scholarly journals Isolasi Dan Identifikasi Senyawa Metabolit Sekunder Ekstrak n-Heksana Tumbuhan Cakar Ayam (Selaginella plana Hieron)

2019 ◽  
Vol 19 (2) ◽  
pp. 178
Author(s):  
Mitamoriska Mitamoriska ◽  
Sumiati Side ◽  
Pince Salempa
Keyword(s):  
Melting Point ◽  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Ir Spectrum ◽  
Hexane Extract ◽  
White Crystal ◽  
Steroid Compound

ABSTRAK Penelitian ini bertujuan untuk mengisolasi dan mengidentifikasi senyawa metabolit sekunder yang terdapat dalam ekstrak n-heksana tumbuhan cakar ayam (Selaginella plana Hieron). Penelitian dilakukan melalui beberapa tahap yaitu preparasi sampel, maserasi dengan metanol, partisi dengan n-heksana, fraksinasi, pemurnian, dan identifikasi. Isolat diperoleh dalam bentuk kristal jarum berwarna putih dengan titik leleh 128 – 1300C dan memberikan hasil positif pada pereaksi Lieberman-Buchard. Dan spektrum IR isolat menunjukkan adanya gugus -OH (3425,58 cm-1), CH3- dan -CH2- alifatik (2958,80 cm-1; 2929,87 cm-1; 2895,15 cm-1; dan 2866,22 cm-1), C=C alkena (1641,42 cm-1), CH3- dan -CH2- tekuk (1462,04 cm-1 dan 1377,17 cm-1), C-O (1058,92 cm-1), =C-H (962,48 cm-1). Berdasarkan data tersebut disimpulkan bahwa isolat yang diperoleh merupakan golongan steroid. Kata kunci : Isolasi, Selaginella plana Hieron, Metabolit Sekunder, Steroid ABSTRACT The purpose of this research was to isolate and identifed the secondary metabolite compound from n-hexane extract of Cakar Ayam (Selaginella plana Hieron) plants. This research was carried out in several steps, they were preparation of sample, maceration with methanol, partition with n-hexane, fractination, purification, and identification. The isolate obtaned was white crystal needle shaped with melting point to 128-1300C and gave positive respon to the Liebermann-Buchard test. The IR spectrum of the isolate showed the presence of -OH (3425,58 cm-1),CH3- and -CH2- alifatic (2958,80 cm-1; 2929,87 cm-1; 2895,15 cm-1; and 2866,22 cm-1),C=C alkena (1641,42 cm-1),CH3- and -CH2- bending (1462,04 cm-1 and 1377,17 cm-1), C-O (1058,92 cm-1),=C-H (962,48 cm-1). Based on those result, it was concluded that the isolate was a steroid compound. Keywords : Isolation, Selaginella plana Hieron, Secondary Metabolites, Steroid

scholarly journals Isolasi dan Identifikasi Senyawa Metabolit Sekunder Ekstrak n-Heksana Batang Benalu (Dendrophthoe falcata (L.f) Ettingsh)

2019 ◽  
Vol 20 (2) ◽  
pp. 142
Author(s):  
Herianti Hasbullah ◽  
Sudding Sudding ◽  
Netti Herawati
Keyword(s):  
Melting Point ◽  
Secondary Metabolite ◽  
Ir Spectrum ◽  
Hexane Extract ◽  
Exploratory Research ◽  
Crystal Shape ◽  
Needle Crystal ◽  
Wave Numbers ◽  
Test Result ◽  
Dendrophthoe Falcata

