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Wyszukujesz frazę "peptide" wg kryterium: Temat


Tytuł:
1,3-OXAZOLIDIN-5-ONES DERIVED FROM PROLINE AS CHIRAL COMPONENTS IN THE SYNTHESIS OF PREDICTIVE ENANTIOSELECTIVE COUPLING REAGENTS
Autorzy:
Kasperowicz-Frankowska, Katarzyna
Kolesińska, Beata
Gzik, Anna
Jastrząbek, Konrad
Kaminski, Zbigniew J.
Powiązania:
https://bibliotekanauki.pl/articles/895643.pdf
Data publikacji:
2018-08-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
enantioselective condensation
peptide synthesis
chirality transfer on nitrogen
chiral nitrogen atom
triazine coupling reagent
Opis:
1,3-Oxazolidin-5-ones derived from both enantiomers of proline and trichloroacetaldehyde were prepared and applied as amine component in the synthesis of chiral predictive triazine based coupling reagents. The usefulness of these reagents in the condensations yielding enantiomerically enriched products from racemic substrates was presented.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 4; 921-927
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A brief overview of the process of the elucidation of GnRH structure (1971)
Autorzy:
Kochman, K.
Powiązania:
https://bibliotekanauki.pl/articles/80024.pdf
Data publikacji:
2012
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
luteinizing hormone
follicle stimulating hormone
receptor protein
protein G
cell membrane
hypothalamic peptide
adrenocorticotrophin
radioimmunoassay
central nervous system
gonadotrophin releasing hormone
receptor
neuroendocrinology
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2012, 93, 4
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A novel cis-peptide bond motif inducing β-turn type VI. The synthesis of enkephalin analogues modified with 4-aminopyroglutamic acid.
Autorzy:
Kaczmarek, Krzysztof
Kaleta, Maciej
Chung, Nga
Schiller, Peter
Zabrocki, Janusz
Powiązania:
https://bibliotekanauki.pl/articles/1044069.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
constrained enkephalin analogues
4-aminopyroglutamic acid
cis-peptide bond
β-turn mimetic
Opis:
A new pathway leading to a mixture of four isomers of 4-aminopyroglutamic acid is described. Michael type addition of Z-ΔAla-OMe to enolates prepared from acylaminomalonates, followed by hydrolysis and decarboxylation give protected 4-aminopyroglutamic acid with the 4-aminopyroglutamic acid with the cis:trans ratio approximately 3:2. This mixture was incorporated into Leu-enkephalin (position 2-3). After separation of peptides it appeared that all analogues were essentially inactive in guinea pig ileum and mouse vas deferens bioassays.
Źródło:
Acta Biochimica Polonica; 2001, 48, 4; 1159-1163
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Actions of several substituted short analogues of porcine galanin on isolated rat fundus strips: a structure-activity relationship
Autorzy:
Korolkiewicz, R.P.
Konstanski, Z.
Rekowski, P.
Ruczynski, J.
Szyk, A.
Grzybowska, M.
Korolkiewicz, K.Z.
Petrusewicz, J.
