Physical, Chemical, and Microbial Changes during
Fermentation of Bungkil: A Traditional Snack Originated from
Banyumas, Central Java
Umi Purwandari, Zeilina R. Pangestika, Jamilah, Rakhmawati and M. Fuad Fauzul Muktamar
Department of Agroindustrial Technology, University of Trunojoyo Madura, PO Box 2 Bangkalan, East Java, Indonesia
Keywords: Coconut, Fermentation, Traditional Food.
Abstract: Bungkil is a traditional snack or side dish made from by-product of traditional process of coconut oil making
process, originated from Banyumas and Kebumen regencies, Central Java. We interviewed a bungkil maker
for bungkil making process, in the area of production,. The process includes washing mature coconut kernel,
soaking in water for three days, draining, and first fermentation by wrapping in layers of banana leaf for three
days, draining, grating, second fermentation by wrapping grated coconut in layers of banana leaf for two days,
and sun-drying and oil separation. The by product is the cake, which is called ‘bungkil’. The cake is mixed
with spices, oval or round shaped, and then fried in coconut oil. It is then ready for consumption. We analysed
pH, water activity, and microbial count during fermentation. Results showed that final pH, and water activity
were 7.50, 0.88, respectively. Microbial concentration in fresh coconut was 9.84x10
7
cfu/mL, at the end of
soaking was 4.42x10
9
cfu/mL, and at the end of sun-drying was 2.74x10
9
cfu/mL.
1 INTRODUCTION
There is a rising demand towards traditional food in
international market, which has to be responded by
food industry (Vanhonacker 2013, Kwon 2015).
Recently, consumers highly valued traditional
character in food, and in the same time also required
safety, proper labelling, and availability and easy to
access product in the market (Vanhonacker 2013).
Apart from consumers’ better appreciation to ethnic
foods, traditional food is closely related to utilization
of local produce, local knowledge and technology
(Kwon 2015, Renna 2015), thus support food
security. One of the ancient methods to preserve food
is fermentation where growth of spoilage
microorganisms is inhibited by other beneficial
microorganisms (Kwon 2015). The role of fermented
traditional food in balancing availability of food
sources was also highlighted (Anal 2019). This
process is now well-known as a method having health
supporting effect. There are wide range of traditional
fermented products reported previously (Anal 2019),
however we did not encounter any of them made from
coconut meat fermentation.
However, we found a traditional fermented
coconut meat product in Indonesia. It is called
‘bungkil’ which is originated from Banyumas and
Kebumen, two regencies in southern part of Central
Java. Bungkil may be considered as by-product of
traditional fermentation for coconut oil extraction.
Fermentation is very cheap and easy method for
coconut oil making process (Iskandar 2009), which
can utilize wide range of microorganism including
yeasts (Iskandar 2009), and lactobacilli (Agarwal and
Bosco 2017). Although the process is more suitable
for small enterprise (Iskandar 2009), it is time
consuming and the quality of product was considered
inferior due to poor colour and odor (Agarwal and
Bosco 2017). Bungkil is consumed as a snack or a
side dish to be eaten with rice. Recently, this product
is rarely found in local market. Bungkil makers now
made it based on individual request of consumer.
Unlike a well-known forbidden fermented coconut
product in the area called ‘tempe bongkrek’
(bongkrek tempeh) which can pose fatal poisoning
(Anwar et al. 2017), there is no report on bungkil
poisoning. Therefore, it is important to conduct
preliminary study on fermentation process of bungkil.
In this work, we collected information of bungkil
making process, and subsequently studied some
chemical and microbial profile during fermentation.
Purwandari, U., Pangestika, Z., Jamilah, ., Rakhmawati, . and Muktamar, M.
Physical, Chemical, and Microbial Changes during Fermentation of Bungkil: A Traditional Snack Originated from Banyumas, Central Java.
DOI: 10.5220/0009979400002833
In Proceedings of the 2nd SEAFAST International Seminar (2nd SIS 2019) - Facing Future Challenges: Sustainable Food Safety, Quality and Nutrition, pages 89-92
ISBN: 978-989-758-466-4
Copyright
c
2022 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
89
2 METHODOLOGY
2.1 Stages of Process of Making
Bungkil
We interviewed a ‘bungkil’ maker and previously a’
bungkil’ seller lived in Cilacap, called Ibu Sagem.
After identifying stages of process, we carried out
bungkil fermentation in the laboratory, and decided
stages of process where samples would be collected.
All samples were taken from two separate
experiments, with two data readings in each
parameter in every experiment.
2.2 pH
pH was determined using standard method where
solid sample was grounded using pestle and mortar,
and then diluted using distilled water. Solid was
separated by filtration using Whatman paper no.40.
Determination of pH of filtrate was carried out using
pH-meter (PH 1120X, Mattler Toledo, China).
2.3 Water Activity
Water activity of sample was determined using an
Aw-meter (Hygropalm, Rotronic, Bassersdorf). As
much as 2 gram sample was put inside sample
chamber which was then closed with the lid to start
the reading.
2.4 Microbial Count, Macroscopical,
and Microscopical Observation of
Colonies
A serial dilution was performed for each sample taken
from each stage of process. Then, one milliliter of
suspension was aseptically transferred and spread
evenly onto surface of a plate count agar (Oxoid
CM0325).