ABSTRAK Penelitian ini adalah penelitian eksplorasi yang bertujuan untuk mengisolasi senyawa metabolit sekunder yang terdapat dalam ekstrak n- heksana batang benalu pohon kakao Dendrophthoe falcata (L.f) Ettingsh, yang berasal dari Desa Cendana, Kec. Burau, Kab. Luwu Timur Makassar, Sulawesi Selatan. Isolasi dilakukan dalam beberapa tahap yaitu maserasi, partisi dengan n-heksana, fraksinasi, uji kemurnian dan identifikasi. Hasil penelitian berupa isolat murni berbentuk kristal jarum berwarna putih dengan titik leleh 1400C. Hasil uji dengan pereaksi wagner membentuk endapan cokelat. Identifikasi dengan spektrum infra merah yang menunjukkan bilangan gelombang (cm-1) yakni: 3550,95 (N-H); 1696,36 (C=O); 1303,88 (CN), 2945,30 dan 2856,58 (CH alifatik), 883,40 (C-H aromatik), 1454,33 (C=C). Berdasarkan hasil IR dan Uji warna menunjukkan bahwa isolat diduga senyawa golongan alkaloid. Kata kunci : Isolasi Dendrophthoe falcata (L.f) Ettingsh, senyawa alkaloid ABSTRACT This study is exploratory research that aimed to isolate and identify the secondary metabolite compound contained in the n-hexane extract of D.falcata (L.f) Ettingsh from Cendana village, Burau district, Luwu Timur Regency of Makassar. Isolation is done in several stages; maceration, partitioning with n-hexane, fractionation, purification and dentification. The result was in pure needle crystal shape with a melting point of 140,2°C. The test result with the Wagner reagent test showed the formation of a brown precipited. Analyzing of IR Spectrum of Isolate showed Several wave numbers; 3550,95 (N-H); 1696,36 (C=O); 1303,88 (CN), 2945,30 dan 2856,58 (CH alifatik), 883,40 (C-H aromatik), 1454,33 (C=C). Based on the result of IR datas and reagen test it is suggest that the isolate is alkaloid compound. Keywords : Isolation, Dendrophthoe falcata (L.f) Ettingsh, alkaloid compound

scholarly journals Antibacterial Activity of Secondary Metabolite Compounds in Ethylacetate Extract of Rumput Mutiara (Hedyotis corymbosa (L.) Lamk)

2019 ◽  
Vol 967 ◽  
pp. 38-44
Author(s):  
Pince Salempa ◽  
Muharram ◽  
Rika Fajri
Keyword(s):  
Antibacterial Activity ◽  
Melting Point ◽  
Absorption Band ◽  
Traditional Medicine ◽  
Secondary Metabolite ◽  
Ir Spectrum ◽  
Diffusion Method ◽  
White Crystal ◽  
The Family ◽  
Wave Numbers

Plant Rumput Mutiara (Hedyotiscorymbosa (L.) Lamk) is one of the family species of Rubiaceae which is used as a traditional medicine that is effective in healing boils, acne, anti-inflammatory, and anticancer. Research methods include maceration, fractionation, purification, class test and bioactivity test with Kirby-Bauer diffusion method using E.coli bacteria. The results of this research are pure isolates with white crystal needle shape with melting point 137-138°C. Pure isolates were analyzed using FTIR, and by the IR spectrum which showed the absorption band at wave numbers 3435.22 cm-1 indicated the presence of –OH, CH3 and-CH2- aliphatic groups (2956.87 cm-1; 2935.66 cm-1; 2893.22 cm-1; and 2866.22 cm-1), C = C (1641.42 cm-1), -CH3 and-CH2- bending (1462.04 cm-1 and 1377.17 cm- 1), CO (1056.99 cm-1), and = CH (964.41 cm-1). Based on the result, it showed that the isolate was steroid group which has low antibacterial activity againts E.coli with inhibition power of 10 mm.

Genome sequence of Novosphingobium malaysiense strain MUSC 273T, novel alpha-proteobacterium isolated from intertidal soil

2018 ◽  
Vol 1 (1) ◽  
Author(s):  
Hooi-Leng Ser ◽  
Wai-Fong Yin ◽  
Kok-Gan Chan ◽  
Nurul-Syakima Ab Mutalib ◽  
Learn-Han Lee
Keyword(s):  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Genome Sequence ◽  
Catalase Activity ◽  
Gene Clusters ◽  
Rrna Genes ◽  
Gram Negative ◽  
Genomic Features

Novosphingobium malaysiense strain MUSC 273T is a recently identified Gram-negative, aerobic alpha-proteobacterium. The strain was isolated from intertidal soil with strong catalase activity. The genome sequence comprises 5,027,021 bp, with 50 tRNA and 3 rRNA genes. Further analysis identified presence of secondary metabolite gene clusters within genome of MUSC 273T. Knowledge of the genomic features of the strain may allow further biotechnological exploitation, particularly for production of secondary metabolites as well as production of industrially important enzymes

Regio- and stereoselective intermolecular phenol coupling enzymes in secondary metabolite biosynthesis

2021 ◽  
Author(s):  
Wolfgang Hüttel ◽  
Michael Müller
Keyword(s):  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Metabolic Pathways ◽  
Cyp Enzymes ◽  
Secondary Metabolite Biosynthesis

Phenol coupling enzymes, especially laccases and CYP-enzymes create an enormous diversity of biarylic secondary metabolites in fungi, plants, and bacteria. The enzymes and the elucidation of the corresponding metabolic pathways are presented.

