SCIENTIFIC ABSTRACT MARDER, B.B. - MARDASHEV, S.R.

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• Collection: Scientific Abstracts
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• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

~- MAWER B
Antibody formation in employees of roentgenological departments
vaccinated -Ath live tularemia vaccine. Med. rad. 6 no.1:13-15
161. (KIRA 14:3)
(TULAREMIA) (RADIATION-PHMIOLOGICAL EFFECT)

MRDBRI B.Bi, po4ol-kovnik meditsinskoy sluzhby
Second interinstitute conference on problems of radiation microbiology
and imm-mology. Voen.-med. zhur. no.5:92-93 MY 161. (1-URA- 1/,: 8)
(PJ.DIOBIOLOGY)

LENTSNER. A.A.; Tu.P.
Problem of the possibility of transformation of para-agglutinating
strains from river water into typical intestinal pathogens. Zhur.
mikrobiol.epid.1 immun. 30 no.7:68-71 JI 159. (MIRA 12:11)
(BAr.TXRIA)
(WATXR - microbiology)

HARM D-2.-V-podpolkovnik med. sluzhby; LEBTSUM, A.A.. k-aDitAn med. sluzhby,
~knnd. mod. nauk; TITOVA-MARDYM, V.L., kpnd.med.nsuk
Bnaterioscopy as a method for determining bneteria in the air Rnd water.
Voon.med.zhur. no.9:51-54 S 157. (MEU. 11:3)
(WAM, microbiology,
bacterioscopy (Rus)
(MR. microbiology,
same)

"At the same time, intracutaneous tularin was rather highly reacto-
..genic as compared with cutaneous tularin. This was demonstrated by the
large percentage of acutely positive reactions.,
"Thus., the allergic properties of cutaneous tularin prepared from
a vaccine strain of tularemia bacteria were somewhat exceeded by the al-
lergenic properties of intracutaneous tularin. However, experience
showed that with the use of the cutaneous tularin allergenic test, more
than 75% of persons inoculated were found to be immune. This led to the
conclusion that-cutaneous tularin can be used for determining the immme
condition of inoculated groups and that the method of its application is
simpler by far than the~method of applying intracutaneous tularin."

A q,6 G- /~
Tht, Intrucutandous tularin test vau performed- according to the usual
method, and the cutaneous tularin test on the under surface of the forearm
according to the Popov method used at the Saratov institute., 'Mikrob-I The
procedure for the cutaneous tularin test was as follows: after treatment
~of the skin with alcohol, two drops of tularin were applied to the skin 2-3
em apart by shaking from an open ampule; shallow scratches were inflicted
.through the drops with a vaccine stylus, and the tularin was rubbed into
the scratches with the ribbed surface of the utylus.
"The reaction was evaluated by a five-point system: acutely positive,
.positive, weakly positive, doubtful, and negative.
"On comparison of the aforementioned tularins., the predominance of
,doubtful and particularly of negative reactions to cutaneous tularin at-
tracted attention; 370 reactions in all were carried out with cutaneous
tularin, out of which 45.1% were positive, 101% were acutely positive,
14.9% were negative, and 9.7% were doubtful. Of 168 intracutaneous tula-
rin testsl 63.1% were positive, 14-0were-Acutely positive, 2.7% were
negative., aIA were d6ubtftl

A iq ig, 6
~1;om - ~~tiye Testin Properties-of Cutaneous
,-p
and Intracutaneous T~arih When Used for the Purpose of Detect-
ing Immune Strata Among Persons Inoculated," by E. H. Belostot-
skayn,,D_.B. Na-,rdar, Ye. B. Maksimova and Ya. L. Gendellman,
Kaliningrad Antitularemia Station and Military Laboratory of the
Baltic Coast Military District, Zhurnal Mikrobiologii, Epidemio-
logii i Immunobiologii Supplement, 1957, PP 33-34
"Mass testin.t, of cutaneous tularin series No 10, prepared from a vac-
cine strain of tularemia bacteria according to A. N. Popovals method in
the Tularemia Laboratory of the Institute imeni Gamaleya, was carried out
in 1955 to study the allergenic properties of this series of tularin and
to detect i-miine strata among inoculated persons. Tests with the usual
intracutaneous tularin series No 31 were simultaneously set up for com-
parizon.
"Some 523 persons between the ages of 18 and 23 were observed. In-
oculations were performed on 21 and 22 March 1955 with dry antitularemia
vaccine series No 481, 484, and 474, and tests were carried out 2 montha
after vaccination.
"Results of the cutaneous tularin test were checked after 24, 48
hours,-andafter-72 hoursin persons who exhibited doubtful results. Re-
sultm (.a+ the_~ .14tftcutaneous tularin test weritchecked:vithln 48 hours.

BUBLIK, P.Te.; 'KARDER, A.TS.; VASIKO, T.P.; BAMMINSKAYA, O.A., spetared.;
VASIL I CHRBYSHEVA, Ye.A., tekhn.red.
(Purifying feed molasses using clarifiers; practices of yeast
enterprises of the Ukraiae] Osvetlenie ko=ovoi patoki a pri-
meaeniom klarifikatorov; opyt drozhzhavykh predpriiatii Ukrainy.
Moskva, Pishchapromizdat. 1957. 15 p. (MIRA 12:5)
(Ukraine--Kolasses) (Toast) (Separators (Machines))

K4F,n-TNSFIY Ir. kandl, teekhr_ naul<
-1 - - ~ -- - , Y.. .-j- 1.
IJIVerall ra-,ee',igr - ZL" C,,l ~,-' f 1 or eratjlcns in st.4 ~ -T I ~ :,,
I - - i I I
Reah. transp. 24 nn.3~ '6.) a " 1! 18, 5 .

MRNVWIS~Wimi~rPrOk~O' ~vich; SHELUCHENKO, V.M.., red.; VOLCHOK,
K.M., tekhn. red.
(Manufacture and repair of the fuel systam equipment for marine
diesel engines)Izgotovlenia i remont toplivnoi apparatury sudo-
vykh dizelei. Leningrad, Izd-vo "Rechnoi transport," 1962. 173 P.
(MIRA 16:1)
(Marine diesel engines--Fuel system)

GUSEV, Mikhail Hikolayevich. prepodavatell; ZILIST, Petr Sigizmundovich,
prepodavatell; LEV. Tevgeniy Semenovich. prepodavatell; LOPYREV,
Hikolay Kirillovich, prepodavatell. XARMSUT...VladimIrPro-,
.kqh. prepodavatell; NMOV. 74tr Petrovich, prepodavatel';
HINITIN, Gennadly Hikhaylovich, prepodavatell; CHMO, V.H.,
dotsent, kand.takhn.nauk, retaenzent; BELOV. Ii.M.. inzh., retsen-
zent; GOWVAHOV, II.T.. red.; VOLCHOK, K.M., takhn.red,
[Technology of marine engineering and ship repairs] Takhriologiia
sudovogo, mashinostroanila i sudoremonta. Pod obahchei red. M.N.
Guseva. Leningrad. Izd-vo 'Rechnoi transport,* Laningr.otd-nia.
Pt.2. [Technology of ship repairs] Tekhnologiia sudoremonta.
ig6o. 47o p. NM 13:4)
1. Kafedra tekhnologli sudostroyeniya i sudoremonta Leningradskogo,
instituta vodnogo, transports (for %sev, Zilist, Lev, Lopyrev,
Rardenskiy, Remkov, Nikitin).
('Ships--Haintenance and repair)

