scholarly journals Natural Products of Marine Macroalgae from South Eastern Australia, with Emphasis on the Port Phillip Bay and Heads Regions of Victoria

Marine Drugs ◽  
2020 ◽  
Vol 18 (3) ◽  
pp. 142 ◽  
Author(s):  
James Lever ◽  
Robert Brkljača ◽  
Gerald Kraft ◽  
Sylvia Urban
Keyword(s):  
Natural Products ◽  
Secondary Metabolites ◽  
Phenolic Acids ◽  
Red Algae ◽  
Brown Algae ◽  
Marine Macroalgae ◽  
Eastern Region ◽  
South Eastern ◽  
Eastern Australia ◽  
Different Types

Marine macroalgae occurring in the south eastern region of Victoria, Australia, consisting of Port Phillip Bay and the heads entering the bay, is the focus of this review. This area is home to approximately 200 different species of macroalgae, representing the three major phyla of the green algae (Chlorophyta), brown algae (Ochrophyta) and the red algae (Rhodophyta), respectively. Over almost 50 years, the species of macroalgae associated and occurring within this area have resulted in the identification of a number of different types of secondary metabolites including terpenoids, sterols/steroids, phenolic acids, phenols, lipids/polyenes, pheromones, xanthophylls and phloroglucinols. Many of these compounds have subsequently displayed a variety of bioactivities. A systematic description of the compound classes and their associated bioactivities from marine macroalgae found within this region is presented.

Three new species of Parmelia subgen. Xanthoparmelia (Lichens) from south-eastern Australia

1976 ◽  
Vol 24 (5) ◽  
pp. 663 ◽  
Author(s):  
JA Elix
Keyword(s):  
New Species ◽  
Secondary Metabolites ◽  
New South ◽  
New South Wales ◽  
Usnic Acid ◽  
Australian Capital Territory ◽  
South Eastern ◽  
South Wales ◽  
Eastern Australia ◽  
Three New Species

Parmelia (subgen. Xanthoparmelia) barbatica, Parmelia (subgen. Xanthoparmelia) burmeisterii and Parmelia (subgen. Xanthoparmelia) pseudohypoleia are described as new from the Australian Capital Territory and New South Wales. The former two species are the first representatives of this subgenus to be described in which usnic acid, barbatic acid and 4-O-demethylbarbatic acid are the major secondary metabolites.

scholarly journals Marine benthic algal flora of Ascension Island, South Atlantic

2014 ◽  
Vol 97 (4) ◽  
pp. 681-688 ◽  
Author(s):  
Konstantinos Tsiamis ◽  
Akira F. Peters ◽  
Dawn M. Shewring ◽  
Aldo O. Asensi ◽  
Pieter Van West ◽  
...  
Keyword(s):  
Atlantic Ocean ◽  
Red Algae ◽  
Brown Algae ◽  
South Atlantic ◽  
Marine Macroalgae ◽  
Algal Flora ◽  
Red Macroalgae ◽  
Ascension Island ◽  
Infraspecific Taxa ◽  
First Time

This paper provides a comprehensive checklist of the marine benthic macroalgal flora of Ascension Island (tropical South Atlantic Ocean), based on both new collections and previous literature. 82 marine macroalgae were identified from our work, including 18 green algae (Ulvophyceae), 15 brown algae (Phaeophyceae) and 49 red algae (Rhodophyta). Among our collections, 38 species and infraspecific taxa are reported for the first time from Ascension Island, including seven green, three brown and 28 red macroalgae, raising the total number of seaweeds recorded in Ascension so far to 112 taxa in species and infraspecific level. No seagrasses have been recorded at Ascension Island.

scholarly journals The Natural Products and Pharmacological Biodiversity of Brown Algae from the Genus Dictyopteris

2021 ◽  
Vol 66 (1) ◽  
Author(s):  
Mohammed I. Rushdi ◽  
Iman A. M. Abdel- Rahman ◽  
Hani Saber ◽  
Eman Zekry Attia ◽  
Usama Ramadan Abdelmohsen
Keyword(s):  
Natural Products ◽  
Secondary Metabolites ◽  
Brown Algae ◽  
Biological Activities ◽  
Biological Properties ◽  
Sulfur Compounds ◽  
Chemical Feature ◽  
Pharmaceutical Applications

