Protoplast isolation from Dictyopteris pacifica and Scytosiphon lomentaria, using a simple commercial enzyme preparation
Background Protoplasts (i.e., naked plant cells) can be used for in vitro manipulations and genetic improvement in cultivars with economic value. During the last decade, protoplast research in economic brown algae has been scarce, and it is usually hampered by the use of non-commercial enzymes or cr...
Gespeichert in:
Veröffentlicht in: | Journal of Genetic Engineering and Biotechnology 2021-09, Vol.19 (1), p.135-7, Article 135 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background
Protoplasts (i.e., naked plant cells) can be used for in vitro manipulations and genetic improvement in cultivars with economic value. During the last decade, protoplast research in economic brown algae has been scarce, and it is usually hampered by the use of non-commercial enzymes or crude extracts for isolating protoplasts.
Dictyopteris pacifica
is part of a brown algal genus well known by its wide chemical diversity and biological properties.
Scytosiphon lomentaria
is an edible brown seaweed with antioxidant, antitumor, and antiviral properties. So far, there are no protoplast isolation protocols using commercial enzymes for these two economic brown algae. In this study, we obtained protoplasts from cultured samples of
D
.
pacifica
and
S
.
lomentaria
using commercially available enzymes. Additionally, we investigated the effects of Driselase inclusion and Ca-chelation pre-treatment on protoplast yields in order to optimize the conditions for protoplast preparations.
Results
Protoplasts were isolated from
Dictyopteris pacifica
and
Scytosiphon lomentaria
using the commercially available Cellulase Onozuka RS (1%) and Alginate lyase (4 U mL
−1
), and short incubation time (4 h). Driselase did not show significant effects on protoplast production in both species. Ca-chelation pre-treatment only increased the number of protoplasts in
D
.
pacifica
. Under optimal conditions, the protoplast yields from
D
.
pacifica
and
S
.
lomentaria
were 4.83 ± 2.08 and 74.64 ± 32.49 × 10
6
protoplasts g
−1
fresh weight, respectively. The values obtained for
S
.
lomentaria
were 2–3 orders of magnitude higher than previously reported.
Conclusions
Our results show that high protoplast yields can be obtained from
D
.
pacifica
and
S
.
lomentaria
using a simple mixture of commercial enzymes (Cellulase RS and Alginate lyase) and short incubation time (4 h). This work also represents the first report of protoplast isolation in
D
.
pacifica
. The method proposed here can help to expand protoplast technology in more brown algal species. |
---|---|
ISSN: | 1687-157X 2090-5920 |
DOI: | 10.1186/s43141-021-00226-y |