KARMSKITj-UadiMir-Pr.Okop~78vi0h; GOLOVAHOV, N.V., red.; VOLCHOK. K.K.,
- takhn.red.
[Repair of the fuel equipment of marina diesel engines] Remont
toplivnoi apparatury sudovykh dizelei. Leningrad. Izd-vo 'KRachnoi
transport.0 Leningr.otd-nia. 1960. 117 P. (KIRA 13:10)
(Karin@ diesel engines-Maintanaace and repair)

MMENSKIY, V.P., kand.tekhn.nauk, dotsent
Applying G-.F. Proskura's method to the desiFn of axial exhaust farS
Trudy L11VT no.26:lq2_zoo 159. 0AIRA lip.. gr
(Ships--Heating and ventilation) (Exhaust systems)

,,~HMMISKIY, V.P., kand.takhn.rkauk
Technolog7 of building up worn precision pair elements for fuel
system equipment. Pi-oizv.-te" ~sbor. no-3:77-82 159.
(HM& 13: 10)
1. YAningradskiy institut; vodnogo transporta.
(Ships-Equipment and ouppUes)
(Instruments -*Kaintenance and repair)

I-MRVENSKIY9 V'y kand. tekhn. nauk, dotsent; BRYAKALOV, A., kand. tokhn. nauk
M. use-ful book. Mor. flot. 24 no.ll146 11 064, (MIPA 18:8)
1. Leningradskiy inatitut vodnogo transporta (for Bryakal.cv).

MARDASHKO., A.
flew method to determine -=,ussic acid in plants. Naulm i
zhyttia 11 no.22;37 D 16.1. - (MIRA 15-.2)
1. Uchenyy sekrotarg Vveqoyu-&uogo sele~Wqonno-genetiobeskogo
instituta imani T*.D.Ii-qenko.
~Hydroc-yanic aoid)
(Plants-Chemical analysis)

DEBOV, S.S.; HARDASHVE, S.R-; VORONOVS, A.Ya.
Effect of polyadenylic acid on the incorporation of lysine
into proteins by liver ribosomes in rats. Vop. med. khim.
10 no.6:635-637 N-D 164. (NaRA 19:1)
1. Kafedra biologicheskoy khimii I Moskovskogo ordena Lenina
meditsinskogo institute imeni Sechenova.

MARDASHEV, YU.S.
Quantum aspects of catalysis. Zhur. fiz. khIm. 39 na.8,-1817-
1822 Ag 165. (KRA 18,,9)
1. Moaknvskiy institut tonkoy khimlchef-koy tekhnnlogil.

MARDASFIEV, Yu.S.; AGRONOMOV, A.Ye.
Evaluation of the surface area of nickel in Hi/AI2()3 catalysts-
Zhur.fiz.khim. 36 no.8:1785-1787 Ag 162. (MIRA 15:8)
1. Moskovskiy gosudarstvannyy universitet imeni, Lomonosova.,
(Nickel catalysts)

S/18 621000100210011004
Selective assessment of the surface ... D22SYD302
Eimett et al, J. Amer. Chem. Soc. 59# 31O# 1937; P.N. Hill et al,
Ibid. 71, 2522, 1949; L. D'Or et alf J. Chem. Phys.9 51t 467t 19541
P.C. Tompkins, Disc. Paraday Soc, 541 548P 1958-
ASSOCIATION: Kafedra organicheskogo kataliza (Department of Organic
Catalysis)
SUBMITTED: May 8# 1961

3
~~9/62/000/002/001/004
D228/D302
5.1110
AUTHORS: Agronomov, A.Ye., and Mardashev, Yu.S,
TITLE: Selective assessment of the surface areas of metallic
catalysts on carriers
PERIODICAL: Moscow. Universitet,, VeEktnik. Seriya II, khimiya,
no. 2, 1962, 21 - 22
TEXT: The authors give more precise informatio, about their previ-
ous study of the chemisorption of phenol. This chows that the diffe-
rence in the size of the Ni part of the surface of the Ni/Al 203 ca-
talyst, calcd. by the method of direct detne and by the method of
comparing the chemisorption capacity of thiophenol on Ni-blackv
Ai2039 and Ni/Al 2031 amounts to only 15 %. Thus, it is concluded
that the method of comparison can be used to estimate selectively
the size of the Ni surface in N'IA203 catalysts. There are 1 table
and 8 references: 4 Soviet-bloc and 4 non-Boviet-bloce The referen-
ces to the English-language publications read as follows: P*H,
Card 112

AGRONOMOV, A.Ye.; WMASHEV, Yu.S.
dz__~
Structure and activity of supported nickel catalysts. Zhur.
fiz.khim. 35 no.9:2047-2051 161. (MIFLA. 14:10)
1. Moskovskiy gosudarstvennyy universitet imeni M.V. Lomonosova
i Institut organichtskoy khimii AN SSSR imeni N.D. Zalinskogo.
(Nickel' (Catalysis)

AGRO.ROMOV, A.Ye.; MARDASHEV, Yu.S.
Structure qnd activity of supported nickel catalysts. Part 1:
Structural changes of the catalyst support during the deposition
of nickel. Zhur.fiz.khim. 35 no.8:1666-1671 A 161.
&ia 3-4:8)
1. Moskovskiy gosudarstvennyy universitet imeni M.V. Lomonosova
i Institut or icheakoy khimi AN SSSR imeni N,D. Zelinskogo,
Mickel) (Catalysts)

PATRIUM. V.V.; BALAITDIN. A.A., akademik; KLABUliOVSKIT, Te.I.; MAPMSHEV, -
Yu.S.; MMIMVA. G.I.
Selectivit7 towards optical isomers of adsorbents fromed in the
presence of bacteria. DDkl.AII SSSR '132 no.4:850-852 Je '60.
(MIRA 13:5)
1. Institut organicheakoy khimii im. IT.D.Zelinakogo Akademii nauk
SSSR.
(Adsorbents) (Isomers)

1 8000?
The Dependence of Activation Energy on the Relative S/020~60/131/05/038/069
Adsorption Coefficient B004/ ~014
the benzene content of the starting mixture Of C6H6 + C6H12 (Table 2, Fig 2).
Proceeding from results obtained by other research workers, the authors discuss
this dependence and arrive at the following conclusion: As long as the dehydro-
genation of C6012 by maans of a nickel catalyst takes place at active points of
mean activation energy, which are moderately covered with C696, z2 does not
depend an the yield, no Howeverg as soon as these points are covered with a
larger amount Of COO the benzene has an inhibitory effect, and the relation
z2 - f(m) occurs, as may be seen when using catalysts with great values of z2.
Taking this into account, ane obtains a value of E for the second sampla, which
is in close agreement with the E-values of the other catalysts. Graphical
solving of the relation 0. - E - klOgz2 is recommended as another varianto The
authors refer to a publication by A. A. Balandin and Yu. K. Yurlyev (Ref 10).
There are 2 figures, 2 tables, and 12 references, 10 of which are Soviet.
ASSOCIATION: 9-oskovskiy gosudarstvennyy universitet im. X. V. Lomonosova
(Moscow State University imeni Me V. Lomonosov) Institut organi-
cheskoy khimii im. He D. Zelinskogo, Akademii nauk SSSR (Institute
of Organic Chemistry imeni N. D. Zelinskiy of the Academy of
Solenoes of the USSR)
SUBMITTED: December 28, 1959
Card 2/2

