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Journal of Advances in Microbiology Research 2021; 2(2): 01-04
E-ISSN: 2709-944X
P-ISSN: 2709-9431
JRM 2021; 2(2): 01-04
© 2021 JRM
www.microbiojournal.com
Received: 01-05-2021
Accepted: 06-06-2021
Emoleila Itoandon
Department of Research and
Development, Almond
Research Foundation,
Chennai, Tamil Nadu, India
Femi Adams
Production Analytical and
Laboratory Management
Department, Federal Institute
of Industrial Research, Nigeria
Tijani Azeez
Production Analytical and
Laboratory Management
Department, Federal Institute
of Industrial Research, Nigeria
Correspondence
Emoleila Itoandon
Department of Research and
Development, Almond
Research Foundation,
Chennai, Tamil Nadu, India
Surface spreading sporulation (SSS) technique for
microfungal purification
Emoleila Itoandon, Femi Adams and Tijani Azeez
DOI: http://dx.doi.org/10.22271/micro.2021.v2.i2a.13
Abstract
A technique was used for the purpose of separating microscopic filamentous molds. The primary aim
was to establish a method that will conveniently distribute vegetative spores across the surface of a
culture medium allowing easy detection of desired strain. A contaminated Sabouraud Dextrose Agar
(SDA) cultured plate previously used for isolation at 25
o
C after 5 days was used for the purpose of this
investigation. The culture plate showed a mixture of probable isolates after incubation period
signifying a case of cross contamination. Following standard laboratory procedure, the following
isolates: Aspergillus Niger, Aspergillus terreus, Penicillium funiculosum and Penicillium chrysogenum
were recovered using the surface spreading technique. The investigation confirmed the level of
microbial co-existence which is often difficult to manage in cases of pollution caused by molds due to
their growth pattern. On the other hand, the practise provided a simple and effective application in
handling purification of multicellular sporulation.
Keywords: nutrients, cross contamination, purification, molds
Introduction
Green computing is the study in which discarding, recycling and building of computers and
Molds are microscopic multicellular filamentous fungi with unique structural and functional
properties. Their growth allow direct contact with the environment and based on different
classification they form various types of effective nutritional habits enabling them cover a
large surface area (Sun et al. 2019)
[15]
. These characteristics make diffusion of nutrient easy
enabling the mold adapt to dehydration. Research activities have shown industrial relevance
which has been justified in the proffering of enzymes, primary and secondary metabolites
(Zhou et al. 2021; Suurbaar et al. 2017, Sunesen and Stahnke, 2003)
[22, 17, 16]
making them
very significant to industrialization.
Their ability to grow in extreme conditions has been related to the protective structured
vegetative spores, which provide high level of modifications for survival (Selbmann et al.
2005)
[14]
. Spores of molds have been recorded to be small in sizes and easily propagated by
wind, rain, insects, animals, and man constituting frequent level of cross contamination
(Maharachchikumbura et al. 2016)
[9]
. Furthermore, with relevance to their sizes and growth
pattern; purification for the purpose of strain identification is often a challenge because: i.
their filaments often easily growing interwoven forming a web across any environmental
surface and ii. Undetected vegetative spores passing through filtration medium causing
progressing contamination. Several techniques have been used for the purpose of micro-
fungi purification and aligned to methods of isolation from samples with common principles
involving: i. single spore isolation method often employed when the fungus produces spores,
which are coloured and bold, and ii. Single hyphal tip method, often used when purifying
fungi which either do not produce spores or produces small and hyaline spores (Fawzi, 2011)
[2]
. Either way, purification still remains a challenge resulting to consistent environmental
pollution. The main objective of this investigation was to develop a simple and cost effective
technique which overcomes the selection between spore or hyphae producers, and also
reduce the time involved in the process of mold identification.
Materials and Methods
Specimen Collection
A contaminated culture plate was retrieved from a research institute located at longitude:
77°10′2.78′′E (77.167441) and latitude: 28°31′43.82′′N (28.52884) in the Northern part of
India.