Abstract. Genus Dictyopteris is an important genus among marine seaweeds and is excessively distributed and known by its ocean smell due to its secondary metabolites including C11-hydrocarbons and sulfur compounds. This chemical feature is responsible for its interesting biological properties. This review detected the literature from 1959 to 2021 on the genus Dictyopteris and revealed the secondary metabolites, together with biological activities of the genus Dictyopteris to create the base for additional studies on its clinical and pharmaceutical applications.   Resumen. El género Dictyopteris es un género importante entre las algas marinas y está excesivamente distribuido y conocido por su olor a océano debido a sus metabolitos secundarios que incluyen hidrocarburos C11 y compuestos de azufre. Esta característica química es responsable de sus interesantes propiedades biológicas. Esta revisión detectó la literatura de 1959 a 2021 sobre el género Dictyopteris y reveló los metabolitos secundarios, junto con las actividades biológicas del género Dictyopteris, para crear la base para estudios adicionales sobre sus aplicaciones clínicas y farmacéuticas.

scholarly journals Isolation and Structure Elucidation of New Secondary Metabolites from New Zealand Marine Red Algae

2021 ◽  
Author(s):  
◽  
Wendy Lynne Popplewell
Keyword(s):  
Antibacterial Activity ◽  
Natural Products ◽  
New Zealand ◽  
Secondary Metabolites ◽  
Natural Product ◽  
Red Algae ◽  
Structure Elucidation ◽  
Screening Tool ◽  
Product Analysis ◽  
Algal Extracts

<p>The natural product analysis of New Zealand red algae has been neglected in recent years, and there is obvious scope for the chemical re-evaluation of New Zealand marine red algae. This study describes the isolation and structure elucidation of 12 new and eight known compounds from four different genera of red algae. To aid in this process, 34 red algae were screened in order to generate a digital HSQC spectra mask, a screening tool developed by the VUW Marine Natural Products group to identify extracts of interest for further analysis. All 34 algal extracts were screened using the HSQC mask and four extracts were identified as interesting and analysed in detail. Examination of extracts of the red algae Plocamium costatum and Ballia callitricha lead to the isolation of three known metabolites. Eleven new oxylipins, labillarides A to K, are reported from the alga Phacelocarpus labillardieri. Labillarides A to H are polyunsaturated alpha-pyrone macrocycles, all of which show similarities to the previously reported compounds isolated from southern Australian collections of the algae. Labillarides E to H are of particular interest as they represent the two diastereomeric pairs associated with variation at the C-3 and C-8 chiral centres. Labillarides I and J are related enol macrocycles while labillaride K is a furan-3-one oxylipin, all of which have biogenic significance to the macrocyclic alpha-pyrones. Labillarides A, B and I exhibit moderate cytotoxicity while labillaride C shows moderate antibacterial activity. A new nitrogenous bromophenol, colensolide A, was isolated from the alga Osmundaria colensoi along with five known bromophenols. The presence of nitrogen-containing sidechains in bromophenols is unusual but not unprecedented. The bicyclic nitrogenous moiety observed in colensolide A is proposed to be of histidine origin. Several of the known bromophenols exhibit antibacterial activity and one shows moderate cytotoxicity.</p>

scholarly journals Isolation and Structure Elucidation of New Secondary Metabolites from New Zealand Marine Red Algae

2021 ◽  
Author(s):  
◽  
Wendy Lynne Popplewell
Keyword(s):  
Antibacterial Activity ◽  
Natural Products ◽  
New Zealand ◽  
Secondary Metabolites ◽  
Natural Product ◽  
Red Algae ◽  
Structure Elucidation ◽  
Screening Tool ◽  
Product Analysis ◽  
Algal Extracts

<p>The natural product analysis of New Zealand red algae has been neglected in recent years, and there is obvious scope for the chemical re-evaluation of New Zealand marine red algae. This study describes the isolation and structure elucidation of 12 new and eight known compounds from four different genera of red algae. To aid in this process, 34 red algae were screened in order to generate a digital HSQC spectra mask, a screening tool developed by the VUW Marine Natural Products group to identify extracts of interest for further analysis. All 34 algal extracts were screened using the HSQC mask and four extracts were identified as interesting and analysed in detail. Examination of extracts of the red algae Plocamium costatum and Ballia callitricha lead to the isolation of three known metabolites. Eleven new oxylipins, labillarides A to K, are reported from the alga Phacelocarpus labillardieri. Labillarides A to H are polyunsaturated alpha-pyrone macrocycles, all of which show similarities to the previously reported compounds isolated from southern Australian collections of the algae. Labillarides E to H are of particular interest as they represent the two diastereomeric pairs associated with variation at the C-3 and C-8 chiral centres. Labillarides I and J are related enol macrocycles while labillaride K is a furan-3-one oxylipin, all of which have biogenic significance to the macrocyclic alpha-pyrones. Labillarides A, B and I exhibit moderate cytotoxicity while labillaride C shows moderate antibacterial activity. A new nitrogenous bromophenol, colensolide A, was isolated from the alga Osmundaria colensoi along with five known bromophenols. The presence of nitrogen-containing sidechains in bromophenols is unusual but not unprecedented. The bicyclic nitrogenous moiety observed in colensolide A is proposed to be of histidine origin. Several of the known bromophenols exhibit antibacterial activity and one shows moderate cytotoxicity.</p>