AUTHORS- Agronomov, A. Ye., Balandin, A. 1., 3)1020/60/131/05/038/069
Academician, iard~sh~_v, Yu. S. B004/BO14
TITLE: The Dependence Of Activation Energy on the Relative Adsorption
Coefficient
PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol 131, Hr 5, pp 1120-1122 (USSR)
TEXT: The authors of the article under review studied several nickel catalylts
within a wide temperature range, using dehydragenation of oyclohexane. The same
amount of nickel was applied to different oarrier substances (A120 9 silioa gel,
kieselguhr) in equal proportions by weight. The data listed in tMe i indicato
that the apparent activation energy, Q. calculated from the Arrhenius equation,
and the relative adsorption coefficient, z2, of the benzene being formed are
greatly dependent on the nature of the carrier substance. These two quantities
are interrelated by Q = E - klogZ2 (E and k are constants). This relationghip is
graphically represented in figure 1. For all catalysts under consideration it
was found that E.was constant and 14 kcal/mole approximately. This value cor-
responds to the initial coordinate of the straight line depicted in figure 1,
and thus represents the true activation energy. For nickel applied to silica
gel (second sample) it was found that the value Of z2 increased in dependence of
Card 1/2

AGRONOMOV, A.Te.; IURDASHEV, Tu.S.
Selective determination of Vie nickel onrface in nickel-alaminum
oxide catalysts, and their specific catalytic activity. Test.Mosk.
un.ser. 2: Khim. 15 no.1:25-34 160. (MIRA 13:7)
1. Kafedra organicheskogo kataliza Moskovskogo universiteta.
(Catalysts, Ifickel)

M. 9. ('r.rid c3ler.-., Scl - - "Irl- F-11-lcrt Of --r- carr',--r o,-. "?,.-
ilAFDASI-171) I., I
struteture and activity of nickel oatalysts". llloscow, 19(0. 11 iDp (Aced 3ci
,). 7elinskly
USSR, Tnst of Or,,anic Chem im N. I - ), 150 coplos (4, !qo 14, ln!'o,
1127)

Comparison of the Kinetic Relative Adsorption SOV/20-127-2-25/70
Coefficients With Those Determined According to the BE.? Equatton
zBET are equal is assumed tc
statement (Ref 12) that the
intensity are catalyti-cally
2 tables, and 12 referencea,
confirm the second author's
places with a mean adsorption
active. There are 1 figurep
11 of which are Soviet.
ASSOCIATION: Moskovskiy gosudarstvenn;yy aniversitet im. M. V. Lomonosova
Noscow State University imeni, 9. V. Lomonosov)
Institut organicheskoy khimii im. H. D. Zel.inskogo Akademii
nauk SSSR
(Institute of Organic Chemistry imeni N. D. Zelinskiy of the
Academy of Sciences, USSR)
SUBMITTED: April 29, 1959
Card 4/4

Comparison of the Kinetic Relative Adsorption SOV/20-127-2-25/70
Coefficients Vith Those Determined According to the BET Equation
temperaturep then again with pure cyclohexane, This experiment
confirmed the observation of reference 11 that the aotivation
energy is not chan&red up to a mixture containing 101% berizene
for the catalyst Ur 3). The two series of the values
~AC according to adsorption-, kinetic data respectively) are
very adjacent in the columns 3 and 4 of table 1. Thus, the
BET equation may be used in the case of the cyclohexane
' (Fig 1). The general equation of the kinetics
dehydrogenation'
of the monomolecular roactions (Ref 4) holds as well in the
investigated region of the mixture composition, as it follows
from the constancy of z (Table 2). The relative AC of the
catalytic active centers ti= out to be practically equal to
the relative AC of the entire surface. The fact that zk and
Card 3/4

Comparison of the Kinetic Relative Adsorption SOV/20-127-2-25/70
Coefficients With Those Determined According to the BET Equation
interesting to carry out the comparison given in the title.
The absolute AC differ according to reference 7 by two orders
of magnitude. The authors used the dehydrogenation reaction
of oyolohexane on Ni-catalysts (the latter on carriers). The
BUT-AC were graphically determined from the equation (1).
The straight lines for the catalysts Nr 1 and 2 (Table 1) are
given in figure 1 as an example (5 catalysts were used and
their method of production is described here). AC according to
BET (a BET) for benzene and cyclohexane were computed from the
tangent of the angle of gradient of this straight line; their
relation could be called the relative AC-BET (z (Table 1
BET)
columns 1-3)o The kinetic relati-!jre AC were determined from the
equation (2). The reaction mentioned was carried out according
to the method of reference 10. The catalyst was used in a certain
quantity (volume V) so that the transformation did not exceed
30%. The equation (2) was transformed into (3) in the
experiments with pare cyclohexane. Furthermore, the experiment
Card 2/4 ras carried out with a mixture (with benzene) at the same

50) SOVI/20-127-2-25/70
AUTHORS: Agronomov, A. Ye., Balandin, A. A., Academician,
TITLE: Comparison of the Kinetic Relative Adsorption Coefficients
With Those Determined According to tho BET Equation
PERIODICAL: Doklady Akademii nauk SSSR, 1959, Vol 127, Nr 2, pp 325-328
(USSR)
ABSTRAM The BET equation of the polymolecular adsorption which takes
into account the interactions between adsorbent and adsorbed
substance in the first layer and is related to the entire
surface was derived in reference 1 (1938) (1), Its graphic
solution makes the determination of the adsorption coefficient
(AC) o possible. The second author in 1942 (Ref 2) derived an
equation of the kinetics of the monomolecular reaction in a
discharge system. A calculation method of the relative
adsorption coefficient from kinetic data is given as well.
This method made the determination of the value of these
coefficients on the catalytically active centres of the
surface possible. The equation (2) (identical with the equation
(52) in reference 5) may be used for the determination of the
Card 1/4 relative adsorption coefficients from kinetic data.It was

fV)hRDqS14Ev, Yo.s ,
USSR/Chemistry - Catalysts FD-2171
Card 1/1 Pub 129-11/20
Author Agronomov, A. Ye. and Mardashev, Yu. S.
Title Investigating the rela ship between catalytic activity of Ni-A1203
and its structure and quantity of nickel in the catalyst
Periodical Vest. blos. un., Ser. f izikomat. i yest. nauk, 10, No 2,83-91, Mar 1955
Abstract Studied the cyclohexane dehydrogenation reaction over a nickel on
A1203 catalyst with varying amounts of nickel. Established that
the most active catalyst was one having 36.5% nickel by weight.
The'apparent activation energy decreases with increasing amounts
of nickel. Using the adsorption method of investigation, established
that the specific surface of the catalyst remains equal up to 36.5%'
nickel and then decreases with further additions of nickel. The
porosity of the catalyst depends on-the amount of nickel present.
Graphs; tables. Twenty-one references (eighteen USSR).
Institution Chair of Organic Catalysis
Submitted June 24, 1954

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MuliDASHEV, .3,R.; SEMIN.L~,
(,rystahine histinine fie-2arboxylase oLtralned fr= !~icr-,C.-cclis
L I
Sp. n. Dakl. AN SSSR 1~b no, 2si,65-466 lt( '64. (11'11~lk 11-1:771
1. Institu. i me,iitsinskoy khl-rr-*i AU,21
2. Pjey.%tvitF-,I'ryy chlt~n AN'.1 S';~'..R (for Mardashev,'.