scholarly journals Vibrio gazogenes inhibits aflatoxin production through downregulation of aflatoxin biosynthetic genes in Aspergillus flavus

2022 ◽  
Author(s):  
Shyam L. Kandel ◽  
Rubaiya Jesmin ◽  
Brian M. Mack ◽  
Rajtilak Majumdar ◽  
Matthew K. Gilbert ◽  
...  
Keyword(s):  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Aspergillus Flavus ◽  
Fungal Biomass ◽  
Expression Profiles ◽  
Health Hazard ◽  
Gene Clusters ◽  
Aflatoxin Contamination ◽  
Aflatoxin Biosynthesis ◽  
Control Samples

Aspergillus flavus is an opportunistic pathogen of oilseed crops such as maize, peanut, cottonseed, and tree nuts and produces carcinogenic secondary metabolites known as aflatoxins during seed colonization. Aflatoxin contamination not only reduces the value of the produce but also is a health hazard to humans and animals. Previously, we observed inhibition of A. flavus aflatoxin biosynthesis upon exposure to the marine bacterium, Vibrio gazogenes (Vg). In this study, we used RNA sequencing to examine the transcriptional profiles of A. flavus treated with both live and heat-inactivated dead Vg and control samples. Fungal biomass, total accumulated aflatoxins, and expression profiles of genes constituting secondary metabolite biosynthetic gene clusters were determined at 24, 30, and 40 h after treatment. Statistically significant reductions in total aflatoxins were detected in Vg-treated samples as compared to control samples at 40 h. But no statistical difference in fungal biomass was observed upon these treatments. The Vg treatments were most effective on aflatoxin biosynthesis as was reflected in significant downregulation of majority of the genes in the aflatoxin gene cluster including the aflatoxin pathway regulator gene, aflR. Along with aflatoxin genes, we also observed significant downregulation in some other secondary metabolite gene clusters including cyclopiazonic acid and aflavarin, suggesting that the treatment may inhibit other secondary metabolites as well. Finally, a weighted gene correlation network analysis identified an upregulation of ten genes that were most strongly associated with Vg-dependent aflatoxin inhibition and provide a novel start-point in understanding the mechanisms that result in this phenomenon.

scholarly journals Urgensi dan Mekanisme Biosintesis Metabolit Sekunder Mikroba Laut

2012 ◽  
Vol 10 (2) ◽  
pp. 120 ◽  
Author(s):  
Risa Nofiani
Keyword(s):  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Metabolic Pathways ◽  
Abiotic Factors ◽  
Biologically Active ◽  
Secondary Metabolite Production ◽  
Marine Microorganism ◽  
Metabolite Production ◽  
Biotic And Abiotic Factors ◽  
Living Materials

Marine microorganism is one of biologically active potential resources of secondary metabolites. Its potency areso promising that the knowledge of how its secondary metabolite occured need to be studied and collected. Thoseknowledges will enable further study is improving secondary metabolite production in the laboratory. In nature,secondary metabolites synthesis occur when there are effect of both biotic and abiotic factors such as sea waterand microbe symbiosis with other living materials. When this is explained in metabolic pathways, secondarymetabolite synthesis affected by available nutrient and regulated by autoinducer molecules through quorum sensingmechanism

scholarly journals Phylogenetic Distribution of Secondary Metabolites in the Bacillus subtilis Species Complex

mSystems ◽  
2021 ◽  
Vol 6 (2) ◽  
Author(s):  
Kat Steinke ◽  
Omkar S. Mohite ◽  
Tilmann Weber ◽  
Ákos T. Kovács
Keyword(s):  
Bacillus Subtilis ◽  
Secondary Metabolites ◽  
Secondary Metabolite ◽  
Species Complex ◽  
Gene Clusters ◽  
Biosynthetic Gene ◽  
Biosynthetic Gene Clusters ◽  
Content Type ◽  
Frameshift Mutations ◽  
Metabolite Production

