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ANALISIS PROSES PEMBUATAN TEMPE MELALUI CARA PRODUKSI HIGIENIS DAN PENDEKATAN MOLEKULER

Life Science · Vol. 5 No. 1 (2017) · pp. 9–17

ISSN
2528-5009, 2252-6277
Published
2017-02-28
Publisher
Universitas Negeri Semarang
Language
eng

Abstract

Hampir semua tahapan pembuatan tempe merupakan tahap kritikal, sehingga dalam pembuatannya perlu menerapkan prinsip hieginis. Penelitian ini bertujuan untuk mengidentifikasi ada tidaknya kontaminasi bakteri Escherichia coli pada tempe segar dan untuk memprediksi kemungkinan faktor penyebab kontaminasi tersebut di sentra industri tempe Semarang Barat. Observasi dilakukan pada 17 industri tempe di Semarang Barat. Pengujian molekuler secara berturut-turut dilakukan dengan isolasi DNA, analisis DNA menggunakan primer 16E1/E2, dan uji mikrobiologi menggunakan medium Endo Agar. Berdasarkan hasil observasi, 16 industri tempe teridentifikasi ada bakteri E.coli. Satu industri tempe tidak teridentifikasi ada bakteri E.coli. Hal ini ada hubungannya terhadap diterapkannya cara produksi higienis. Hasil yang diperoleh dari isolasi DNA, 17 sampel menghasilkan konsentrasi DNA sebesar 26,250-903,350 ng/µl pada kemurnian DNA sebesar 1,521-1,946. Hasil analisis DNA menggunakan primer 16E1/16E2 pada elektroforesis gel agaros, 16 sampel menunjukkan pita DNA sebesar 584 bp. Hasil uji mikrobiologi pada medium Endo Agar, 16 sampel positif E.coli dengan menunjukkan koloni merah metalik. Kontaminasi bakteri E.coli pada tempe segar diduga berasal dari proses produksi tidak dengan dua kali perebusan, lingkungan sekitar dan pekerja. Almost all phases in tempe production is critical stage, so it is need to apply the hygienic principle. This study attempts to identify the presence of Escherichia coli contamination in fresh tempe and to predict the possibility of factor that responsible in E.coli contamination in fresh tempe produced by tempe industry in Western Semarang. This research started with isolating DNA sample, and then analyzing the DNA with PCR method using 16E1/E2 primer, and later, microbiologically confirmation test using Endo Agar medium. The observation is conducted in 17 industries in Western Semarang. The results from isolating the DNA of 17 tempe samples produce DNA concentration of 26,250-903,350 ng/µl, while the DNA purity is 1,521-1,946. The results of DNA analysis using 16 E1/E2 primer showed that 16 tempe samples displayed DNA tape of 584 bp.The results of microbiologic test showed that 16 tempe samples positively E.coli-contaminated which identified by having a metallic pink colony in Endo Agar medium. Based on the results from observation, 16 industries is identified by having E.coli in the producted tempe because yet to apply hygienic production. As described above, E.coli contamination came from the environment, the worker, and the production process is not with boiling twice.

Collaboration network of the authors

40 authors · 88 co-authorship links · showing the 40 most connected

Hover or tap a name to highlight its co-authors. Double-click to open the author's page.