MARDASHEV%, S.R-.; BUROBIN, V.A.
- . - - c, -1 - - -.-, - -
Determination of urocanase in the blood in carbon tetrachloride
poisoning. Vop. med. khim. 9 no.1:93-94 Ja-F 163.
(MIRA 17:6)
1. Kafedra biokhimii I Moskovskogo ordena Lenina meditsinskogo
instituta imeni I.M. Sechenova, Moskva.

KARDASHKV, S.R.; LEaWl, M.I.; BENMOVICH, M.S.
Glut-amine transaminase in brain preparations and in cells of
a strain of a differentiated human astrocytoma. Vop. med. khim.
8 no.5-.547 --549 S-0162 (MM 17:4)
1. Kafedra biakhimii Moskovskogo ordene, Lenins. meditsinskogo
instituta, immi I.M.Sechenova i laboratoriya kulltivirovaniya
tkaney Instituta eksperimentaltnay i klinicheskoy onkologii
AM SSSRY HbWm.

MARDASHEV, S.R.j YAROVAYA, L.M,
Guanosine monophospha te-syn the tase reaction of Z.~.-oli. LTkr.biokhim.
zhur. 37 no.5a751-760 165- (MIRA 18:10)
1. Institut biologicheakoy i meditsinskoy khimil All-111 SSSR, Moskva.

MARDASHEV, S.R.; SOAOVNINA, Ya.M.
,Wynthesis of hydroxamie acla'S rrom dl~~rrbcyyliu amino acidp
and their am'-des in Saccharomyces cer~-Vistae. .1-filt-roblol-Og-lia
34 no.1:47-52 Ja-F 165. 'kl4TFU-- 18:7)
1. Institut blologichaskoy i neditzainskoy knimil ALDI SSSR.

MARDASHEV, S.R.t SEMINA, L.A.,, SOUINAS A.M~
Amino acid nomposition of histidine decarboxy lase. Blokhlmila
30 no.6s1179-1181 N--D 165. (MIRA jq~~-J)
1. Laboratoriya enzimologii Instituta b1olog-Icheskoy i medltslniskoy
khimii OV SSSR 1 kafedra biokhimli Pervogo Moskovskogo meditsinskogo
instituta, Moskva, Submitted January 21, 1965.

5SEMINAY L.A.; WMASEEV, 55.R.
Purlftca~-ior, and cr;-t,'~.aI24sation of minrcb�al ti!-stlidire
decarboxylpas,,~. Bielchiraiia 30 no.1-100-106 je-Y t65.
MIRA 18- 6)
. Laboratoriya enzimolag-li-i -tnstituta hlologicheakoy i meditsinsko-,
L
khllml:~ AM SSSR~ Moakva.

ZBARSKIY, Boris Illich (deceased]; IVANOV9 Illya Il'ich3
MARDASHEV, Sergey Rufovich; ILIIN, V.S.. red.
(Biological chemistry] Biologicheakaia khimiia. 4. izd.,
ispr. i dop. Leningrad, Meditsina, 1965 519 P.
iMIRA 18.6)

MARDASH-
EV DEBOV, S.S., red.
~-I
[Some problerx- in the regu2ation of metaboliev-, and natural
polymers] Nekotorye problemy regu-liatsii obmena veshchastv
i prirodnye polimery. Mosk-va, Meditsina, 1965. 82 p.
(MIRA 18:9)

MARDkSI9,T, S.R.
Natural polymer5. Priroda 53 no.9z35-45 164. 047!.A
1. Deystvitellnyy chlen AM SSSR.

GARAN, S.I.; MAYMIND, V.I.; MALRDASHEV, S.R.
.1
Synthesis of the sodium salt of,rarbamylhomoderine and its amide. Dcki.
AN SSSR 154 no.6:1374-1375 F 164. (MIRA 17:2)
1. Institut, btologichaskoy i 'meditsinslcoy khimii AMN SSSR. 2. Daystvi-
tellnyy chlen AMN SSSR (for Mardashev).

GALEGOV, G.A.; SERGFYFVA, M.A.; MARDASIIEV S.R
I
Synthesis of DIN!5--beta-mthy-laspartic acid. Bickhimi-ia 29 no.3:
497-501 MY-Je 164. (MIRA 18:4)
1. Institut biologicheskoy i meditsinskoy khimii AMN SSSR, Moskva.

MARDASHEV, S.R.
"a t ;. 1 .1
I, =al polymc-s. their b-'ological and med4-al `,apo"~ance. Voo.med.
khim. 10 no.3-227-238 '-~y-Je 164. (MIIR~ 18,,2)1

GALEGOV, G.A.; MAO-O)ASHEV, S.R.
L ~ 1, , 11 A I L.
Effect of D I homfluorrivallne jjri~w'h Cf
Vop.ined.lchim. 10 no.2:216-217 Mir-Ap '64. (MIRA .18:1)
1. lAboratoriya enzin,ololgii Tnstituta biologicheskoy i mpdliusirlskoy
Idi-bid! AMN SSSR, Moskva.

DEBOV, S.S.; NIAIEDA001011, S.R.; Ye.V.
R-41bonueleic ac-!d Toly- rizatIon ar-*,,4.v-"ty of
from the rat liver and from Ehrlich ascites cancer in mice.
Vop. med. khim. 10 no.1,92-94 Ta-F 161,.
(NIRA 17: 12
1. Kafedra biokhimii I Mioskovskogo ordena Lenina medlitsInskogo insti-
tuta im. I.M. Sechenova.

MARDPSHEVY S.R... prof.
1. ~ j - - ,
Raturai and their b;nl.391-3-1 and
Ve.Ft. ',.!, S"SR n,, / -3r,.-4-' 164- (,,111 RA 18, 8)
.~ N "04~ - ~,
1. 'Vitoe-presideut Akademii ntecltsimkikh na-uk S-".'~R.

ILMASHEV, S.R.; UARGORINA, L.1-1-- LESTROVAYA, N.P.; BROKER, T.F.
Amino ac-ld dacarbo~w-
ylases in bacteria of the intestinal group.
Zh. mikrobiol. 40 J1163 (MIM 17-21)
1. Iz Instituta bialogicheskoy i meditsinskoy khimii AMN SSSR
i Instituta epidemiologil i mikrobdologii imeni Gamalei P14N
SSSR.