Powiązania:
https://bibliotekanauki.pl/articles/71045.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Fizjologiczne
Tematy:
gastric fundus
genitourinary tract
peptide
gut
peripheral nervous system
endocrine system
amino acid
smooth muscle
rat
Źródło:
Journal of Physiology and Pharmacology; 2001, 52, 1
0867-5910
Pojawia się w:
Journal of Physiology and Pharmacology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Aminokwasy, glikany, peptydy i białka w ścieżkach diagnostycznych i terapeutycznych chorób cywilizacyjnych XXI wieku : projektowanie i charakterystyka fizykochemiczna oraz strukturalna
Amino acids, glycans, peptides and proteins in the diagnostic and therapeutic pathways of the 21st century civilization diseases : design, physicochemical and structural characterisation
Autorzy:
Bylińska, Irena
Dzierżyńska, Maria
Giżyńska, Małgorzata
Guzow, Katarzyna
Jankowska, Elżbieta
Jurczak, Przemysław
Kaczyński, Zbigniew
Karska, Natalia
Kowalczyk, Agnieszka
Kuncewicz, Katarzyna
Orlikowska, Marta
Sawicka, Justyna
Spodzieja, Marta
Szpakowska, Nikola
Szymańska, Aneta
Wieczerzak, Ewa
Witkowska, Julia
Rodziewicz-Motowidło, Sylwia
Powiązania:
https://bibliotekanauki.pl/articles/2200549.pdf
Data publikacji:
2022
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
fluorophores
fluorescence spectroscopy
antimicrobial activity
anticancer activity
Cystapep
Stahylococcus aureus
antimicrobial compounds
amyloidogenic protein
mutagenesis
fibrilization
proteasome
aging
neurodegeneration
self-assembling peptides
tissue engineering
biomaterials
immune checkpoints
peptide inhibitors
immunotherapy
ligands of TAP protein
viral diseases
NMR structure of the UL49.5 protein
glycans
glycoconjugates
fluorofory
spektroskopia fluorescencyjna
aktywność przeciwdrobnoustrojowa
aktywność antynowotworowa
Staphylococcus aureus
związki przeciwbakteryjne
białko amyloidogenne
mutageneza
fibrylizacja
proteasom
procesy starzeniowe
neurodegeneracja
peptydy samoorganizujące
inżynieria tkankowa
biomateriały
punkty kontrolne układu immunologicznego
inhibitory peptydowe
immunoterapia
ligandy białka TAP
choroby wirusowe,
struktura NMR białka UL49.5
glikany
glikokoniugaty
Opis:
The civilization diseases of the 21st century are non-infectious disorders, affecting a large part of modern society. They are associated with the significant development of industry and technology, and hence with environmental pollution and an unhealthy lifestyle. These factors have led to the development of many civilization diseases, which currently include: cardiovascular diseases, respiratory diseases, diabetes, obesity, malignant tumors, gastrointestinal diseases, mental disorders and allergic diseases. The development of technologies, including modern therapies and new drugs, resulted in increase in life expectancy. This creates a global problem of an aging population with an increasing number of diseases of the old age, i.e. dementias. In addition, sedentary lifestyles and changing diets are the reasons why more and more people develop metabolic diseases, as well as neurological and cognitive disorders characterized by progressive damage to nerve cells and dementia. Currently, problem on a global scale is also the growing resistance to existing antimicrobial drugs. Therefore, the scientists face many challenges related to searching for the causes of these diseases, their diagnosis and treatment. Scientific research conducted at the Department of Biomedical Chemistry at the Faculty of Chemistry of the University of Gdańsk is part of this research trend. In this publication, we discuss various research topics with the long-term aim of solving the problems associated with the diseases mentioned above. The following chapters are dedicated to (i) looking for new effective fluorophores with diagnostic and anti-cancer activity; (ii) designing of new compounds with antibacterial and antiviral activity and their synthesis; (iii) investigating the mechanisms of amyloid deposit formation by human cystatin C and possibilities of inhibition of this process; (iv) designing and studies of compounds activating the proteasome with the potential to suppress the development of neurodegenerative diseases; (v) designing peptide fibrils and hydrogels as drug carriers; (vi) searching for peptide inhibitors of immune checkpoint as potential drugs for immunotherapy; (vii) studying the mechanism of action of selected herpesviruses by determining the structure of viral proteins and (viii) studying the composition of natural glycans and glycoconjugates in order to better understand the mechanisms of interaction of bacteria with the environment or with the host.
Źródło:
Wiadomości Chemiczne; 2022, 76, 5-6; 393--431
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Anti-pathogenic properties of plant peptide hormone phytosulfokines [PSKs] and its selected analogues
Autorzy:
Bahyrycz, A.
Saniewska, A.
Konopinska, D.