A Review of the Components of Seaweeds as Potential Candidates in Cancer Therapy

2018 ◽  
Vol 18 (3) ◽  
pp. 354-366 ◽  
Author(s):  
Ban-Feng Ruan ◽  
Wei-Wei Ge ◽  
Meng-Xue Lin ◽  
Qing-Shan Li
Keyword(s):  
Natural Products ◽  
Cancer Therapy ◽  
Microbial Communities ◽  
Anticancer Agents ◽  
Red Algae ◽  
Brown Algae ◽  
Marine Natural Products ◽  
Antibacterial Properties ◽  
The Novel ◽  
Anticancer Activities

The marine natural products (MNPs) isolated from seaweeds-associated microbial communities have received substantial attention owing to their exceptional nutritional and pharmacology application, such as antiviral, anticancer, antiprotozoal, antifungal, and antibacterial properties and so on. Particularly, there are several MNPs that have been displayed attractive value for the development of novel anticancer agents. This review covers the literature published in the recent 5 years on the novel anticancer MNPs discovered originating from seaweeds, and focused on the chemistry and relative anticancer activities of new MNPs which categorize their source organisms. These seaweed-derived MNPs are categorized based on their origin as brown algae, red algae, cyanobacteria, chlorophyta and others.

Survey of freshwater red algae (Rhodophyta) of south-eastern Australia

1984 ◽  
Vol 35 (2) ◽  
pp. 213 ◽  
Author(s):  
TJ Entwisle ◽  
GT Kraft
Keyword(s):  
Fresh Water ◽  
Red Algae ◽  
Algal Flora ◽  
South Eastern ◽  
Marine Habitats ◽  
Eastern Australia ◽  
Red Algal ◽  
Freshwater Habitats ◽  
Australian Freshwater ◽  
South Eastern Australia

A survey of rivers and other freshwater habitats in south-eastern Australia has resulted in the description and illustration of 14 species and two forms of red algae. With the exception of the two species of Nothocladus, all the taxa appear to be widespread in warm to cool temperate regions of the world. Three of the species [Chroodactylon ornatum (C.Ag.) Basson, Caloglossa leprieurii (Mont.) J.Ag. and Bostrychia scorpioides (Gmel.) Montagne] occur in brackish and marine habitats, as well as in fresh water. Two species [Hildenbrandia rivularis (Liebm.) J.Ag. and Audouinella hermannii Roth] are members of fundamentally marine genera that have one or a few distinct freshwater representatives. The remaining taxa belong to the genus Compsopogon (Compsopogonaceae, Erythropeltidales) and the family Batrachospermaceae (Nemaliales), which have no marine representatives and probably evolved in fresh water. This latter group consists of Compsopogon coeruleus (Balb.) Montagne, Batrachosperrnum atrum (Huds.) Harvey, B. ectocarpum Sirodot, B. Helminthoideum (Sirod.) Mori (two forms), B. keratophytum Bory, B. virgato-decaisneanum Sirodot, Sirodotia suecica Kylin (two forms), Nothocladus nodosus Skuja and N. lindaueri Skuja. The survey has added six new records to the Australian freshwater red algal flora. Nothocladus nodosus Skuja and N. tasmanicus Skuja are synonymized; N. lindaueri Skuja, previously recorded only from New Zealand, was found to be widely distributed in Victoria. Taxonomic characters in the genus Batrachospermum from Australia, the largest and most difficult group of species encountered, are reviewed.

Movements of Cormorants in South Eastern Australia and the Influence of Flood on Breeding

1983 ◽  
Vol 10 (1) ◽  
pp. 149 ◽  
Author(s):  
LC Llewellyn
Keyword(s):  
Great Cormorant ◽  
Eastern Region ◽  
Dispersal Patterns ◽  
South Eastern ◽  
System A ◽  
Large Numbers ◽  
Eastern Australia ◽  
Great Cormorants ◽  
Fish Survival

Examination of flood regimes in inland south-east Australia showed that natural flooding was an important factor in initiating breeding of cormorants, as were small localized artificial floods. Recovery data for banded great, little black and little pied cormorants were examined to assess dispersal patterns from natal colonies. Dispersal of great cormorants was more marked than that of little pied and little black cormorants; many great cormorants from the lower Murray moved upstream. Such dispersal led to the occasional influx of large numbers of birds into the permanent cooler waters of the eastern region of the Murray-Darling system. A case study was examined; it is suggested that the increase in great cormorant numbers can be forecast and should be used to determine the time at which fish are stocked, in order to improve fish survival.