ABSTRACT Microbes produce a plethora of secondary (or specialized) metabolites that, although not essential for primary metabolism, benefit them to survive in the environment, communicate, and influence cell differentiation. Biosynthetic gene clusters (BGCs), responsible for the production of these secondary metabolites, are readily identifiable on bacterial genome sequences. Understanding the phylogeny and distribution of BGCs helps us to predict the natural product synthesis ability of new isolates. Here, we examined 310 genomes from the Bacillus subtilis group, determined the inter- and intraspecies patterns of absence/presence for all BGCs, and assigned them to defined gene cluster families (GCFs). This allowed us to establish patterns in the distribution of both known and unknown products. Further, we analyzed variations in the BGC structures of particular families encoding natural products, such as plipastatin, fengycin, iturin, mycosubtilin, and bacillomycin. Our detailed analysis revealed multiple GCFs that are species or clade specific and a few others that are scattered within or between species, which will guide exploration of the chemodiversity within the B. subtilis group. Surprisingly, we discovered that partial deletion of BGCs and frameshift mutations in selected biosynthetic genes are conserved within phylogenetically related isolates, although isolated from around the globe. Our results highlight the importance of detailed genomic analysis of BGCs and the remarkable phylogenetically conserved erosion of secondary metabolite biosynthetic potential in the B. subtilis group. IMPORTANCE Members of the B. subtilis species complex are commonly recognized producers of secondary metabolites, among those, the production of antifungals, which makes them promising biocontrol strains. While there are studies examining the distribution of well-known secondary metabolites in Bacilli, intraspecies clade-specific distribution has not been systematically reported for the B. subtilis group. Here, we report the complete biosynthetic potential within the B. subtilis group to explore the distribution of the biosynthetic gene clusters and to reveal an exhaustive phylogenetic conservation of secondary metabolite production within Bacillus that supports the chemodiversity within this species complex. We identify that certain gene clusters acquired deletions of genes and particular frameshift mutations, rendering them inactive for secondary metabolite biosynthesis, a conserved genetic trait within phylogenetically conserved clades of certain species. The overview guides the assignment of the secondary metabolite production potential of newly isolated Bacillus strains based on genome sequence and phylogenetic relatedness.

scholarly journals Antibacterial activity of Escherichia coli from squid ink (Loligo sp.) n-Hexane extracts

2021 ◽  
Vol 869 (1) ◽  
pp. 012033
Author(s):  
D R Utami ◽  
I Irwan ◽  
S Agustina ◽  
S Karina ◽  
S Afriani
Keyword(s):  
Escherichia Coli ◽  
Antibacterial Activity ◽  
Secondary Metabolite ◽  
Bioactive Compound ◽  
Inhibition Zone ◽  
Hexane Extract ◽  
Inhibition Zone Diameter ◽  
E Coli ◽  
Hexane Extracts ◽  
Intermediate Concentration

Abstract Squid is one of the export commodities in Indonesia. In general, the use of squid meat, while the ink is only as waste. In fact, Squid ink contain bioactive compound that potential as anti-inflammatory, antihypertensive, anti-diabetic,anti-microbial and anti-malaria agents. The purpose of the study is to determine the types of secondary metabolite compounds contained in n-hexane extract of Loligo sp. ink using maceration method to determine its antibacterial activity against Escherichia coli. The results of secondary metabolite compounds obtained from the n-hexane extract of Loligo sp. ink are alkaloid, saponins, glycosides and phenol. The results of antibacterial test against E. coli using the disc method obtained the average of inhibition zone diameter at the concentration of 4% is 6.3 mm (intermediate), concentration of 8% is 7.83 mm (intermediate), concentration of 16% is 14.5 mm (susceptible) and concentration of 32% is 10.83 mm (intermediate). The antibacterial activity in n-hexane extract of Loligo sp. ink is optimal at the concentration of 16% against E. coli bacteria.

scholarly journals Isolation of sea cucumbers’s (Holothuria atra) secondary metabolite using column-chromatography technique

2021 ◽  
Vol 869 (1) ◽  
pp. 012010
Author(s):  
S Agustina ◽  
S Bella ◽  
S Karina ◽  
I Irwan ◽  
M Ulfah
Keyword(s):  
Secondary Metabolites ◽  
Ethyl Acetate ◽  
Secondary Metabolite ◽  
Column Chromatography ◽  
Extraction Method ◽  
Sea Cucumber ◽  
Sea Cucumbers ◽  
Marine Chemistry ◽  
Holothuria Atra ◽  
Metabolite Content

Abstract Identification of sea cucumbers from Benteng Inong Balee, Aceh Besar and their phytochemistry screening were conducted in December 2020 to January 2021 at Laboratory of Marine Chemistry and Fisheries Biotechnology, Universitas Syiah Kuala. The purpose of this study was to identify the species of sea cucumbers and its secondary metabolite content using phytochemistry screening and column chromatography. The species of sea cucumbers that were identified was Holothuria atra. The extraction method used in sea cucumber extraction was maceration method, while the separation of secondary metabolites used column-chromatography with eluent of n-hexane : ethyl acetate (8:4). The results showed that secondary metabolites obtained from phytochemical tests were flavonoids, saponins and triterpenoids.

Sign in / Sign up

Export Citation Format

Share Document