Powiązania:
https://bibliotekanauki.pl/articles/55358.pdf
Data publikacji:
2008
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
antipathogenic property
Botrytis tulipae
antifungal activity
Phoma narcissi
phytosulphokine-alpha
plant peptide hormone
phytosulphokine-beta analogue
Opis:

Phytosulfokine-α (PSK-α) (H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-Gln- OH) (I), a sulfated growth factor universally found in both monocotyledons and dicotyledons, strongly promotes proliferation of plant cells in culture. The C-terminal truncated analog named PSK-β (Tyr(SO3H)-Ile-Tyr(SO3H)-Thr) (II) showed a 10-fold lower activity than that of the parent pentapeptide. Because PSK-α promotes proliferation and differentiation during the plant growth we undertook the studies on the influence of PSK-α on plant defense mechanisms in that period. In present studies on PSK-α (I), PSK-β (II), and its analogues, we performed a search of another biological properties. The aim of our investigation was evaluation of PSK-α, PSK-β and their selected analogues in relation to growth and development of plant pathogens, such as Phoma narcissi and Botrytis tulipae. In these studies we elaborated the synthesis of PSK-α or PSK-β and their 22 analogues modified by natural and non-natural amino acid residues. Peptides were synthesized by the solid phase method according to the Fmoc procedure on a Wang-resin. Free peptides were released from the resin by 95% TFA in the presence of EDT. Biological effect of these peptides was evaluated by test on the growth and development of pathogens of P. narcissi and B. tulipae.

Źródło:
Pestycydy; 2008, 1-2; 109-117
0208-8703
Pojawia się w:
Pestycydy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Antibacterial peptides of the moth Galleria mellonella
Autorzy:
Mak, Paweł
Chmiel, Dorota
Gacek, Grzegorz
Powiązania:
https://bibliotekanauki.pl/articles/1044082.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
antibacterial peptide
bacteriocin
insect immunity
hemolymph
cecropin
Opis:
The work describes purification and biochemical characterization of two inducible antimicrobial peptides from the hemolymph of Galleria mellonella. The peptides were isolated by a sequence of reversed-phase chromatography steps from the hemolymph of larvae immunized with viable bacteria. The first peptide is a member of the cecropin family while the second one is rich in proline residues and has a unique sequence.
Źródło:
Acta Biochimica Polonica; 2001, 48, 4; 1191-1195
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Antinociceptive effect of MAS MT in rats
Autorzy:
Rykaczewska-Czerwinska, M.
Radosz, A.
Szymanowska-Dziubasik, K.
Konopinska, D.
Plech, A.
Powiązania:
https://bibliotekanauki.pl/articles/55342.pdf
Data publikacji:
2008
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
Tenebrio molitor
antinociceptive effect
rat
larva
brain
neuropeptide
insect neuropeptide
Manduca sexta
proctolin
myotropin
biological activity
peptide chain
peptide
Opis:
MAS MT is a myotropic decapeptide isolated from Manduca sexta. This peptide exerts stimulatory effect on insects heart-beat frequency. The present study was undertaken in order to determine a probable antinociceptive effect in rats of native synthetic decapeptide, MAS MT-I and its two analogs, heptapeptides MAS MT-II and MAS MT-III. All these peptides were applied directly into the lateral brain ventricle (icv) at three doses: 10, 25 and 50 nmol. The analgesic (antinociceptive) effect was evaluated by a tail immersion test. It was found that two doses of MAS MT-I: 25 and 50 nmol induced significant antinociceptive effect, while MAS MT-II and MAS MT-III exert a less antinociceptive effect in comparison with native MAS MT-I. Prior icv administration of naloxone, an opioid antagonist weakly blocked MAS MT-I effect. We conclude that antinociceptive effect of MAS MT-I in rats is not mediated by central opioid system.
Źródło:
Pestycydy; 2008, 3-4; 139-146
0208-8703
Pojawia się w:
Pestycydy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Antioxidant Activity of Hybrid Sturgeon (Huso dauricus × Acipenser schrenckii) Protein Hydrolysate Prepared Using Bromelain, Its Fractions and Purified Peptides
Autorzy:
Noman, Anwar
Wang, Yuxia
Zhang, Chao
Abed, Sherif M.