MARDASH&V, S.R.
Decision of the Centxul Committee of the CPSU and the
Council of Ministers of the U.S.S.R. on "Measures for ftm-
ther progress in biology and strengthening ties with prac-
tical Issues" and the tasks set before the Academy of Medi-
cal Science of the U.S.S.R. Vest. AMN SSSR 18 no.6:69-77
163. (KIRA 17:1)

11 "LlI-SH-PI1,15 3.Tt. (Moskva)
. ~-r .: I - - , ;.mi im
3.ymplmimn or T,he p Pho~dil~lr-e -,Olt~alya* wr;rk
of somi, I-aboratorics of qome an"' Far-5. Vop. irel, ~rlin. 9 no. 33
127-.71' MI-,Te 17-,,-)'

----MA-RDASHEV,..S.R.; VAN SHAO-KHUA [Wang Sbao-hual
Purification of asparaginase from the serum of guinea pigs by
chromatography on a diethylaminoethyleellulose column. Dokl. AN'
W
SSSR 142 no.3:709-712 Ja 162. (MIRA 15:1)
1. Pervyy Moskovskiy meditsinskiy institut im. I.M.Sechenova.
2. Doystvitel'nyy chlen 9VI SSSR (for Mardashev).
(ASPARAGINASE) (CHROMATOGR4WHIC AMALYSIS)

MARDASHEV S.R.; FEOFILOVA, Ye.P.; GALEGOV, G.A.
9
Effect of 13-ciethylaspartic acid on the growth of Escherichla
coll. Mikrobiologita 31 no.3091-395 MY-Je 162. (MIRA 15112)
1. Institut biologichaskoy i meditsinskoy khimii AMR SSSR.
(ESCHERICHIA COLI) (ASPARTIC ACID METABOLISM)

NIKOLAYEV, A.Ya.; MARDASHEV, S.R.
Purification of bacterial asparginase by the carboxyr.,eth7l cellulose
column chromatography. Biokbimiia 27 no.2:330-338 Mr-Ap 162.
(MIRA 15:8)
1. Laboratory of Biochemistry of Nitrogen Metabolism of Microbes,
Institute of Biological and Medical Chemistry, VSoscow.
(ASPARGINASES) (CELLULOSE) (CHROMATOGRAPHIC ANALYSIS)

Ei:rLT,
preparations. ined, khim 8
T,-Ag ~b2.
TI 17 -
Yaf F,(L,-ab4
Lorilria madlts`~nak-;Ogo
linstitu,ta 4mi-rl

MARDASHEV. S.IL; BUROBIN, V.A.
Detection of histivinse in the blood in carbon tetrachloride
poisoning. Vop. med. khim. 8 no.3:320-322 It-Je 162.
WHA 15: 7)
1. Kafedra biokhimii I Moskovskogo ordena Lenina. maditsinskogo
instituta, Moskva.
(CARBON TETRACHLORIDE-TOXICOMry)
(HISTIDASE)

MWASM., -S.- A,.;- MAMEVA, V. V.
----
Purification 6f microbial histidine decarbox7lase. Mikrobiologiia
30 no.3:530-533 My~e 161. (MIRA 15:7)
1. Pervyy moskovskiy meditainskiy institut imeni I. M. E%chenova.
(HISTIDINE DECARBCULASS)
(MICROCOCCACFAE)

SDIINA, L.A.; WiRDASNEV, S.R.
1. ---
Effect of cysteamine on the enzymatic decarboxylization of
amino acids. Biokhimiia 26 no.6:1065-1069 11-D 161. (MIRA 15:6)
1. I;--boratory of the Biochemistry of Microbes, Institute of
Biological and Medical Chemistry, Academy of Mecical Sciences of
the U.S.S.R. 1 Moscow.
(ETIFUIETHIOL) (AMIKO ACIDS) (EvZ11JES)

GALEGOV, G.A.; DFJ30V, S.S.; HAftWHET, S.R.
Synthesis of dl-2-014-0-m--thylaspartic acid and its carbamyl derivative.
Biokhimiia 26 no.5:831-833 3-0 161. (PJU 14:12)
1. Institute of Biological and Medical Chemistry, Academy of M-dical
Sciences of the U.S.S.R. and Chair of Biochemistry, lat Medical
Institute, Moscow. (ASPARTIC ACID)

NIKOIAYEVp A,Y.; MARDASHEVp S.R-.
Imsoluble active acmpound of asparaginase with carboxymethy-
lcellulose. Biolldmiia 26 no-4:641-645 JI-Ag 161. (MIRA 15:6)
1. laboratory of Biochemistry of Nitrogen Metabolism of
Microbes, Institute of Biological and Medical Chemistry,
Academy of Medical Sciences of the USSR, Moscow.
(ASPARIGIMSE)
(GARBacymETHYmELLUIASE)

MARDASHEVt S.R.; SaIINA9 L.A.
Inhibition of enzymatic decarboxylation of amino acids by
DL-penicillamine, L-cysteine and DL-homocystaim. Biokhimiia
26 no. 1:31-39 Ja-F 161. (MIRA 14.2)
1. Institute of Biological and Medical Cherdstry, Academy of
Medical Sciences of the U.S.S.R.9 Moscow*
(VALINE) (CYSTEINE) (AMINO ACIDS) (CARBOXYL GROUP)

DEBOV, S.S.; CHZHAO TUEN-REY;,~VIRDASHEV, S~R.
Biosynthesis of uraci-I by E. coli. Vop. med. khim. 7 no.3:
297-301 MY-Je 161. (I-MU 15:3)
1. Chair of Biological Chemistry, "I.M. Sechenov" First
Moscow Medical Institute.
(EXCIERICHIA COLI)
(UrUCIL)

MAQDA.9RF.V, S. P., and SFXINA. L. A. (US3R)
tiThe Effect of Mercaptoamino Compounds on the Enzymic Der-lrb%-~nxvlatlan
I
or Amino Acids by Microbic Materials."
Re-~)ort p-esented at the .5th International Biochemist-y Congress,
Moscow, 10-16 Aug 1961

MMASM,, Sergey Rufovich;POKROVSKIY, Aleksey Alakoeyevich; PAVIDVA,,
TlBae ~s~, ~KMSHKVA, V. S. . red. ; YEZHOVA, L. L.
tekhn, red,
(Lab4r#.tory demonstrations for lectures on biological chemistry;
manual for teachers] Demonstratsii k lektsiiam po biologicheskoi
kbimii; posobie dlia prepodavatelai. Mosk7a., Gos.izd-vo Wvysshaia
shkola," 1961. 142 P. (KIRA 14:12)
(Biochemistry--.&Udy and teaching)

-MARDASHEV# S.R.; DEBOV, S.S.; YAROVAYA, L.M.
Biosynthesis of orotic acid from aC-ureido-
and aspartic acids. Dokl. All SSSR 134 no-3:713-716 S 960.
(MIRA 13:9)
1. Fervyy Hoskovskiy meditainskiy institut im. I.M. Sechenova.
2. Deystvitellny7 chlen A1411 SSSR (for Mardashev).
(OROTIC ACID) (SUCCUTIC ACID) (ASPARTIC ACID)

LERMU1, H.I.;.H&DASHEV, S.R.
Enzymatic axchange of ammonia and the amide group of f,.-Kato
succiaamic acid. Dokl.hli SSSR 134 ao.2:460-462 3 160.
04MA 13:9)
1. Pervyy Moslcovskiy maditainakiy institut im. I.M.Sechenova.
2. Ueyatvitel'nyy chlen A1411 SSSR (for Mardashev).
(SUCCllU',MIG ACID) (.U#(ONIA) (AHIDASES)

YARD&S CHMO TINY-Rff
___ LI ~~~ ~-*
Inhibition of transamination by cystaine in the rat liver.
DokLAH SSSR 133 no-1:230-232 J1 16o. (RDA 13:701
1. Pervyy moskovski3r maditainskiy institut imeal I.H.
Sechanova. 2. De7stvitel'W chlan PLIU1 SSSR (for Mardashav).
(AMINO ACID MgT&BOLISH)
(CYSTRIN3)

LEW,, H.I.;,M&FJWREVi S.R.
Studying the biasynthesis of asparagine by the use of labelled
prepursors. Biokhimiia 25 no.5:946-953 S-0 1600 (MIRA -14:1)
1. Chair of Biochemiswq FAtst Medical Institute, Moscow.
(ASPARAGINE)