3 RESULT AND DISCUSSION
The process of making ‘bungkil’ was described by
Ibu Sagem, and it consisted of several stages. It
started from fresh coconut meat which is washed, and
then soaked in well water or mixed of water with
coconut juice (approximately 1:1, v/v). The soaking
stage took three days at room temperature. After that,
the coconut chunks were drained, and put into a
bamboo basket lined with two or three layers of
banana leaves. The top of the coconut was covered
with two layers of banana leaves. It was left for three
days. This process was called ‘emplep’ or ‘empep’.
After that, coconut chunks were drained and grated.
The grated coconut went into another three-days
‘emplep’ process in a bamboo basket lined with
banana leaves. After that, for four days, grated
coconut was sun-dried during day time, and put into
bamboo basket for ‘emplep’ process during night. At
the end of four days, grated coconut has been very
soft and oily. The oil was separated by hand pressing
of grated coconut wrapped in cheese cloth. The oil
was collected, while the cake was then mixed with
spices (shallot, garlic, chilli, salt, sugar, and
galangal). The mixture was then shaped, and deep
fried in coconut oil previously collected from the
process.
Chemical and microbial changes during stages of
process was presented in Table 1. During ‘emplep’ or
fermentation process, acidity as expressed in pH
reduced from 7 to around 6. It was expected that lactic
acid bacteria may utilize simple sugar of coconut
meat to produce acid during the process. The final
product, however, showed higher pH than that of
fresh coconut. This may due to the formation of basic
substances resulted from protein degradation, such as
ammonia.
Water activity was high during the process, but
reduced to 0.88 after drying. Even after drying, high
water activity was expected, since coconut meat
became very soft and moist during fermentation. The
presence of oil in the product may hinder water
evaporation. High water activity during ’emplep’
facilitated growth of bacteria to increase from 9.84 ×
10
7
cfu/mL to 4.42 ×10
9
during soaking and 2.74 ×
10
9
after drying. We did not identify colonies to
species level, however there was apparently change
in types of microorganism during fermentation.
Colonies isolated from fresh coconut meat was
mostly white and cocci with around 3.3
μm diameter.
During soaking there were orange colonies of
streptobacilli cells, and white colonies of cocci. These
colonies were also isolated from the final product.
As bungkil making process is basically a
fermentation of coconut to produce coconut oil, it
differs from other familiar process where
fermentation was applied to coconut milk (Iskandar
2009) rather than coconut meat. Therefore, chemical
and microbial changes in bungkil fermentation may
not as fast as that in coconut milk fermentation. Final
pH of coconut oil produced by coconut milk
fermentation was 6 (Iskandar, 2009), while the solid
part (locally called as “blondo”) was 4.5 (Iskandar,
2009). The lowest pH in bungkil fermentation was
5.7, slightly lower than that of oil (Iskandar, 2009),
2nd SIS 2019 - SEAFAST International Seminar
90
Table 1: Acidity, water activity, and microbial count of during processing of ‘bungkil’.
Stages of process pH Water
activity
Microbial count
(cell/mL)
Microbial
characteristics
Fresh coconut meat 7.32 0.93
9.84 × 10
7
White, shiny colonies;
cocci, 3.3
μm diameter
Soaking 6.50 0.97
4.42 × 10
9
Orange colonies,
streptobacilli 4-5
μm in
length
White colonies, cocci 4
μm in diameter
White colonies, cocci,
11.3
μm in diameter
Coconut chunks
fermentation
6.63 0.97 Not analysed
Grated coconut fermentation 5.76 0.95 Not analysed
Coconut cake after drying 7.50 0.88
2.74 × 10
9
White colonies, cocci,
2.1
μm
Orange colonies,
streptococci, 4.5
μm in
length
but more basic than solid part of coconut milk
(Iskandar 2009). There was an increase of pH during
final of bungkil process after drying, to reach 7.5.
Therefore, bungkil process may be categorized as
alkaline fermentation (Anal 2019), where bacilli may
be predominated (Anal 2019). Lypolitic and
proteolytic activities during bungkil fermentation was
likely to produce basic substances such as ammonia.
Micrococci, which is characterized by small
diameter cell (0.5-3
μm), were isolated in several
coconut-based product, such as dried grated coconut
(Kinderlerer and Clark 1986), coconut milk (Suryani
et al. 2014), fresh coconut (Su’i et al. 2015), coconut
water (Salunkhe and Kadam 1995), and copra
(Salunkhe and Kadam 1995). Coconut meat was a
rich medium for growth of contaminating
microorganism (Umesha and Nrayanaswamy 2016),
as compared to coconut water (Umesha and
Narayanaswamy 2016). Although micrococci maybe
considered as spoilage bacteria which can be
inhibited by lactic acid bacteria (Gollop et al. 2006),
they showed growth stimulation effect to lactic acid
bacteria (Nath and Wagner 1973b) by inhibition of
hydrogen peroxide production (Nath and Wagner
1973a).
During bungkil fermentation, lactic acid bacteria
growth is expected, as indicated by reduced pH.
Lactic acid bacteria was reported to grow during
coconut milk spontaneous fermentation (Suryani et
al. 2014, Agarwal and Bosco 2017). Suitability of
coconut meat for lactic acid bacteria growth is also
shown by production coconut milk kefir employing
Lactobacillus spp. (Lakshmi and Pramela 2018).
Lactic acid bacteria are abundant in tropical
environment, including some species of lactobacilli,
Leuconostoc sp., Weisella sp. and Lactococcus lactis
(Khota et al. 2016).
4 CONCLUSION
Bungkil making process involved acidic fermentation
in early stage and basic fermentation in the later stage,
by cocci and streptobaccilli.
Physical, Chemical, and Microbial Changes during Fermentation of Bungkil: A Traditional Snack Originated from Banyumas, Central Java
91
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