Powiązania:
https://bibliotekanauki.pl/articles/2019350.pdf
Data publikacji:
2022-03-01
Wydawca:
Instytut Rozrodu Zwierząt i Badań Żywności Polskiej Akademii Nauk w Olsztynie
Tematy:
hybrid sturgeon
enzymatic hydrolysis
hydrolysis optimization
bromelain
degree of hydrolysis
radical scavenging activity
peptide purification
Opis:
Protein hydrolysates could be a natural and safer source of antioxidant peptides. The purpose of this study was to optimize the hydrolysis of Huso dauricus × Acipenser schrenckii sturgeon proteins using bromelain and purify antioxidant peptides from hydrolysate. The degree of hydrolysis of 18.69% was obtained under the optimal conditions and hydrolysate had 94.76% solubility, 902 nm particle size and high antioxidant activity. The IC50 for DPPH• and ABTS•+ scavenging activity were 3.14 and 3.81 mg/mL, respectively. The fraction of hydrolysate with a molecular weight of <1 kDa exhibited the highest antiradical activity against DPPH• with IC50 of 2.10 mg/mL. In turn, the IC50 of the most active fraction after the Sephadex G-15 separation was 1.77 mg/mL. The reverse phase high performance liquid chromatography (RP-HPLC) was used to purify the peptides from this fraction. The peptide with histidine, leucine and glycine (MW of 0.2955 kDa) exhibited the highest antioxidant activity (IC50 of 1.33 mg/mL). The obtained fractions and peptides with antioxidant activity could be used as natural substitutes for synthetic antioxidants, especially in food and pharmaceuticals.
Źródło:
Polish Journal of Food and Nutrition Sciences; 2022, 72, 1; 79-89
1230-0322
2083-6007
Pojawia się w:
Polish Journal of Food and Nutrition Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Antybiotyki peptydowe i ich kompleksy z jonami metali
Peptide antibiotics and their complexes with metal ions
Autorzy:
Stokowa-Sołtys, K.
Powiązania:
https://bibliotekanauki.pl/articles/171960.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
antybiotyki peptydowe
metaloantybiotyki
kompleksy jonów metali
peptide antibiotics
metalloantibiotic
metal ion complexes
Opis:
Metal ions are essential for numerous antibiotics. They play a crucial role in the mechanism of action and may be involved in specific interactions with cell membrane or target molecules, such as: proteins and nucleic acids. Due to the fact that complexes usually poses a higher positive charge than free ligands, they might interact more tightly with DNA and RNA molecules. However, complexes may also form during antimicrobial agents application, because a lot of them possess functional groups which can bind metal ions present in physiological fluids. Many recent studies support a hypothesis that drugs may alter the serum metal ions concentration. Moreover, it has been shown that numerous complexes with antibiotics can cause DNA degradation, e.g. bleomycin which form stable complexes with redox metal ions and split the nucleic acids chain via the free radicals mechanism. Therefore, it is widely used in cancer therapy.
Źródło:
Wiadomości Chemiczne; 2018, 72, 7-8; 497-522
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of gel filtration for rapeseed peptides analysis. Short report
Autorzy:
Amarowicz, R.
Kmita-Glazewska, H.
Powiązania:
https://bibliotekanauki.pl/articles/1372750.pdf
Data publikacji:
1995
Wydawca:
Instytut Rozrodu Zwierząt i Badań Żywności Polskiej Akademii Nauk w Olsztynie
Tematy:
gel filtration
peptide fraction
peptide separation
peptide
peptide extraction
food
chromatographic analysis
rapeseed
Źródło:
Polish Journal of Food and Nutrition Sciences; 1995, 04, 1; 88-92
1230-0322
2083-6007
Pojawia się w:
Polish Journal of Food and Nutrition Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Badanie struktury i dynamiki N-terminalnych sekwencji dermorfiny i ich analogów z wykorzystaniem spektroskopii NMR w ciele stałym i rentgenografii
Studies on the structure and dynamics of N-terminal sequences of dermorphin and their analogs by means of solid state NMR spectroscopy and XRD
Autorzy:
Trzeciak-Karlikowska, K.