LF&M $ M. L; IWMASHEV,_ S. R.
I/
Synthesis of $-amide of 4-C t-af-ketosuccinic acid. Biokhimiia
25 no.4*.701-704 -Tl-ACr 160. (MIRA 13:11)
1, Chair of BiochemiotFy2 the lot ~Wical Institute, Moscow.
(AMIDES) (CULACETIC ACID)

LESTROVAYAp N.N.; MARDASHEV, S.R.
Effect of certain halogen derivatives of phonylalanine on decarbqxr-
lases in Straptococcus faecalls. BiolkhImils, 25 no.2:227-232 YX-Ap-
f6O, (MIPA 14:5)
1. Laboratoriya biokhIndi mikrobov Instituts, biologicheskoy I
meditsinakoy.khimii Akademii meditsinskikh nauk SS-SR, Moskva.
(AIAIIINE) (DECARBCKYIASES)
(STHErTOCOCCUS FAECALIS)

14MASBEV9 S,R.;- DEBOV, S.S.; FEOFILOVA, E.P.
Bacteriostatic effects of 5-bromo-6-hydroxypyrimidiz.--. Vop. mad.
khim. 6 no. 6:61,3-644 N-D l6o. (KM 14:4)
1. Kafedra biokhimii I Moskovskogo meditsinskogo instituta imeni
I.M. Sechenova i laboratoriya biokhimil mikrobov Instituta
biologichesk i med:Ltsinskoy k*himii AMN SSSRj Moskva.
(V4MDINE) (MYCOBACTERIUM) (F.SCIMRICHIA COLI)

7RAR'qKIY. Boria Illich (deceased]; IVANOV. Illya Illich; MMMASH3v,
-Sergey Rufovich; DEBOV, B.S., red.; B7AL'CHIKOVA,- ~V.S.,
tekha.red.
(Biological chemistry] Biologicheakais khimiia. Izd.3., iapr.
i dop. Moskva, Gos.izd-vo med.lit-ry, 1960. 489 p.
(KIRA 13:9)
(BIOCHEMISPRY)

17(3)
AUTHORS: Mardank SOV120-59-124-2-60171
QX,23. R. Member
An USSR
S
i
,
em
na, L. A.
,
TITLE: The Effect of Penicillin Amine Upon Decarboxylation of Amino Acids
by Microbial Preparations (Vliyaniye penitsillamina na dekarboksil-
irovaniye aminokislot mikrobnymi preparatami)
PERIODICAL: Doklady Akademii nauk SSSR, 1959, Vol 124, Nr 2, Pp 456-458 (USSR)
ABSTRACT: By adding L-penicillin amine to the aminopherase system of the
liver the enzymatic activity is suppressed in vitro. Penicillin
amine is said (according to Ref 1) to form with phosphopyridoxal
a thiazolidine derivative. On the basis of this fact it ma
b
e
y
assumed that penicillin amine will hamper those reactions which
take place under the participation of phosphopyridoxal enzyMe3.
In fact, DL-penicillin amine considerably suppresses D-serine
dehydrogenase of N. crassa and Escherichia coli (Ref 2). In this
connection the solution of the problem mentioned in the title
a
w
s
interesting. The authors investigated the action of penicillin
amine in amino acid decarboxylasee of 1) E. coli (arginine decarbo
-
xylase); 2) B. cadaveris (lysine decarboxylase); 3) Micrococcus
sp.n. (histidine decarboxylase); 4) Cl. Welchii SR 12 (glutamine

Ca
/~
d 1/ decarboxylase); 5) S. faecalis (tyrosine decarboxylase); and
6
r
- ) Pseudomycobacterium sp.n. (aspartico decarboxylase),(Ref 3).

SOV/20-59-124-2-60/71
in Amine Upon Decarboxylation of Amino Acids by Yicrobi,l
The Effect Of Fenicill -2 -3
Preparations DL-penicillin amine was added in concentrations Of 10 1 1 9
id was then
and 10-4 mol/liter. An M/60 solution of the amino ac ution, and the
added to the enzymatic preparation in the buffer sol
ation was determined in the vlarburg apparatus,
rate of decarboxyl nicillin amine on t e decarboxylation
Table I shows the effect Of pe on of 10- mol/liter con-
of lysine of B. cadaveris. A concentrati -4
s, while this effect is weak at 10
siderably hampers this PrOces g effect can be clearly observed in
mol/liter. The same 9uppressin rkers (Refs 2,4)
arginine decarbOxYlase (E.Coli). Snell and his cO-wO
ral phosphopyridoxal ferments need metal ions
maintain that seve ivation. In order to check that statement the
for a complete act 2+ investigated in the above
effect of A13+, Za 2+, Fe3+, and Cu was
process of E.coli. The results are summarized in tabled 3 and 4
f Al, Fe, Cu or Zn ions does not
They show that the addition 0 by penicillin
resqiOl'l of decarboxylase reaction
eliminate the SUPP nd 5 referenceag 1 of which is Soviet-
amine.- There are 4 tables a
Card 2/0

MDAMV, S.R.; LU ZHU-MH (Lu Ju-sharg); ROHAMDV, Tu.A.
Synthesis of acetylaspartic acid. Mlkrobiologita 28 no-5:641-646
S-O 159. (MIFLA 13 -.2 )
1. 1-y Koskovakiy ordena Lenina meditainakiy inctitut im. I.M.
Sechenova.
(ASPARTIC ACID rel.cpda.)
(CLOSTRIDIUM metab.)

ORMOVICH, V-N-, D-rof.; MAJMkSIOV, S.R., prof.; IMBOV, S-S., kand.med.nauk.
Soviet biochemi-M-4-rsit the U.S.A. VestbW SSO 14 no.7:
57-67 '59. (MIRA 12:9)
1. Daystvitellnyye chleny AM SSSR (for Orakhovich, Debov).
(MUTED STATES-BIOCHMISTRY)

OREMOVICH, V.N.; BYCHX07. S.M.; DEBOY, S.S.; RARDASIMV, S.R.; SSVF2IN, S.Te.
Second International Congress on Clinical Uhemistr-,r. Vest.AMN SSSR
13 no.2:62-74 158. (KIRA 11:3)
(CIMMISTRY, 14EDICAL AND PRARKAGEUTICAL)

MARDASHEV. 5.R.; LU ZHU-SHAN [In Ju-shang]
Microbial amino acid D( -amidasee [wich ell-g-ar7 in gaglishl.
Biokhimila 22 no.1/2:369-374 Ja-Y '57- OCOA 10:7)
1. Irafedra biologichaskoy khimii
institute in. I.M.Sechanova.
(CLOSTRIDIUM.
cadavoris. amino acid
(MICROCOCCUS. metabolism.
amino acid 0(-amidase
(AHIDASES,
amino acid 0( -amidase
Hicroccosus (Rua))
1-go Moskovskogo maditsinakago
C(-amidass (Rua))
(Rua))
in Clostrilium cadaveris &

-~ ~-- M A RDA ~ I i E V, S -
SEVERIN. S.Ya.; KOD**V, S.R.; BUCHKOV, S.M.; DEBOV. S.S.
International Congress on Clinical Chemistry. Vop.med.khim. 3 n0.5:
397-400 S-0 157- (MIRA 10:12)
(CHPIMISTRT, MEDICAL AND PHARMACEUTICAL)