One-step Separation and Purification of Four Phenolic Acids from Stenoloma chusanum (L.) Ching by Medium-pressure Liquid Chromatography and High-speed Counter-current Chromatography

2019 ◽  
Vol 9 (2) ◽  
pp. 138-143
Author(s):  
Tianyun Li ◽  
Xiling Dai ◽  
Yichen Li ◽  
Guozheng Huang ◽  
Jianguo Cao
Keyword(s):  
Natural Products ◽  
Liquid Chromatography ◽  
Phenolic Acids ◽  
High Speed ◽  
High Efficiency ◽  
Total Phenolic ◽  
Medium Pressure ◽  
Medium Pressure Liquid Chromatography ◽  
One Step ◽  
Counter Current

Background:Stenoloma chusanum (L.) Ching is a Chinese traditional medicinal fern with high total flavonoid and total phenolic content. Traditionally, phenolic compounds were separated by using column chromatography, which is relatively inefficient. </P><P> Objective: This study aims to use an efficient method to separate natural products from S. chusanum by Medium-Pressure Liquid Chromatography (MPLC) and High-Speed Counter-Current Chromatography (HSCCC).Methods:In the present research, firstly, a sample (2.5 g) from the dichloromethane extract of S. chusanum was separated by MPLC. Next, fraction P5 was purified by HSCCC with a two-phase solvent system composed of hexane-ethyl acetate-methanol-water (HEMWat) at a volume ratio of 2:4:1:4 (v/v/v/v). </P><P> Result: Four phenolic acids were obtained and their structures were identified by means of NMR and ESI-mass analysis. They were identified as: 1) protocatechuic acid (34 mg, purity 90.1%), 2) syringic acid (66 mg, purity 99.0%), 3) p-hydroxybenzoic acid (5 mg, purity 91.2%) and 4) vanillic acid (6 mg, purity 99.3%).Conclusion:The combination of MPLC and HSCCC is a high-efficiency separation method for natural products. This is the first report with regard to the separation of four phenolic acids in one step by MPLC and HSCCC from S. chusanum (L.) Ching.

scholarly journals Profiles of Secondary Metabolites (Phenolic Acids, Carotenoids, Anthocyanins, and Galantamine) and Primary Metabolites (Carbohydrates, Amino Acids, and Organic Acids) during Flower Development in Lycoris radiata

Biomolecules ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 248
Author(s):  
Chang Ha Park ◽  
Hyeon Ji Yeo ◽  
Ye Jin Kim ◽  
Bao Van Nguyen ◽  
Ye Eun Park ◽  
...  
Keyword(s):  
Amino Acids ◽  
Secondary Metabolites ◽  
Organic Acids ◽  
Phenolic Acids ◽  
Flower Development ◽  
Developmental Stages ◽  
Tca Cycle ◽  
Primary And Secondary Metabolites ◽  
Hydrophilic Compounds ◽  
Tca Cycle Intermediates

This study aimed to elucidate the variations in primary and secondary metabolites during Lycorisradiata flower development using high performance liquid chromatography (HPLC) and gas chromatography time-of-flight mass spectrometry (GC-TOFMS). The result showed that seven carotenoids, seven phenolic acids, three anthocyanins, and galantamine were identified in the L. radiata flowers. Most secondary metabolite levels gradually decreased according to the flower developmental stages. A total of 51 metabolites, including amines, sugars, sugar intermediates, sugar alcohols, amino acids, organic acids, phenolic acids, and tricarboxylic acid (TCA) cycle intermediates, were identified and quantified using GC-TOFMS. Among the hydrophilic compounds, most amino acids increased during flower development; in contrast, TCA cycle intermediates and sugars decreased. In particular, glutamine, asparagine, glutamic acid, and aspartic acid, which represent the main inter- and intracellular nitrogen carriers, were positively correlated with the other amino acids and were negatively correlated with the TCA cycle intermediates. Furthermore, quantitation data of the 51 hydrophilic compounds were subjected to partial least-squares discriminant analyses (PLS-DA) to assess significant differences in the metabolites of L. radiata flowers from stages 1 to 4. Therefore, this study will serve as the foundation for a biochemical approach to understand both primary and secondary metabolism in L. radiata flower development.

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