Malaysian
Journal of Analytical Sciences Vol 26 No 1
(2022): 96 - 108
ELICITATION
OF INDUCED POLYKETIDE COMPOUNDS FROM A CO-CULTURE BETWEEN Streptomyces sp. STRAIN SUK10 AND Fusarium sp. AND THEIR ANTIBACTERIAL ACTIVITIES
(Elisitasi Sebatian Poliketida Teraruh
daripada Satu Kultur-bersama di antara Streptomyces
sp. Strain SUK10 dan Fusarium sp. dan
Aktiviti Antibakteria)
Muhammad Asyraf Zawawi1,
Nurul Izzati Rosdi1, Noor Wini Mazlan1,2*, Mariam Taib1,
Kamariah Bakar2, Noraziah Mohamad Zin3, Siti
Nordahliawate M. Sidique4, Saif Aldeen Mohammad Fayiz Jaber5, RuAngelie Edrada-Ebel5
1Faculty of
Science and Marine Environment
2Institute of
Marine Biotechnology
Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu,
Malaysia
3Center
for Diagnostic, Therapeutic and Investigative Studies, Faculty of Health
Sciences,
Universiti
Kebangsaan Malaysia, Jalan Raja Muda Abd Aziz, 50300 Kuala Lumpur, Malaysia
4Faculty
of Fisheries and Food Science,
Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu,
Malaysia
5Strathclyde
Institute of Pharmacy and Biomedical Sciences,
University
of Strathclyde, The John Arbuthnott Building, 161 Cathedral Street, Glasgow G4
0RE, Scotland
*Corresponding
author: noorwini@umt.edu.my
Received: 3 November
2021; Accepted: 30 December 2021; Published:
25 February 2022
Abstract
Endophytes
including bacteria and fungi produce
an array of biologically active secondary
metabolites. Different approaches have
been applied in order to increase the probability production of new metabolites
including mimicking the environment, media and the microbes. However, the use
of single culture usually re-produces known compounds with known bioactivities.
Therefore, co-culturing between Streptomyces sp. strain SUK10 and Fusarium
sp. in the same media at different growth stages leads to direct
interaction which may trigger the expression of "silent" biosynthetic pathway
to produce novel secondary metabolites. In this study, we elicited the
production of the unknown secondary metabolites from co-culture extracts by
using high resolution liquid chromatography-mass
spectrometry, while data was processed by utilizing the quantitative
expression analysis software MZmine 2.40.1 and SIMCA P+ 15.0 coupled with macro
analysis and supported with DNP database for dereplication studies. The results
showed that only the extract from co-culture of F7S15 showed enhances antibacterial
activity on the Gram-positive bacteria with minimum inhibition concentration
(MIC) values of 5 mg/mL and 10 mg/mL against Micrococcus sp. and Staphylococcus
aureus, respectively, compared with their independent and other co-culture
extracts were non-active. However, all extracts were non-active on the
Gram-negative bacteria. Our preliminary results showed that the potential of
co-culture method leading the production of novel metabolites which could be
explored for future antibacterial agents.
Keywords: co-culture, metabolomics,
liquid chromatography-mass spectrometry, multivariate analysis, dereplication
Abstrak
Endofit
termasuk bakteria dan fungus menghasilkan satu tatasusunan metabolit sekunder
yang mempunyai keaktifan biologi. Pelbagai pendekatan telah digunakan bagi
tujuan meningkatkan kebarangkalian penghasilan metabolit baru termasuk mengajuk
persekitaran, media dan mikrob. Walaubagaimanapun, penggunaan kultur tunggal
selalumya menghasilkan semula sebatian dengan bioaktiviti yang telah diketahui.
Oleh itu, satu pengkulturan bersama di antara Streptomyces sp. strain
SUK10 dan Fusarium sp. di dalam media yang sama di peringkat pertumbuhan
yang berbeza, memacu kepada interaksi yang mungkin pencetus kepada ungkapan
laluan biosintetik senyap untuk menghasilkan metabolit sekunder baru. Dalam
kajian ini, kami telah memperolehi penghasilan metabolit sekunder yang belum
diketahui daripada ekstrak kultur bersama dengan menggunakan kromatografi
cecair-spektrometri jisim resolusi tinggi, sementara itu data telah dianalisis
menggunakan perisian analisis ungkapan kuantitatif MZmine 2.40.1 dan SIMCA P+
15.0 beserta analisis makro dan disokong oleh pengkalan data DNP bagi kajian
dereplikasi. Keputusan telah menunjukkan bahawa hanya ekstrak daripada kultur
bersama F7S15 telah menunjukkan peningkatan aktiviti antibakteria ke atas
bakteria Gram-positif dengan nilai minimum kepekatan perencatan (MIC) 5 mg/mL
dan 10 mg/mL melawan Micrococcus sp.
dan Staphylococcus aureus,
masing-masing, berbanding ekstrak kutur bebas dan kultur bersama yang lain
adalah tidak aktif. Walaubagaimanapun, semua ekstrak tidak aktif ke atas
bakteria Gram-negatif. Keputusan awal kajian kami telah menunjukkan potensi
kaedah kultur bersama memacu penghasilan metabolit baru yang boleh diterokai
bagi agen antibakteria masa hadapan.
Kata
kunci: kultur
bersama, metabolomik, kromatografi cecair-spektrometri jisim, analisis
multivariat, dereplikasi
Graphical Abstract
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