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1.
J Agric Food Chem ; 71(23): 9175-9186, 2023 Jun 14.
Artigo em Inglês | MEDLINE | ID: mdl-37252901

RESUMO

The underlying mechanisms of Cinnamomum kanehirae-stimulated growth and metabolism of Antrodia camphorata remain unknown. Herein, we first observed that the methanol extract of C. kanehirae trunk (MECK) (2 g/L) showed a potent stimulatory effect on A. camphorata triterpenoids production (115.6 mg/L). Second, MECK treatment considerably increased the category and abundance of many secondary metabolites in the mycelia. We identified 93 terpenoids (8 newly formed and 49 upregulated) in the MECK-treated mycelia, wherein 21 terpenoids were the same as those in the fruiting bodies. Third, 42 out of the 93 terpenoids were annotated in the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, mainly involving monoterpenoids and diterpenoids syntheses. Finally, 27 monoterpenes and 16 sesquiterpenes were detected in the MECK, and the two terpenoids with the highest abundance (linalool and α-pinene) were selected for verification and found to considerably increase the terpenoids production of A. camphorata and demonstrate the regulation of mRNA expression levels of nine key genes in the mevalonate pathway via RT-qPCR. This study is beneficial for elucidating the terpenoids synthesis mechanism in A. camphorata.


Assuntos
Antrodia , Cinnamomum , Triterpenos , Fermentação , Terpenos/farmacologia , Terpenos/metabolismo , Triterpenos/farmacologia , Triterpenos/metabolismo , Monoterpenos/farmacologia , Monoterpenos/metabolismo , Metabolômica , Extratos Vegetais/farmacologia , Extratos Vegetais/metabolismo , Antrodia/metabolismo
2.
Crit Rev Biotechnol ; 41(8): 1257-1278, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33985392

RESUMO

Owing to their numerous nutritional and bioactive functions, phospholipids (PLs), which are major components of biological membranes in all living organisms, have been widely applied as nutraceuticals, food supplements, and cosmetic ingredients. To date, PLs are extracted solely from soybean or egg yolk, despite the diverse market demands and high cost, owing to a tedious and inefficient manufacturing process. A microbial-based manufacturing process, specifically phospholipase D (PLD)-based biocatalysis and biotransformation process for PLs, has the potential to address several challenges associated with the soybean- or egg yolk-based supply chain. However, poor enzyme properties and inefficient microbial expression systems for PLD limit their wide industrial dissemination. Therefore, sourcing new enzyme variants with improved properties and developing advanced PLD expression systems are important. In the present review, we systematically summarize recent achievements and trends in the discovery, their structural properties, catalytic mechanisms, expression strategies for enhancing PLD production, and its multiple applications in the context of PLs. This review is expected to assist researchers to understand current advances in this field and provide insights for further molecular engineering efforts toward PLD-mediated bioprocessing.


Assuntos
Fosfolipase D , Biocatálise , Catálise , Fosfolipase D/genética , Fosfolipase D/metabolismo , Fosfolipídeos , Glycine max
3.
Bioengineered ; 9(1): 80-89, 2018 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-28509615

RESUMO

Phosphatidylserine (PS) is useful as the additive in industries for memory improvement, mood enhancement and drug delivery. Conventionally, PS was extracted from soybeans, vegetable oils, egg yolk, and biomass; however, their low availability and high extraction cost were limiting factors. Phospholipase D (PLD) is a promising tool for enzymatic synthesis of PS due to its transphosphatidylation activity. In this contribution, a new and uncharacterized PLD was first obtained from GenBank database via genome mining strategy. The open reading frame consisted of 1614 bp and potentially encoded a protein of 538-amino-acid with a theoretical molecular mass of 60 kDa. The gene was successfully cloned and expressed in Escherichia coli. Its enzymatic properties were experimentally characterized. The temperature and pH optima of PLD were determined to be 60°C and 7.5, respectively. Its hydrolytic activity was improved by addition of Ca2+ at 5 mM as compared with the control. The enzyme displayed suitable transphosphatidylation activity and PS could be synthesized with L-serine and soybean lecithin as substrates under the catalysis of PLD. This PLD enzyme might be a potential candidate for industrial applications in PS production. To the best of our knowledge, this is the first report on genome mining of PLDs from GenBank database.


Assuntos
Proteínas de Bactérias/metabolismo , Genoma Bacteriano , Fosfatidilserinas/biossíntese , Fosfolipase D/metabolismo , Streptomyces/química , Proteínas de Bactérias/genética , Clonagem Molecular , Mineração de Dados , Bases de Dados Genéticas , Escherichia coli/genética , Escherichia coli/metabolismo , Expressão Gênica , Vetores Genéticos/química , Vetores Genéticos/metabolismo , Cinética , Lecitinas/metabolismo , Peso Molecular , Fases de Leitura Aberta , Fosfolipase D/genética , Filogenia , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Serina/metabolismo , Streptomyces/classificação , Streptomyces/enzimologia , Especificidade por Substrato , Temperatura
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