Powiązania:
https://bibliotekanauki.pl/articles/171648.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
peptydy opioidowe
oddziaływania CH-pi
dynamika molekularna
oddziaływanie peptyd–fosfolipid
spektroskopia NMR
1H Ultra Fast MAS NMR
PISEMA MAS
PILGRIM
XRD
opioid peptides
CH-pi interactions
molecular dynamics
peptide–phospholipid interaction
NMR spectroscopy
Opis:
Deltorphin I (Tyr-d-Ala-Phe-Asp-Val-Val-Gly-NH_2) and dermorphin (Tyr-d-Ala-Phe- -Gly-Tyr-Pro-Ser-NH_2) are natural opioid peptides that have been isolated from the skin of South American frogs [1]. The presence of d-amino acid is crucial for their biological activity. The synthetic analogs of given heptapeptides containing l-alanine are not analgesics [2]. Analysis of the influence of stereochemistry on molecular packing, dynamics and biological functions of neuropeptides is still important for receptor studies and practical applications (e.g. design of new selective pain killers). Presented research is focused on the structure and dynamics of two N-terminal sequences of dermorphin: tripeptide Tyr-d-Ala-Phe 1, tetrapeptide Tyr-D-Ala-Phe-Gly 2, and their analogs with l-alanine: Tyr-Ala-Phe 3 and Tyr-Ala-Phe-Gly 4, using solid state NMR and X-ray diffraction. This study clearly demonstrates that 1 and 2 crystallized under different conditions to form exclusively one structure [3, 4]. In contrast, tripeptide and tetrapeptide with l-Ala in the sequence very easily form different crystal modifications. Tyr-Ala-Phe 3 crystallizes into two forms: 3a and 3b [5], while Tyr-Ala-Phe-Gly 4 gives three modifications: 4a, 4b and 4c [4]. It seems that one of the factors, which can be important in the preorganization mechanism anticipating the formation of crystals, is the intramolecular CH-đ interaction between aromatic rings of tyrosine and/or phenylalanine and the methyl group of alanine. Such interaction is possible only for d-Ala residue. For l-Ala in the peptide sequence, the methyl group is aligned on the opposite side with respect at least to one of the aromatic groups. It can be further speculated that such internal CH-π contacts can also occur during the interaction of ligand–receptor, making the message sequence of opioid peptides more rigid and finally selective. By employing different NMR experiments (e.g. PISEMA MAS and PILGRIM) it was proven that the main skeleton of analyzed peptides is rigid, whereas significant differences in the molecular motion of the aromatic residues were observed [4, 6]. Solid state 2H NMR spectroscopy of samples with deuterium labeled aromatic rings: Tyrd4-d-Ala-Phe 5, Tyr-d-Ala-Phed5 6, Tyrd4-Ala-Phe 7, Tyr-Ala-Phe^d5 8 was used to analyze the geometry and time scale of the molecular motion. At ambient temperature, the tyrosine ring of sample 5 is rigid and in the sample 6 the phenylalanine ring undergoes a "π -flip". The tyrosine rings of form I of 7 and 8 are static, while the phenylalanine rings of form II of 7 and 8 undergo a fast regime exchange [6]. Variable temperature 2H measurements proved that the tyrosine and phenylalanine rings of two forms of compounds 7 and 8 became more mobile with increasing temperature. In contrast, the aromatic rings of samples 5 and 6 preserve their dynamics regime (static tyrosine and "π -flip" phenylalanine) in a large range of temperatures [6]. The analysis of 13C, 15N labeled tetrapeptide Tyr-D-Ala-Phe-Gly 2’-phospholipid membrane interactions suggests that peptide 2’ is aligned on the surface of the membrane (RFDR MAS) and the sandwich-like π -CH_3-π arrangement of the pharmacophore is preserved (DARR) [7].
Źródło:
Wiadomości Chemiczne; 2012, 66, 9-10; 867-891
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Beef as a source of bioactive components
Mięso wołowe jako źródło składników bioaktywnych
Autorzy:
Sadowska, A.
Waszkiewicz-Robak, B.
Nowosinska, K.
Batogowska, J.
Rakowska, R.