USTROTAYA. M. ff. ; K&OASHZV, S.R.
Synthesis of phonylalanine and tyrosine peptides by chymotrypsine.
Wop.medokhim. 2 no.4:294-"8 ii-Ag 156. WRA 9:10)
1. Fafedra biokhimil I Hoskovskogo ordena Lanina maditainskogo
inatituta imeat I.H.Sechanova.
(PROTRASESO
chymotrypeta,.effe on peptides & tyrosine synthesis
in vitro (RUB))
(PEPTIDES*
synthesis in vitro. eff. of chymotrypain (Rua))
(TYROSINE,
same)

it !~Rd
'
,
-aaLmd
la th
rganEs S R~ Uardashev Us,6ekhi
Md
tharat
.
_T iivk, r vitli~' 7refec~jx~ the fouawf4 gc~eral
Ai an
ts
f
f ottalti;* ~2) biol
iynthtsis;- (3) enzymk dmnit'da
.
'(5y
d cx&etkn of"NIH
tWm i3f_arnldO- (4) t6nuatiort an
.,

Id ...
-of otfuzr s6staticri. (7):am eg- - -
es~ut, bk
amifles Im
tuh-je of

77777777

jr

Ell" A" IV E A9 4 14 t 19 mi

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q-

musael7t"I.
Eye it
M=fi:cWvi -(Lst Moscow Wed.-
sh F~
Cr
,
i~4
.=d th hart*rtm*.W and
Ril vmm dempita
- f
~itd Lvtw b6id
hvim,' list peifiioAht Oqsue

MAW
t ttmovcA - the re9duc cut loto ta wit 194~42
& min-imkWirinirBleudonc. the: fiz~dhomwiwicft-j~
For -'s
,
ws- f &Ud - usae-lissue per. n2l
3w
-
-
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-
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is
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thie i(n&itilule-
:phospbatc to the butated isi=ibmcs rabea-
o thaid-the
synthesizinc idivity imt dt6vt equat t
homo* nate~:. The.tiuclcar- lraeffi5a- Eui&,MP;r~t. fluic.
r
tWki
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-33.

PLKWZ.K.I.; KARDASIMV.S.R.; KULAKOVSKATA
Certain A'--derivatives of amino acids and of paptides. Zhur.ob.
khim. 25 no.2:3?1-374 F 155. OCIRA 8:6)
1. 1-y Hookovskiy meditsinskiy institut
(Amino acids) (Peptides)

- B~r'is"Illich Zbarskiy IM-1778
Card 1/1 Pub 122-9/9
Author : Mardashev, S - R., Cor Wmb Acad 'Hed Sci USSR
Title : Boris Il'ich Zbarskiy
Periodical : Vest. ANN SSSR, 1, 62-63, Jan/Mar 1955
Abstract : Boris Il'ich Zbarskiy, Soviet biochemist, died suddenly on October 7, 1954
at the age of 70. He was an active member of the AW USSR and P member of
the CPSU. He was recipient of many awards. He was an excellent teacher eand
taught biochemistry in the 1st pedagogical institute of NARKOMPROS and in _Ist-
and in 2nd Ybscow medical institutes. His name is associated with foundin.-
of the physico-chemical institute imeni Karpov and of the biochemical insti-
tute of NARK012DRAV. He was the founder and the first head of the institute
of nutrition. B. I. Zbarskiy was born in 1885 in Kamenets-Podol'sk where he
received his secondary educati6n. He received his chemical training in
University of Geneva and passed a qualIfying examination at the University of
Peterburg, Together with V. P. Vorobyev he embalmed Lenin's body in 1924.
Institution:
Submitted :

,V /~~? 511s- v ~:;- 4--
ZBARSKIY. B.I.; ITANOT, I.I.; MARWHIV, S.R.; UPLAKSKIY. S.Ya., re-
daktor; BOBROU, U.N.. Ukftftdliiik*~~sdaktor.
[Biochemistry] Biologicheakala khInila. 2-s tzd. Koakva, Goo.
izd-vo mod. lit-ry, 1954. 618 p. [Xicrofilm] (MYRA 7:11)
(Biochemistry)
.r-

GIAWOTA, V.N.,W1RDASHEVg S.R..;SZOTVA, L.A.
-
New microorganiso coataining decarboxylase of )-histidlne. Mikro-
biologita. Moskva 22 no.2:141-144 Mar-Apr 1953. (GLHL 25:4)
1. Pirst Moscow Order of Lenin Medical Institute.

7.2z__ &:-

=s R UMMIM

reacm With-tionaamino aci&, through but 1.4
CHO md. 1. 911% group. - Thermc6iii occu
steps thraugfi~ formation of a calorlez -compotiad I of

`
H IR
_-
Eck tPeli asses
N. CHO (H). Wh p
ftiw
'whl'~
13 cyclk product
IfQk&g. CIfdH(0H efn)
,
.
is stuble. The colodass intermediate fi de5troyed by Nffr.
OR semicarbazide
with formatiarl'of
;4

e
~th oorresfionding I deriv. and liberat (oil of th~ amLw acid
R
eaction: of sa%alf.-I Wi
th'arn [no acitia procted best in aq.
'
'
t
I ith: excm I atAbout 0
ne urn w
d
.
- To 2 g. 11,NCITSCOAFf
ill fill Ir'O W" adtied Tvith-I'm ~Goling 3 rill. 385 ak'T
^d
1111ft. the iota. Wa treitc-d with'60-70 W.abs MeOH and

040 mt. rbs. llt'~%-yieldfrlg 10% a. thN. was takerL up la
ujo U-tat'-d with (Cozuh to remove, the: admixed Ca. silt

ter a
Adorr. acid contair.InKlit present iii Pam ad
aratmpptd-WithEtto-Meoll. II(R ff ob
'is td.VTM at-S. _qeC0 aljdrEt-O zhil, r in -racull,
MG.4as idded with cool-
r (nelitrahled is above), =led I fir. longer,
tug 4e
tal ug.
,
thm kcf;t it roam temp., then treated with ?kfeQff
-light blue plit.,ofAlit Cu~drriv Ci 0
F-40 yielding. V
3olti
6f It (R m 10 Ott it
Heating the 4
.-.
q.
estlince.,gava4f6l Ulm ormroa-
sLeam bath uatil CHO t
No SL Ppt~ a ur (P - 1h, Wle

11(rt -.Yo) prepd, SiMC fro
in in
-11 in d6d Or haSk CnMi-
hydrate ting aq, 1011M. Of
-of In, jvhid
Writ ;;14ts ill formatlon I wll~ followed sp,,c
_
'
i

4otorattrically: ~, the cofvei of
trop
m~ction
rogrw art
*
'
p
shown..
- Eketroli-iiii n4tictlot.: of Ul
esul ed in no reduo~
rt
tiou Ott the rwh6dd -fno ccjlar lo4s):whilt at: &ze anode the
-d ta KN '$,1l.
ted waivxilit, trCH-.COJE and 11COU

PARDASM, S.R. I KULAKOVSKAYAp IT.A.
Codecarboxylase of the aspertic acid. Top.med.khiu. 4:231-zJ6 152.
(mIRA 11:4)
1. K3fedra biakhimii I Moskovskago ordena lenina meditainskogo
inatitutas
(COWAnOXYLAZE) (ASPARTIC AGM)

