which the walls had been removed by digestion to suggest that it may have a role in the localized deposition of new cell wall material.
Book

Handbook of mutagenicity test procedures

B. J. Kilbey
TL;DR: This book consists of 39 chapters and some of the titles are: Bacillus subtilis repair test, Induced reversion using human adenovirus, The fluctuation test in bacteria, Chemical mutagenesis with diploid human fibroblasts, The specific locus test in the mouse, The bone marrow micronucleus test, and Sperm morphology in testing in mice.
Book ChapterDOI

[36] Preparation of tubulin from brain

TL;DR: Two methods for preparing tubulin are presented: purification by cycles of assembly and disassembly followed by chromatography on phospbocellulose and modified Weisenberg procedure, each of which yields several hundred milligrams of purified protein.
Journal ArticleDOI

Purification of yeast tubulin by self-assembly in vitro.

John V. Kilmartin
- 09 Jun 1981 - 
TL;DR: The in vitro yeast tubulin assembly is inhibited by the fungicide methyl N-(benzimidazol-2-yl)carbamate, the active component of benomyl, whereas in vitro brain 6S tubulinAssembly is resistant, which suggests that the inhibitory effect of Benomyl on yeast cell division is due to its antimicrotubule action.
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