Powiązania:
https://bibliotekanauki.pl/articles/796400.pdf
Data publikacji:
2014
Wydawca:
Szkoła Główna Gospodarstwa Wiejskiego w Warszawie. Wydawnictwo Szkoły Głównej Gospodarstwa Wiejskiego w Warszawie
Tematy:
beef
bioactive component
source
protein
amino acid
peptide
collagen
nutritional value
B-group vitamin
iron
zinc
copper
Opis:
Beef is classified as the most valuable meat in terms of nutritional value. It contains a number of valuable bioactive substances, preferably affecting the functioning of the body. It is a rich source of protein, amino acids, bioactive peptides (including taurine, carnosine, creatine, carnitine) and contains collagen rich with hydroxy acids (hydroxyproline and hudroksylizyne). Beef is also characterized with a high content of B vitamins (especially B₁₂ vitamin), minerals including most of all easily digestible iron, zinc and copper. Moreover, from a nutritional point of view beef fat contains lots of valuable components, such as conjugated linoleic acid (CLA), significant amounts of fatty acids from n-3 group and coenzyme Q₁₀. In comparison with meat obtained from other animals beef derived from animal meat breed is characterized by a low content of intramuscular fat (2–3%) which is connected with low content of saturated fatty acids. At the same time according to the latest data consuming too much red meat can pose a risk to health due to the development of many diseases.
Mięso wołowe pod względem odżywczym zaliczane jest do najwartościowszych mięs. Mięso to jest źródłem wielu cennych substancji bioaktywnych, korzystnie oddziałujących na funkcjonowanie organizmu, bogatym źródłem pełnowartościowego białka, bioaktywnych aminokwasów i peptydów (m.in. tauryny, karnozyny, kreatyny, karnityny) oraz zawiera bogate w hydroksykwasy (hydroksyprolinę i hydroksylizynę) białka kolagenowe. Mięso wołowe charakteryzuje się także wysoką zawartością witamin z grupy B (głównie witaminy B₁₂), składników mineralnych, w tym przede wszystkim łatwo przyswajalnego żelaza, cynku i miedzi. Ponadto tłuszcz wołowy zawiera wiele cennych, z żywieniowego punktu widzenia, komponentów, takich jak: sprzężony kwas linolowy (CLA), znaczne ilości kwasów tłuszczowych z rodziny n-3, czy koenzym Q₁₀. Mięso wołowe pochodzące od zwierząt ras mięsnych cechuje się niską zawartością tłuszczu śródmięśniowego (ok. 2–3%) i z tym związaną niską zawartością kwasów tłuszczowych nasyconych w porównaniu do mięsa pochodzącego od innych gatunków zwierząt. Jednocześnie według najnowszych danych spożywanie zbyt dużych ilości mięsa czerwonego może stwarzać zagrożenie dla zdrowia wskutek rozwoju wielu chorób.
Źródło:
Zeszyty Problemowe Postępów Nauk Rolniczych; 2014, 576
0084-5477
Pojawia się w:
Zeszyty Problemowe Postępów Nauk Rolniczych
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biological characteristics of a new antibacterial peptide and its antibacterial mechanisms against Gram-negative bacteria
Autorzy:
Pei, Z.
Ying, X.
Tang, Y.
Liu, L.
Zhang, H.
Liu, S.
Zhang, D.
Wang, K.
Kong, L.
Gao, Y.
Ma, H.
Powiązania:
https://bibliotekanauki.pl/articles/2087656.pdf
Data publikacji:
2018
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
antimicrobial peptide
biological characteristics
antibacterial mechanism
Gram-negative bacteria
Źródło:
Polish Journal of Veterinary Sciences; 2018, 21, 3; 533-542
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biological evaluation of analogues of an insect neuropeptide proctolin.
Autorzy:
Woźnica, Iwona
Szeszel-Fedorowicz, Wioletta
Rosiński, Grzegorz
Konopińska, Danuta
Powiązania:
https://bibliotekanauki.pl/articles/1043325.pdf
Data publikacji:
2004
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
proctolin analogues
proctolin
insect myotropic peptide proctolin
Opis:
Continuing our studies on proctolin (Arg-Tyr-Leu-Pro-Thr) we performed the synthesis and biological evaluation of 52 analogues substituted in position 2, 3, 4, and 5 of the peptide chain. The peptides were bioassayed for cardiotropic activity in vitro on Tenebrio molitor and myotropic activity on foregut of Schistocerca gregaria. Twenty analogues retained 20-80% of proctolin activity.
Źródło:
Acta Biochimica Polonica; 2004, 51, 1; 115-119
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł

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