  • State University of Semarang
  • Diponegoro University
  • Universitas Indraprasta PGRI
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
  • Thicker line = more joint articles · bigger circle = more articles
Show as table
Co-authorOrganisationJoint articles
Pramesti DewiAffiliation unknown17
Ibnul MubarokAffiliation unknown5
Talitha WidiatningrumAffiliation unknown4
Andhina Putri HeriyantiDiponegoro University2
R. SusantiAffiliation unknown2
Mutiara Bintang RamadaniAffiliation unknown2
Astrid FarmayatiAffiliation unknown2
Lusi Maswahyu AndriyaniAffiliation unknown2
SunyotoAffiliation unknown2
Lidya Ayu NataliaAffiliation unknown2
Ruri WinantiAffiliation unknown2
Anis MaftuhahAffiliation unknown2
Nihayatul MilahAffiliation unknown2
Nikmatul HidayahAffiliation unknown2
Supriyadi SupriyadiAffiliation unknown1
Kusmuriyanto KusmuriyantoAffiliation unknown1
Mochamad Nur SholikhinAffiliation unknown1
Nishfa MufatihahAffiliation unknown1
Nadya Wulan RamadhaniAffiliation unknown1
Hasyim AbdurrasyidAffiliation unknown1
Ghani WalandipaAffiliation unknown1
Siti Harnina BintariAffiliation unknown1
Nilam SyifaAffiliation unknown1
Nana Kariada Tri MartutiState University of Semarang1
Fitria Ayu TirtaningrumAffiliation unknown1
Fahmi RahmawatiAffiliation unknown1
Retno Sri IswariState University of Semarang1
Septi JayantiAffiliation unknown1
Saeful AnhariAffiliation unknown1
Dwi SusilaningsihAffiliation unknown1
Aulia Nuanza AlamAffiliation unknown1
Sri UtamiUniversitas Indraprasta PGRI1
Yenni Tyas Wulandari K. EAffiliation unknown1
Ari YuniastutiState University of Semarang1
Intan Ayu ElissaAffiliation unknown1
Afra Fauziah L. PutriAffiliation unknown1
Nadya Audina Nurkhafiya SadikinAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://journal.unnes.ac.id/sju/index.php/UnnesJLifeSci/oai, first harvested 5 Nov 2026, last seen 5 Nov 2026.
Original metadata (oai_dc)
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	<dc:title xml:lang="en-US">ANALISIS PROSES PEMBUATAN TEMPE MELALUI CARA PRODUKSI HIGIENIS DAN PENDEKATAN MOLEKULER</dc:title>
	<dc:creator>Nugraini, Anisa Ratna</dc:creator>
	<dc:creator>Bintari, Siti Harnina</dc:creator>
	<dc:creator>Mustikaningtyas, Dewi</dc:creator>
	<dc:description xml:lang="en-US">Hampir semua tahapan pembuatan tempe merupakan tahap kritikal, sehingga dalam pembuatannya perlu menerapkan prinsip hieginis. Penelitian ini bertujuan untuk mengidentifikasi ada tidaknya kontaminasi bakteri Escherichia coli pada tempe segar dan untuk memprediksi kemungkinan faktor penyebab kontaminasi tersebut di sentra industri tempe Semarang Barat. Observasi dilakukan pada 17 industri tempe di Semarang Barat. Pengujian molekuler secara berturut-turut dilakukan dengan isolasi DNA, analisis DNA menggunakan primer 16E1/E2, dan uji mikrobiologi menggunakan medium Endo Agar. Berdasarkan hasil observasi, 16 industri tempe teridentifikasi ada bakteri E.coli. Satu industri tempe tidak teridentifikasi ada bakteri E.coli. Hal ini ada hubungannya terhadap diterapkannya cara produksi higienis. Hasil yang diperoleh dari isolasi DNA, 17 sampel menghasilkan konsentrasi DNA sebesar 26,250-903,350 ng/µl pada kemurnian DNA sebesar 1,521-1,946. Hasil analisis DNA menggunakan primer 16E1/16E2 pada elektroforesis gel agaros, 16 sampel menunjukkan pita DNA sebesar 584 bp. Hasil uji mikrobiologi pada medium Endo Agar, 16 sampel positif E.coli dengan menunjukkan koloni merah metalik. Kontaminasi bakteri E.coli pada tempe segar diduga berasal dari proses produksi tidak dengan dua kali perebusan, lingkungan sekitar dan pekerja.
&amp;nbsp;
Almost all phases in tempe production is critical stage, so it is need to apply the hygienic principle. This study attempts to identify the presence of Escherichia coli contamination in fresh tempe and to predict the possibility of factor that responsible in E.coli contamination in fresh tempe produced by tempe industry in Western Semarang. This research started with isolating DNA sample, and then analyzing the DNA with PCR method using 16E1/E2 primer, and later, microbiologically confirmation test using Endo Agar medium. The observation is conducted in 17 industries in Western Semarang. The results from isolating the DNA of 17 tempe samples produce DNA concentration of 26,250-903,350 ng/µl, while the DNA purity is 1,521-1,946. The results of DNA analysis using 16 E1/E2 primer showed that 16 tempe samples displayed DNA tape of 584 bp.The results of microbiologic test showed that 16 tempe samples positively E.coli-contaminated which identified by having a metallic pink colony in Endo Agar medium. Based on the results from observation, 16 industries is identified by having E.coli in the producted tempe because yet to apply hygienic production. As described above, E.coli contamination came from the environment, the worker, and the production process is not with boiling twice.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Negeri Semarang</dc:publisher>
	<dc:date>2017-02-28</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.unnes.ac.id/sju/UnnesJLifeSci/article/view/13183</dc:identifier>
	<dc:source xml:lang="en-US">Life Science; Vol 5 No 1 (2016): April 2016; 9-17</dc:source>
	<dc:source>2528-5009</dc:source>
	<dc:source>2252-6277</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.unnes.ac.id/sju/UnnesJLifeSci/article/view/13183/7246</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2016 Life Science</dc:rights>
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