Synthesis and by a of tfuuthjinie In
gTowths. X14!Iftev and A. K. Pikkat -41VIT-W13,
I kid Vaig"i -YN-9 78,745-s(IM) - 1`118VIAliC ACtiVitY
ith frgpmt
'~~tO HoUp, exc;~~tWtcd'by the Cluts-
hUme niol, was detd. In sarcoutas as vueh and in the livfft
4 mmor-hr4ring rate. Synthetic aictivity wAs shown In
Of I U,UM-hCJTM. AU41 Only In 30C' Of t1Of1HAI ASIfinals;
1101"Mic activity was shown by 411-allInUN (liver Ali"
The rate of synthesis was mitch hishcr in lunkw.
licArefs, and the hydrolysis rate a little higher. The
turmir 6-mce Itself showed no ife vilro synthetic xctivitv and
it* hydrolytic Activity wo linvi-T thals norimil, but 1hi* III-
cTe.i.wil with development of the tuntor. The 247tUll gtUtA-
th"ir level In the liver of at tunuit4x-Am was above normal,
while In the turner the L-vci was lower than In the Lives but
several flums higher than its mulcte or its Connective tissues
andskin. G. W KosoUixiff

MARDASH91, S. P-
USSR/Chemistry (Biological) 21 May 51
Transamidation
'"Biological Synthesis of Asparagine and Glutamine
,by Transamidation," S. P. Mardashev, N. N~
Lestrovaya
."Dok Ak Hauk SSSR" Vol LXXVIII, No 3, PP 547-550
Showed in expts with rat liver sections that gluta-
mine is synthesized from glutamic acid and aspara-
gine (both at alkaline and acidic reactions) and
that asparagine is synthesized from aspartic acid
and glutiamine (at acidic reaction only).
18M6

HARDASHEV, S.R.
EffOCt Of SOMe DOlypePtides on the sugar contents of blood. Vcn.~ed.
khim,. 3:263-274 '51. (MIRA 11:4)
1. Kafedra biokhimii 1-go Hoskovskogo ordena LeninA meditainskogo
inatituta. . . . :
(BIDOD SUGAR) (PEPTMES)

ZBARMT, B.T.; ITARDY, I.I.: KARDASM, SJL; SHIRHDVA, L.G..
'T'M~
redaktor; KARASIK, M.P., tex c~i ~-redajrtor
[Biological chemistry] Biologichaskala khImila. Hookwa, (;os.
izd-vo meditsinakol lit-ry. 1951. 611 p. (MT.RA 8:10)
(Biochemistry)

CP
'=41" '7Lf ad S.
d L. V=*Ina 3171"'AC,4j. 'N'tlik
SSS.'R' f4, A37-44)(1950).-Incubation 0 rat-liver 11-ri '
ntens I hr. aIMPInOom No with wim of clyntalic acid wilh
addn. of either millarmiclue, mpastic mcm, NUM. glutamine,
or glutandc acid In pho%phale buffers (Plf 0 of 8). followed
by p2rfiliao c1rotnatography .1 the products showed he
synthesis of glycine from glyoWic acid, which proceeds at
pit 0 or 8 bath In wahic and anaerohic conditions. Since
addn. of Nile salts does not Increase the rate, the reactim is
not limply a reversed deamination afglycine. Thearderof
effectiveness In the synthesis Is given by the ascending series:
oupartic: ", gfutamic ". aspatagine. Stutamine. Vi-
rect transamination is a possible course, and po"ibly 2.
enzymes participate, cauiing mWensation of the anvido
group with carbonyl of glyoxalic acid, followed Ivy reduction
and hydrolysis into glyrine and aminodicarboxylic acid.
G. M. Kosal2poff
1114

C-A
R. Nixtdobev and L. A~ 14emirtia. Pokk4y Ak,vd
.351 A(IMM-Cattle liver (3 Lit.)
nascrtated In Rao at rem" temp , freed CA Protein bv'21411,
OXCUNII. filtered (local Val. lit.). Cod. with FW(ofr-
I
nolve throme nt frorm X1. filtratir, "McIl. in mrat, at 44",
n
1-mvilucrAl. rotated 44141 atfut Acidifictl with hl'~
'641,ank,"l by arid In V;, jI*FA , I-
fugent. treed at( ph"Ificatatoptatte iqam Over" lay 4ccelint,"'
forml of "a lay 1101;o. cfrtcal. at 40" to 44110 mi.' tuate ativ
with 112(oll),snaltlild. with 3 Vaal.. !ftlc~ Moll tom"'We
(Z dictarloo,xytie .I.. retmer"I with
,,-k,1- Ito 3"0 ent. afoul 4-1y ppid. bv :M". lIgMAO.
&SVC A PPC (LUVAtOd In 1 (1111KA14011) Watch. Ireatnt W011
HIS. muUnlimcd with Xlfj Cut cmcd. at 40'. gave 64-ifte
tyraosime (retnoved tayfiltestion), continued confine yielded
-tacric, teacide, ad the find concentrate boamught down to
3 ml. and tamated with 4 ad. 911'a R(Off &M chilled. yielded
dtcr N hts, as dotam mass, 44 asgoamatom In 7 mg. ywhi;
the Identity was checked by uAkruictVic examu. atad
mastysis ludk*%ted the meachydraft,
tn. Z:8-70'. The results coniirm the Me 00 asp"&.
. lit.
give in living matter. ( . lit. go-w"Pod

Gooft" of &m"044" fm Foods of 6mbuvktkc UOR(m.
P- IL EtiuV4 w*t N. & Kulakovska" (M-tra.
lt=xG,m,-M, 21
Clow,
SW anxax. &CWS wm at t
Wa. cpc~ of Pwm"Wkr~wft si'd M&W.WmaL Lysina is
Sam mt - is the anattabic- thm the aembk
of dioutaxitk vadaa4cWs i4 (&Wy cm.
stant for 413 ?--" examiaod, in spite of the bict tha m2unts at
IndividuA wniw-seds vuy comklamUy. T14- waftm-add covatit.
atM dam not %VW to br. Wated t* the ca t* docutaxykta
padcuW amua-ocUm~ vAr Is it Woctrd byMilelmt ctature can.
diwas. D, Ic SUVTR.
& n""j urd

CA
New mtdwd (*r tM quiladfAtive dowminatim of amma
dicubilqUe adds and Malt maddes. S. R. NbrilAshev
JAII V. V. NIA1113MA (First Moscow Med.1ust). -Ria.
1*11411" 19, 4wo 721(145(1). --The amitto fficaffmillyfic acick
4"'1 1414111k. W.- ;) W.-Ir U-jul. fri"ll their ;41110C.4
all-Iiimmir) liv mWittilkwe m AlAl, tkil kpl
. ith 1ICI IT. Wul.All.l. C..U 37, CNIP)
A~JiAltir 36d And AqUfAgint- WVfC df,14. Vnglf 6~.AIIV Willi
ICA.
K1UtAMiCACidAMJ e=aMine With bacteriAlglut.tiliv a6l dr.
vArboxyUm (C.A. 4J, 3MU), The 164MV -All. Anti the
,,nur vewl In the WAsburg app. wffe uwl, fir,t. Nt the
&m. tit uturalgine. an4f Own for gtutamine. Argurti-,
mid Itillamic llcktli ucte dod. In diffritnt wwwls. The
-nalesim protein hydrolyzatesand in aninul timucs. Thut,
rAbbit liver contained (in mg. %) asjwACine 3.6. gfutatnin~
aspartic " 21.2. and gfutamic Acid 429 1. The cxw,
responding vahL~ ftw mlkit kulney ware 7A. 21.7, 16.1'.
..nd 75.5, retp. IL ly".0ey