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144 1989 EMS Abstracts - • s --<br />

0http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />

416<br />

NOteS ^ ENVIRONMEN?AL MaU AGENESIS RESEARCH IN DEVELOPING COUNTRIES<br />

N .K . Notani, Biorcal Group, Bhabha Atanic Research Centre, Borbay 400085, India<br />

Indian reseaTcFfers-~trave wide interests <strong>and</strong> work on problens ranging from DNA repair,<br />

gene cloning, mutagens <strong>and</strong> entinutagens, test-syste•ns to nature of heritable variation in<br />

man, etc. Environ•nental Mutagen Society of India affiliated to IAEMS provides a major<br />

annual forun within the country <strong>and</strong> has also periodically organized courses, both international<br />

<strong>and</strong> national, for teaching of new techniques. Besides, it has cosponsored m eetings in related<br />

areas with other societies. In our Biorrsedical Group which m ay be considered as representative<br />

of research activities in the country has projects on mutagenicity testing, modification of<br />

mutagenicity by antrnutagens, mutation surveillance in control <strong>and</strong> high background radiation<br />

areas, cloning of DNA repair genes, Restriction Fragnent Length Pol)morphisn analysis<br />

<strong>and</strong> ostrn eiotic expogure leading to transn issible genetic dan age . Two of the researches<br />

are ~escribed below : i) DNA repair <strong>and</strong> gene cloning : We have self-cloned two genes, uvrl<br />

<strong>and</strong> mbo2, in Haenophi(us Tnt uenzae, u g e s carried on an 11 .3kb insert. This OIm1<br />

clone fully canple•nents UV-sensitive strain Uvr1- . A directedtnutagenesis system was<br />

developed which then induces mutations only in the 11 .3kb insert (Kanade <strong>and</strong> Notani,1987) .<br />

Another DNA repair gene mbo2 has also been cloned which fully canplenents UV-sensitive<br />

Mbo2- strain but not UvrT~strain . Subcloning of two EcoRl fraqnents yield clones; only<br />

the snaller of which partially canple•nents UV-sensitivity of Mbo2- strain (Mody, Joshi<br />

<strong>and</strong> Notani, 1989). ii) Newborn surve of o ulations residi in control <strong>and</strong> hi h bac round<br />

radiation areas: Georg e et ai have exa~n ne new orns for wn syn ro•ne <strong>and</strong><br />

'R>;L'h-06TSi1S88- date for Incidence related to m aternal age . Although, the data fror high<br />

background radiation areas are linited, these nevertheless see•n to be sinilar in incidence<br />

to the control area .<br />

CROSS ADAPTIVE RESPONSE BETVEEN HYDROGEN PEROXIDE AND ALDEHYDES IN E . croli. .<br />

T . NUNOSHIBA, M . HASHIMOTO, <strong>and</strong> H . NISHIOKA, Biochemistry . Doshisha University, Kyoto(Japan)<br />

417<br />

The phenomenon of the adaptive response that the bacterial cells acquire resistance to killing<br />

effect of a lethal dose of hydrogen peroxide(H202) . when they have been pretreated with<br />

its sublethal dose . has been noticed . Ve report here the existence of the adaptive response<br />

between H202 <strong>and</strong> aldehyde compounds . The phenomenon was na .ed by us as "Cross Adaptive<br />

Response" . The cells of E .2Qjj VP2 pretreated with a sublethal dose (30 or 80µM) of HzOz for<br />

30.in at 3TC acquired remarkable resistance to killing effect of for .aidehyde(FA) challenge<br />

at the concentration of B .M . The resistance acquirement due to pretreatment with a low concentration<br />

of H202 was similarly observed in the cases of challenge against the other aldehyde<br />

compounds such as chloroacetaldehyde . glutaraidehyde, glyoxal <strong>and</strong> methyl glyoxal . To elucidate<br />

the .echanism of the "Cross Adaptive Response", the effect of pretreatment with Hz02 on<br />

FA-sensitivity of ji . i strains with different DNA repair capacities was examined . The acquire.ent<br />

of the resistance was observed in VP7uvrA[V1f.l1] <strong>and</strong> ZA12[ug&] . but not in ZA80<br />

[recA] <strong>and</strong> CM561[IexA] . These results suggest that the "Cross Adaptive Response" Ray be attributed<br />

to induction of SOS genes coding some enzymes which are involved in reco .bination<br />

repair . the other unknown DNA repairs <strong>and</strong> aldehyde decomposition .<br />

418<br />

Cenotoxic effects of creosote oils : a relationship between ssutagenicity <strong>and</strong> the concentrations<br />

of A-S ring polycyclic aromatic hydrocarbons<br />

Yylund, L ., Heikkili, P ., Ji[rventaus, H ., Suhonen, S . . Hesso, A ., Himeill . !( . .<br />

Linnainsiaa, K . <strong>and</strong> Sorsa, tl .<br />

Institute of Occupational Health, Topeliuksenkatu •laA, Sy-00250 Helsinki, rinl<strong>and</strong><br />

Pour creosote oils iaported to Finl<strong>and</strong> from different countries were tested using<br />

the Ames test, the SCS-test with CHg-c .lis <strong>and</strong> an automated version of the SOS chrosotest<br />

. All creosote oils were positive using $ . tvohimurius TA98tS9aix . With strain<br />

TA100aS9aix only two of the creosote oils were positive . The SCS-test showed results<br />

similar to the Ames test results with strain TA98i89aix . The two oils that were positive<br />

both with TA98 <strong>and</strong> TAlOO were also positive in the 808 chromotest .The taped plate<br />

assay for compounds evaporating at 37•C gave negative results for all the four creosote<br />

oils . The creosote oils wre fractionated by distillation <strong>and</strong> the fractions were<br />

tested using the Ames test . Mostly, the wtagenic activities were observed in fractions<br />

with high-boiling compounds . The cheaical compositions of the creosote oils were<br />

determined using OC/!tS-techniques . It was found that the wtagenic activities with<br />

TA98a89mix correlated well (r .0 .96, p

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